Редактирование: COMP (раздел)

==Publications==

{{medline-entry
|title=Effect of circadian rhythm, age, training and acute lameness on serum concentrations of cartilage oligomeric matrix protein ([[COMP]]) neo-epitope in horses.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/30739342
|abstract=Molecular serum markers that can identify early reversible osteoarthritis (OA) in horses are lacking. We studied serum concentrations of a novel cartilage oligomeric matrix protein ([[COMP]]) neo-epitope in horses subjected to short-term exercise and with acute lameness. The effects of circadian rhythm and age were also evaluated. Longitudinal studies in healthy horses and cross-sectional comparison of lame and non-lame horses. Sera were collected from five horses before and after short-term interval exercise and during full-day box rest. Sera from 32 acutely lame horses were used to evaluate age-related effects. Independent samples from control horses (n = 41) and horses with acute lameness (n = 71) were included. [[COMP]] neo-epitope concentrations were analysed using custom-developed inhibition ELISAs validated for equine serum. The presence of [[COMP]] neo-epitope was delineated in healthy and osteoarthritic articular cartilage with immunohistochemistry. [[COMP]] neo-epitope concentrations decreased after speed training but returned to baseline levels post-exercise. No correlations between age and serum [[COMP]] neo-epitope concentrations were found (r = 0.0013). The mean (±s.d.) serum concentration of [[COMP]] neo-epitope in independent samples from non-lame horses was 0.84 ± 0.38 μg/mL, and for lame horses was 5.24 ± 1.83 μg/mL (P<0.001). Antibodies against [[COMP]] neo-epitope did not stain normal articular cartilage, but intracytoplasmic staining was found in superficial chondrocytes of mild OA cartilage and in the extracellular matrix of moderately osteoarthritic cartilage. ELISA was based on polyclonal antisera rather than a monoclonal antibody. There is a sex and breed bias within the groups of horses, also it could have been of value to include horses with septic arthritis and tendonitis and investigated joint differences. This [[COMP]] neo-epitope can be measured in sera, and results indicate that it could be a biomarker for pathologic fragmentation of cartilage in connection with acute joint lameness.
|mesh-terms=* Aging
* Animals
* Biomarkers
* Cartilage Oligomeric Matrix Protein
* Circadian Rhythm
* Epitopes
* Female
* Horse Diseases
* Horses
* Lameness, Animal
* Longitudinal Studies
* Male
* Physical Conditioning, Animal
|keywords=* COMP neo-epitope
* biomarker
* circadian
* horse
* lameness
* serum
* training
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6767518
}}
{{medline-entry
|title=Genetic overexpression of [[COMP]]-Ang1 impairs BM microenvironment and induces senescence of BM HSCs.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29604278
|abstract=Supplemental Angiopoietin 1 (Ang1) exerts its therapeutic potential on microvascular regression-associated diseases, and this potential is linked with the function of hematopoietic stem cells (HSCs). However, the underlying mechanisms of the effect of enhanced angiogenesis on the modulation of HSCs are not yet defined. Here, we generated transgenic mice expressing Cartilage Oligomeric Matrix Protein ([[COMP]])-Ang1 in keratin 14-expressing cells. The mutant animals expressed excessive angiogenic characteristics in the skin and bone marrow (BM) along with redder skin with more numerous and branched vessels compared with their wild-type (WT) littermates. The mutants displayed reduced long bone formation and osteoclast activity than did WT littermates and had fewer CD150 [[CD48]] Lineage Sca-1 c-Kit  (LSK) cells in the BM. The mutants also exhibited greater senescence-associated (SA) β-gal activity, p16  protein expression, and superoxide anion levels in CD150 [[CD48]] LSK cells in the BM. Furthermore, transplantation assay revealed that the mutant-derived LSK cells were inferior to the cells derived from WT littermate in inducing competitive repopulating capacity in the recipients. Collectively, our results demonstrate that persistent and prolonged administration of [[COMP]]-Ang1 by inducible transgenic expression mediates excessive angiogenesis in the body and impairs BM microenvironment, eventually leading to senescence of BM HSCs.
|mesh-terms=* Angiopoietin-1
* Animals
* Bone Marrow
* Cartilage Oligomeric Matrix Protein
* Cellular Microenvironment
* Cellular Senescence
* Gene Expression
* Hematopoietic Stem Cells
* Humans
* Mice, Transgenic
* Mutation
* Neovascularization, Physiologic
* Osteoclasts
* Recombinant Fusion Proteins
|keywords=* Angiogenesis
* Bone marrow
* COMP-Ang1
* Hematopoietic stem cells
* Senescence
|full-text-url=https://sci-hub.do/10.1016/j.bbrc.2018.03.210
}}
{{medline-entry
|title=Longitudinal Twin Study of Subjective Health: Differences in Genetic and Environmental Components of Variance Across Age and Sex.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/29590493
|abstract=The current analysis examines sex differences in longitudinal changes in genetic and environmental influences on three measures of subjective health (SH). Sample includes 7,372 twins (mean intake age = 73.22) with up to 8 waves of measurement (mean = 3.1). Three SH items were included: general self-rated health (SRH), health compared to age peers ([[COMP]]), and impact of health on activities (ACT) which previous research shows capture different frames of reference. Latent growth curve modeling indicated significant differences across gender and frame of reference in trajectories of change with age and in genetic and environmental contributions to change. Men have higher mean scores on all three SH measures, indicating better SH, but there were no sex differences in pattern of change with age. Accelerating declines with age were found for SRH and ACT, whereas [[COMP]] improved with age. Results indicated more genetic variance for women than men, but declining genetic variance for both after age 70. Increasing shared environmental variance with increasing age was also found for both sexes. As aging triggers a re-evaluation of the meaning of "good health," physical aspects of health may become less important and shared cultural conceptions of health may become more relevant. This change in conceptions of good health may reflect both aging and the change in composition of the elderly population as a result of selective survival.
|mesh-terms=* Activities of Daily Living
* Adult
* Aged
* Aged, 80 and over
* Aging
* Attitude to Health
* Diagnostic Self Evaluation
* Female
* Health Status
* Humans
* Longitudinal Studies
* Male
* Middle Aged
* Peer Group
* Sex Factors
|keywords=* Frame of reference
* Latent growth curve model
* Question type
* Self-rated health
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6909438
}}
{{medline-entry
|title=Cartilage biomarkers in the osteoarthropathy of alkaptonuria reveal low turnover and accelerated ageing.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/28028161
|abstract=Alkaptonuria (AKU) is a rare autosomal recessive disease resulting from a single enzyme deficiency in tyrosine metabolism. As a result, homogentisic acid cannot be metabolized, causing systemic increases. Over time, homogentisic acid polymerizes and deposits in collagenous tissues, leading to ochronosis. Typically, this occurs in joint cartilages, leading to an early onset, rapidly progressing osteoarthropathy. The aim of this study was to examine tissue turnover in cartilage affected by ochronosis and its role in disease initiation and progression. With informed patient consent, hip and knee cartilages were obtained at surgery for arthropathy due to AKU (n = 6; 2 knees/4 hips) and OA (n = 12; 5 knees/7 hips); healthy non-arthritic (non-OA n = 6; 1 knee/5 hips) cartilages were obtained as waste from trauma surgery. We measured cartilage concentrations (normalized to dry weight) of racemized aspartate, GAG, [[COMP]] and deamidated [[COMP]] (D-[[COMP]]). Unpaired AKU, OA and non-OA samples were compared by non-parametric Mann-Whitney U test. Despite more extractable total protein being obtained from AKU cartilage than from OA or non-OA cartilage, there was significantly less extractable GAG, [[COMP]] and D-[[COMP]] in AKU samples compared with OA and non-OA comparators. Racemized Asx (aspartate and asparagine) was significantly enriched in AKU cartilage compared with in OA cartilage. These novel data represent the first examination of cartilage matrix components in a sample of patients with AKU, representing almost 10% of the known UK alkaptonuric population. Compared with OA and non-OA, AKU cartilage demonstrates a very low turnover state and has low levels of extractable matrix proteins.
|mesh-terms=* Adult
* Aged
* Aged, 80 and over
* Aging
* Alkaptonuria
* Aspartic Acid
* Biomarkers
* Cartilage Oligomeric Matrix Protein
* Cartilage, Articular
* Case-Control Studies
* Female
* Glycosaminoglycans
* Hip Joint
* Humans
* Joint Diseases
* Knee Joint
* Male
* Middle Aged
* Ochronosis
* Osteoarthritis, Hip
* Osteoarthritis, Knee
* Young Adult
|keywords=* ageing
* alkaptonuria
* biomarkers
* cartilage oligomeric matrix protein
* glycosaminoglycan
* ochronosis
* osteoarthritis
* racemization
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5188995
}}
{{medline-entry
|title=Scleraxis Is Essential for Tendon Differentiation by Equine Embryonic Stem Cells and in Equine Fetal Tenocytes.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/27899062
|abstract=The transcription factor scleraxis is required for tendon development and is upregulated during embryonic stem cell (ESC) differentiation into tenocytes. However, its role beyond early embryonic development is not defined. We utilized a short hairpin RNA to knock down scleraxis expression in ESCs and adult and fetal tenocytes. No effect on growth or morphology was observed in two-dimensional cultures. However, scleraxis knockdown in fetal tenocytes significantly reduced [[COL1A1]], [[COMP]], and [[SOX9]] gene expression. Scleraxis knockdown in adult tenocytes had no effect on the expression of these genes. Strikingly, differentiating ESCs and fetal tenocytes without scleraxis failed to reorganize a three-dimensional (3D) matrix and generate artificial tendons. This was associated with a significantly reduced survival. In contrast, there was no effect on the survival and remodeling capacity of adult tenocytes following scleraxis knockdown. Overexpression of scleraxis in fetal tenocytes rescued gene expression, cell survival in 3D, and subsequent matrix contraction. Together, these results demonstrate that scleraxis is not only essential for ESC differentiation into tenocytes but that it also has an active role in maintaining fetal tenocytes, which is then redundant in adult tenocytes.
|mesh-terms=* Aging
* Animals
* Basic Helix-Loop-Helix Transcription Factors
* Cartilage Oligomeric Matrix Protein
* Cell Differentiation
* Cell Proliferation
* Cell Survival
* Cells, Cultured
* Collagen Type I
* DNA, Complementary
* Embryonic Stem Cells
* Fetus
* Gels
* Gene Expression Regulation
* Gene Knockdown Techniques
* Horses
* RNA, Small Interfering
* SOX9 Transcription Factor
* Tendons
* Tenocytes
|keywords=* embryonic stem cells
* scleraxis
* tendon
|full-text-url=https://sci-hub.do/10.1089/scd.2016.0279
}}
{{medline-entry
|title=Cartilage oligomeric matrix protein prevents vascular aging and vascular smooth muscle cells senescence.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/27498005
|abstract=Aging-related vascular dysfunction contributes to cardiovascular morbidity and mortality. Cartilage oligomeric matrix protein ([[COMP]]), a vascular extracellular matrix protein, has been described as a negative regulatory factor for the vascular aging-related processes including atherosclerosis and vascular calcification. However, whether [[COMP]] is implicated in the process of vascular aging remains unclear. Here, we identified a novel function of [[COMP]] in preventing vascular aging and vascular smooth muscle cells (VSMCs) senescence. Firstly, vascular [[COMP]] expression was decreased in three different senescence-accelerated mouse models and was also declining with age. [[COMP]](-/-) mice displayed elevated senescence-associated markers expression, including p53, p21 and p16, in the aortas compared with their wild type (WT) littermates. In accordance, [[COMP]] deficiency induced aging-related vascular dysfunction as evidenced by the significantly reduced phenylephrine-induced contraction and increased vascular stiffness as evaluated by pulse wave velocity. The aortic wall of [[COMP]](-/-) mice was susceptible to senescence by displaying senescence-associated β-galactosidase (SA β-gal) activity induced by periadventitial application of CaCl2 to the abdominal aorta. In vitro, [[COMP]] knockdown by small interfering (si) RNA led to the elevation of p53, p21 and p16 as well as SA β-gal activity in VSMCs after H2O2 stimulation. VSMCs isolated from [[COMP]](-/-) mice showed elevated senescence-associated markers expression and supplement of [[COMP]] adenovirus to [[COMP]]-deficient VSMCs greatly rescued cellular senescence. Taken together, these findings revealed the essential role of [[COMP]] in retarding the development of vascular aging and VSMC senescence.
|mesh-terms=* Aging
* Animals
* Aorta
* Blood Vessels
* Cartilage Oligomeric Matrix Protein
* Cellular Senescence
* Mice, Inbred C57BL
* Models, Animal
* Muscle, Smooth, Vascular
* Myocytes, Smooth Muscle
* Rats
|keywords=* COMP
* VSMC senescence
* Vascular aging
* Vascular extracellular matrix protein
|full-text-url=https://sci-hub.do/10.1016/j.bbrc.2016.08.004
}}
{{medline-entry
|title=Fibrotic-like changes in degenerate human intervertebral discs revealed by quantitative proteomic analysis.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/26463451
|abstract=Intervertebral disc degeneration (IDD) can lead to symptomatic conditions including sciatica and back pain. The purpose of this study is to understand the extracellular matrix (ECM) changes in disc biology through comparative proteomic analysis of degenerated and non-degenerated human intervertebral disc (IVD) tissues of different ages. Seven non-degenerated (11-46 years of age) and seven degenerated (16-53 years of age) annulus fibrosus (AF) and nucleus pulposus (NP) samples were used. Proteins were extracted using guanidine hydrochloride, separated from large proteoglycans (PGs) by caesium chloride (CsCl) density gradient ultracentrifugation, and identified using liquid chromatography (LC) coupled with tandem mass spectrometry (MS/MS). For quantitative comparison, proteins were labeled with iTRAQ reagents. Collagen fibrils in the NP were assessed using scanning electron microscopy (SEM). In the AF, quantitative analysis revealed increased levels of [[HTRA1]], [[COMP]] and [[CILP]] in degeneration when compared with samples from older individuals. Fibronectin showed increment with age and degeneration. In the NP, more [[CILP]] and [[CILP]]2 were present in degenerated samples of younger individuals. Reduced protein solubility was observed in degenerated and older non-degenerated samples correlated with an accumulation of type I collagen in the insoluble fibers. Characterization of collagen fibrils in the NP revealed smaller mean fibril diameters and decreased porosity in the degenerated samples. Our study identified distinct matrix changes associated with aging and degeneration in the intervertebral discs (IVDs). The nature of the ECM changes, together with observed decreased in solubility and changes in fibril diameter is consistent with a fibrotic-like environment.
|mesh-terms=* Adolescent
* Adult
* Aging
* Child
* Collagen
* Fibrosis
* Humans
* Intervertebral Disc
* Intervertebral Disc Degeneration
* Microscopy, Electron, Scanning
* Middle Aged
* Nucleus Pulposus
* Proteins
* Proteomics
* Solubility
* Young Adult
|keywords=* Disc degeneration
* Fibrosis
* Intervertebral disc
* Mass spectrometry
* Proteome
* Quantitative method
|full-text-url=https://sci-hub.do/10.1016/j.joca.2015.09.020
}}
{{medline-entry
|title=Enhanced tissue regeneration potential of juvenile articular cartilage.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/24043472
|abstract=Articular cartilage undergoes substantial age-related changes in molecular composition, matrix structure, and mechanical properties. These age-related differences between juvenile and adult cartilage manifest themselves as markedly distinct potentials for tissue repair and regeneration. To compare the biological properties and tissue regeneration capabilities of juvenile and adult bovine articular cartilage. Controlled laboratory study. Articular cartilage harvested from juvenile (age, 4 months) and adult (age, 6-8 years) bovine femoral condyles was cultured for 4 weeks to monitor chondrocyte migration, glycosaminoglycan content conservation, and new tissue formation. The cartilage cell density and proliferative activity were also compared. Additionally, the effects of age-related changes on cartilage gene expression were analyzed using the Affymetrix GeneChip array. Compared with adult cartilage, juvenile bovine cartilage demonstrated a significantly greater cell density, higher cell proliferation rate, increased cell outgrowth, elevated glycosaminoglycan content, and enhanced matrix metallopeptidase 2 activity. During 4 weeks in culture, only juvenile cartilage was able to generate new cartilaginous tissues, which exhibited pronounced labeling for proteoglycan and type II collagen but not type I collagen. With over 19,000 genes analyzed, distinctive gene expression profiles were identified. The genes mostly involved in cartilage growth and expansion, such as [[COL2A1]], [[COL9A1]], [[MMP2]], [[MMP14]], and [[TGFB3]], were upregulated in juvenile cartilage, whereas the genes primarily responsible for structural integrity, such as [[COMP]], [[FN1]], [[TIMP2]], [[TIMP3]], and [[BMP2]], were upregulated in adult cartilage. As the first comprehensive comparison between juvenile and adult bovine articular cartilage at the tissue, cellular, and molecular levels, the results strongly suggest that juvenile cartilage possesses superior chondrogenic activity and enhanced regenerative potential over its adult counterpart. Additionally, the differential gene expression profiles of juvenile and adult cartilage suggest possible mechanisms underlying cartilage age-related changes in their regeneration capabilities, structural components, and biological properties. The results of this comparative study between juvenile and adult bovine articular cartilage suggest an enhanced regenerative potential of juvenile cartilage tissue in the restoration of damaged articular cartilage.
|mesh-terms=* Aging
* Animals
* Cartilage, Articular
* Cattle
* Cell Count
* Cell Proliferation
* Chondrocytes
* Gene Expression Profiling
* Glycosaminoglycans
* Matrix Metalloproteinase 2
* Oligonucleotide Array Sequence Analysis
* Regeneration
|keywords=* adult
* aging
* articular cartilage
* biology of cartilage
* bovine
* cartilage regeneration
* cartilage repair
* chondrocyte
* gene expression
* juvenile
* knee
* migration
|full-text-url=https://sci-hub.do/10.1177/0363546513502945
}}
{{medline-entry
|title=Abnormal bone quality in cartilage oligomeric matrix protein and matrilin 3 double-deficient mice caused by increased tissue inhibitor of metalloproteinases 3 deposition and delayed aggrecan degradation.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/22378539
|abstract=Cartilage oligomeric matrix protein ([[COMP]]) and matrilin 3 are extracellular matrix proteins that are abundant in cartilage. As adaptor molecules, both proteins bridge and stabilize macromolecular networks consisting of fibrillar collagens and proteoglycans. Mutations in the genes coding for [[COMP]] and matrilin 3 have been linked to human chondrodysplasias, while in mice, deficiency in [[COMP]] or matrilin 3 does not cause any pronounced skeletal abnormalities. Given the similar functions of [[COMP]] and matrilin 3 in the assembly and stabilization of the extracellular matrix, our aim was to determine whether these proteins could functionally compensate for each other. To assess this putative redundancy of [[COMP]] and matrilin 3, we generated [[COMP]]/matrilin 3 double-deficient mice and performed an in-depth analysis of their skeletal development. At the newborn stage, the overall skeletal morphology of the double mutants was normal, but at 1 month of age, the long bones were shortened and the total body length reduced. Peripheral quantitative computed tomography revealed increased metaphyseal trabecular bone mineral density in the femora. Moreover, the degradation of aggrecan in the cartilage remnants in the metaphyseal trabecular bone was delayed, paralleled by increased deposition of tissue inhibitor of metalloproteinases 3 (TIMP-3). The structure and morphology of the growth plate were grossly normal, but in the center, focal closures were observed, a phenotype very similar to that described in matrix metalloproteinase 13 (MMP-13)-deficient mice. We propose that a lack of [[COMP]] and matrilin 3 leads to increased deposition of TIMP-3, which causes partial inactivation of MMPs, including MMP-13, a mechanism that would explain the similarities in phenotype between [[COMP]]/matrilin 3 double-deficient and MMP-13-deficient mice.
|mesh-terms=* Aggrecans
* Aging
* Animals
* Animals, Newborn
* Bone Density
* Bone and Bones
* Cartilage Oligomeric Matrix Protein
* Extracellular Matrix Proteins
* Glycoproteins
* Matrilin Proteins
* Mice
* Mice, Inbred C57BL
* Mice, Knockout
* Models, Animal
* Phenotype
* Tissue Inhibitor of Metalloproteinase-3

|full-text-url=https://sci-hub.do/10.1002/art.34435
}}
{{medline-entry
|title=Variations in gene and protein expression in human nucleus pulposus in comparison with annulus fibrosus and cartilage cells: potential associations with aging and degeneration.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/19833252
|abstract=Regardless of recent progress in the elucidation of intervertebral disc ([[IVD]]) degeneration, the basic molecular characteristics that define a healthy human [[IVD]] are largely unknown. Although work in different animal species revealed distinct molecules that might be used as characteristic markers for [[IVD]] or specifically nucleus pulposus (NP) cells, the validity of these markers for characterization of human [[IVD]] cells remains unknown. Eleven potential marker molecules were characterized with respect to their occurrence in human [[IVD]] cells. Gene expression levels of NP were compared with annulus fibrosus (AF) and articular cartilage (AC) cells, and potential correlations with aging were assessed. Higher mRNA levels of cytokeratin-19 ([[KRT19]]) and of neural cell adhesion molecule-1 were noted in NP compared to AF and AC cells. Compared to NP cytokeratin-18 expression was lower in AC, and alpha-2-macroglobulin and desmocollin-2 lower in AF. Cartilage oligomeric matrix protein ([[COMP]]) and glypican-3 expression was higher in AF, while [[COMP]], matrix gla protein ([[MGP]]) and pleiotrophin expression was higher in AC cells. Furthermore, an age-related decrease in [[KRT19]] and increase in [[MGP]] expression were observed in NP cells. The age-dependent expression pattern of [[KRT19]] was confirmed by immunohistochemistry, showing the most prominent [[KRT19]] immunoreaction in the notochordal-like cells in juvenile NP, whereas [[MGP]] immunoreactivity was not restricted to NP cells and was found in all age groups. The gene expression of [[KRT19]] has the potential to characterize human NP cells, whereas [[MGP]] cannot serve as a characteristic marker. [[KRT19]] protein expression was only detected in NP cells of donors younger than 54 years.
|mesh-terms=* Adult
* Age Factors
* Aged
* Aged, 80 and over
* Aging
* Biomarkers
* Cartilage, Articular
* Chondrocytes
* Extracellular Matrix Proteins
* Female
* Fibrocartilage
* Gene Expression
* Humans
* Intervertebral Disc
* Male
* Middle Aged
* Phenotype
* Polymerase Chain Reaction
* Statistics as Topic
* Young Adult

|full-text-url=https://sci-hub.do/10.1016/j.joca.2009.09.009
}}
{{medline-entry
|title=Differential gene expression associated with postnatal equine articular cartilage maturation.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/18986532
|abstract=Articular cartilage undergoes an important maturation process from neonate to adult that is reflected by alterations in matrix protein organization and increased heterogeneity of chondrocyte morphology. In the horse, these changes are influenced by exercise during the first five months of postnatal life. Transcriptional profiling was used to evaluate changes in articular chondrocyte gene expression during postnatal growth and development. Total RNA was isolated from the articular cartilage of neonatal (0-10 days) and adult (4-5 years) horses, subjected to one round of linear RNA amplification, and then applied to a 9,367-element equine-specific cDNA microarray. Comparisons were made with a dye-swap experimental design. Microarray results for selected genes (COL2A1, [[COMP]], [[P4HA1]], [[TGFB1]], [[TGFBR3]], TNC) were validated by quantitative polymerase chain reaction (qPCR). Fifty-six probe sets, which represent 45 gene products, were up-regulated (p < 0.01) in chondrocytes of neonatal articular cartilage relative to chondrocytes of adult articular cartilage. Conversely, 586 probe sets, which represent 499 gene products, were up-regulated (p < 0.01) in chondrocytes of adult articular cartilage relative to chondrocytes of neonatal articular cartilage. Collagens, matrix-modifying enzymes, and provisional matrix non-collagenous proteins were expressed at higher levels in the articular cartilage of newborn foals. Those genes with increased mRNA abundance in adult chondrocytes included leucine-rich small proteoglycans, matrix assembly, and cartilage maintenance proteins. Differential expression of genes encoding matrix proteins and matrix-modifying enzymes between neonates and adults reflect a cellular maturation process in articular chondrocytes. Up-regulated transcripts in neonatal cartilage are consistent with growth and expansion of the articular surface. Expression patterns in mature articular cartilage indicate a transition from growth to homeostasis, and tissue function related to withstanding shear and weight-bearing stresses.
|mesh-terms=* Aging
* Animals
* Cartilage, Articular
* Chondrocytes
* Collagen Type II
* Extracellular Matrix Proteins
* Gene Expression Profiling
* Gene Expression Regulation, Developmental
* Growth
* Homeostasis
* Horses
* Intercellular Signaling Peptides and Proteins
* Proteoglycans
* RNA, Messenger
* Receptors, Transforming Growth Factor beta
* Tenascin
* Transforming Growth Factor beta1
* Up-Regulation
* Weight-Bearing

|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2585085
}}
{{medline-entry
|title=Ablation of collagen IX and [[COMP]] disrupts epiphyseal cartilage architecture.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/18191556
|abstract=Chondrodysplasias are a genetically heterogeneous group of skeletal disorders. Mutations in genes coding for cartilage oligomeric matrix protein ([[COMP]]), collagen IX and matrilin-3 have been described to cause the autosomal dominantly inherited form of multiple epiphyseal dysplasia (MED). Even though there is clear evidence that these cartilage matrix proteins interact with each other, their exact functions in matrix organisation and bone development still need to be elucidated. We generated a mouse model lacking both collagen IX and [[COMP]] to study the potential complementary role of these proteins in skeletal development. Mice deficient in both proteins exhibit shortened and widened long bones as well as an altered bone structure. They display severe growth plate abnormalities with large hypocellular areas in the central parts of the tibia. In addition, chondrocytes in the proliferative and hypertrophic zones do not show their typical columnar arrangement. These phenotypical traits were not observed in mice deficient only in [[COMP]], while mice lacking only collagen IX showed similar growth plate disturbances and shorter and wider tibiae. The contribution of [[COMP]] to the phenotype of mice deficient in both collagen IX and [[COMP]] appears minor, even though clear differences in the deposition of matrilin-3 were detected.
|mesh-terms=* Aging
* Animals
* Body Patterning
* Bone and Bones
* Collagen Type IX
* Extracellular Matrix Proteins
* Gene Expression Regulation, Developmental
* Glycoproteins
* Growth Plate
* Matrilin Proteins
* Mice
* Mice, Inbred C57BL
* Mice, Knockout

|full-text-url=https://sci-hub.do/10.1016/j.matbio.2007.11.007
}}
{{medline-entry
|title=Ultrastructural immunolocalization of cartilage oligomeric matrix protein ([[COMP]]) in relation to collagen fibrils in the equine tendon.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/16005620
|abstract=The structure and organisation of the extracellular matrix, and in particular the axial alignment of type I collagen fibrils, are essential for the tensile strength of tendons. The resident tenocytes synthesize and maintain the composition of the extracellular matrix, which changes with age and maturation. Other components of the extracellular matrix include less abundant collagen types II, III, V, VI, XII, proteoglycans and glycoproteins. Cartilage oligomeric matrix protein ([[COMP]]) is an abundant non-collagenous pentameric glycoprotein in the tendon, which can bind to collagen types I and II. The function of [[COMP]] in the tendon is not clear, but it may act as a catalyst in fibrillogenesis. Its concentration changes with age, maturation and load. The present study delineates the ultrastructural distribution of [[COMP]] and its correlation to collagen fibril thickness in different compartments in two flexor tendons from horses of different ages (foetus, 8 months, 3 years, 12 years). The immunolabeling for [[COMP]] was higher in the superficial digital flexor tendon compared with the deep digital flexor tendon and it increased with the age of the animal, with the highest concentration in the 3-year-olds. Fibril diameter differed between age groups and a more homogenous fibril population was found in the fetal tendons. A positive correlation between high [[COMP]] immunolabeling and the percentage of small fibrils (<60 nm) were present in the SDFT. [[COMP]] immunolabeling was enriched at the gap region of the collagen fibril. In situ hybridization revealed the strongest expression in tendons from the 3-year-old horses whereas there was no expression in foetal tendon.
|mesh-terms=* Aging
* Animals
* Collagen Type I
* Extracellular Matrix Proteins
* Glycoproteins
* Horses
* Immunochemistry
* In Situ Hybridization
* Matrilin Proteins
* Microscopy, Electron
* Tendons

|full-text-url=https://sci-hub.do/10.1016/j.matbio.2005.06.003
}}
{{medline-entry
|title=Sperm chromatin stability in frozen-thawed semen is maintained over age in AI bulls.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/15763115
|abstract=The aim of the present study was to investigate the effect of age of the sire on the in vitro quality of frozen-thawed (FT) bull spermatozoa, both when tested immediately postthaw (PT) and when assessed after cleansing and selection through a swim-up (SU) procedure. Semen samples from six Swedish Red and White Breed (SRB) artificial insemination (AI) bulls at age 1 and again, at 4 years were collected and frozen in 0.25 ml plastic straws. Also, semen was collected from six Estonian Holstein ([[EHF]]) bulls at the ages of 3, 5, and 7 years and likewise processed. The FT semen was tested for the susceptibility of sperm nuclear deoxyribonucleic acid (DNA) to undergo acid-induced denaturation in situ, as quantified by flow cytometry (FCM). The DNA denaturability was expressed as function alpha t, i.e., as the ratio of red (denaturated DNA) to red   green (total cellular DNA) fluorescence intensity. The results were expressed as the percentage of cells with high alpha t values, i.e., cells outside the main population (% [[COMP]] alpha t). Morphological evaluation of the same samples was performed to detect general and sperm head abnormalities and differences between ages. Fertility results were available as non-return rates (NRRs) for the semen of the sires when they were 1 year (SRB) and 3 years ([[EHF]]) old, varying from 62.2 to 70.7% in SRB and from 52.2 to 76.0% in [[EHF]] animals. The [[COMP]] alpha t values ranged from 0.5-3.6% (PT) to 0.2-1.7% (SU) for SRB bulls and from 0.4-1.8% (PT) to 0.2-1.5% (SU) for [[EHF]] bulls. Both breeds lacked differences between ages, either PT or after SU. However, the SU procedure yielded a significantly higher population of spermatozoa with stable DNA following acid-induced denaturation, than PT samples (p < 0.001). No correlation was detected between field fertility and chromatin stability. The results indicate that for these bull populations, the SU procedure was able to select spermatozoa with stable chromatin from the bulk samples. However, the use of DNA denaturation as a challenge to assess sperm chromatin stability did not offer a more accurate tool to evaluate sperm quality than the conventional, light microscopical evaluation of morphology.
|mesh-terms=* Aging
* Animals
* Cattle
* Chromatin
* Cryopreservation
* DNA
* Drug Stability
* Fertility
* Hot Temperature
* Insemination, Artificial
* Male
* Nucleic Acid Denaturation
* Semen Preservation
* Sensitivity and Specificity
* Spermatozoa

|full-text-url=https://sci-hub.do/10.1016/j.theriogenology.2004.08.001
}}
{{medline-entry
|title=Tenocyte response to cyclical strain and transforming growth factor beta is dependent upon age and site of origin.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/15477668
|abstract=The effect of strain and transforming growth factor beta on equine tendon fibroblasts (tenocytes) was assessed in vitro. Tenocytes were isolated from flexor and extensor tendons of horses from foetal to 10 years of age. These cells were cultured until confluent on collagen-coated silicone dishes. Cyclic biaxial strain of 9 /-1% was applied at 0.5 Hz for 24 hours with or without added TGFbeta1 or 3 (10 ng/ml). Proliferation and synthetic responses were dependent on the tendon of origin. Neither strain nor TGFbeta caused flexor tenocytes to proliferate significantly, while strain alone did proliferate extensor tenocytes. TGFbeta, with or without strain, increased the incorporation of [3H]-proline and the production of types I and III collagen and [[COMP]] in both cell types, although the effect on [[COMP]] production was more marked in flexor tenocytes, perhaps reflecting the higher levels found in this tendon in vivo. Immature flexor tenocytes synthesised more collagen and [[COMP]] than those from mature animals, while age had little effect in extensor tenocytes. Our results suggest that tenocytes become differentiated at an early age and present tendon-specific responses.
|mesh-terms=* Aging
* Animals
* Cell Differentiation
* Cell Proliferation
* Cells, Cultured
* Collagen Type I
* Collagen Type III
* Extracellular Matrix Proteins
* Fibroblasts
* Glycoproteins
* Horses
* Matrilin Proteins
* Stress, Mechanical
* Tendons
* Transforming Growth Factor beta


}}
{{medline-entry
|title=Laboratory investigations in osteoarthritis.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/14703003
|abstract=Progress in the knowledge of pathogenic mechanisms and a better definition of the disease, together with the availability of new technologies, have recently improved the value of laboratory investigations in osteoarthritis (OA). The main objectives of these findings are early diagnosis, assessment of disease activity and severity, and evaluation of therapeutic effects. In this context, biochemical markers are potentially useful, as they are non-invasive and non-expansive. However, among the numerous substances increasingly proposed for these purposes, very few may be considered as true disease markers in OA; [[COMP]], antigenic keratan sulphate, hyaluronic acid, YKL-40, type III collagen N-propeptide and urinary glucosyl-galactosyl pyridinoline seem to be the most promising. However, serum or urinary determinations of these molecules are difficult to interpret adequately, due to their complex metabolism. Careful analysis of synovial fluid, mainly directed to leukocyte count and crystal detection, is still essential for diagnosis, but also for the evaluation of the levels of important markers of local inflammation, such as metalloproteinases and cytokines, which seem to be crucial in the pathogenesis of OA.
|mesh-terms=* Aging
* Humans
* Osteoarthritis
* Severity of Illness Index

|full-text-url=https://sci-hub.do/10.1007/BF03327358
}}
{{medline-entry
|title=Correlation of cartilage oligomeric matrix protein ([[COMP]]) levels in equine tendon with mechanical properties: a proposed role for [[COMP]] in determining function-specific mechanical characteristics of locomotor tendons.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/12405694
|abstract=Over-strain injury of the superficial digital flexor tendon (SDFT) is a common injury in the horse. Tendon appears to adapt to loads placed on it during development, but fatigue damage accumulates after skeletal maturity, which is inadequately repaired and predisposes to clinical tendinitis. In any population of horses, there is a wide variation in SDFT mechanical properties. A noncollagenous protein, cartilage oligomeric matrix protein ([[COMP]]), is particularly abundant during growth in the equine SDFT and has been proposed to have an organisational role in the formation of collagenous matrices. This study aimed to determine whether [[COMP]] levels were correlated to mechanical properties at skeletal maturity. Tendons from 2 groups of 12 horses were analysed: Group 1 horses with restricted age, 2 years  /- 2 months, showed a significant correlation between both ultimate tensile stress modulus of elasticity and stiffness and [[COMP]], while Group 2 mature horses with varying age did not, because of age- and exercise-induced loss of [[COMP]]. These data supports the hypothesis that [[COMP]] is an important mediator in the growth of tendon. This data would suggest that the identification of low [[COMP]] levels in tendon during growth would indicate horses prone to tendon injury and methods of promoting [[COMP]] synthesis during growth would potentially improve tendon quality and reduce the risk of subsequent tendinitis.
|mesh-terms=* Age Factors
* Aging
* Animals
* Cartilage
* Extracellular Matrix Proteins
* Glycoproteins
* Horse Diseases
* Horses
* Locomotion
* Matrilin Proteins
* Tendinopathy
* Tendon Injuries
* Tendons
* Tensile Strength
* Weight-Bearing

|full-text-url=https://sci-hub.do/10.1111/j.2042-3306.2002.tb05426.x
}}
{{medline-entry
|title=The distribution of cartilage oligomeric matrix protein ([[COMP]]) in tendon and its variation with tendon site, age and load.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/9501326
|abstract=A protein prominent in guanidine hydrochloride extracts of adult bovine and equine digital flexor tendons was confirmed to be Cartilage Oligomeric Matrix Protein ([[COMP]]) by non-reducing and reducing [[SDS]]-PAGE, reaction with rabbit anti-[[COMP]] polyclonal antiserum on Western blots, trypsin digestion followed by HPLC on a C2/C18 column, and identification of [[COMP]] mRNA from tendon on Northern blots. Immunohistochemistry and Western blots of extracts showed [[COMP]] to be present in all regions of digital flexor tendons. Equine tendon [[COMP]] was purified by ion exchange chromatography and gel filtration and used in a heterologous inhibition ELISA to quantify [[COMP]] in equine digital flexor tendons at different ages, and in other tendons and ligaments. Mean [[COMP]] levels in digital flexor tendon were approximately 2-5mg/g wet weight, but they showed a large variation. Levels were low in neonatal tendon but rose rapidly during growth, with the metacarpal (tensional) superficial digital flexor tendon having the highest levels (approximately 10mg/g wet weight). Levels subsequently declined in this region, while in areas which experience a variable amount of compression, levels increased less but then remained constant. Extensor tendons and collateral ligaments, which experience less loading in vivo, had levels similar to those in neonatal tendon. [[COMP]] was identified in scarred skin and granulation tissue but not in normal skin, chronic fibrosis, or a fibrosarcomatous skin growth. A unilateral non-weight-bearing growing animal contained three to six times more [[COMP]] in the weight-bearing digital flexor tendons compared to the paralyzed limb, while the extensor tendons had similar amounts in both limbs. With the recent discovery of a [[COMP]] gene mutation causing pseudoachondroplasia (Hecht et al., 1995), in which lax tendons and ligaments are a feature, the present data suggest that [[COMP]] is synthesized in response to, and is necessary for tendon to resist, load.
|mesh-terms=* Aging
* Animals
* Blotting, Northern
* Blotting, Western
* Cartilage
* Cattle
* Electrophoresis, Polyacrylamide Gel
* Enzyme-Linked Immunosorbent Assay
* Extracellular Matrix Proteins
* Glycoproteins
* Guanidine
* Horses
* Immunohistochemistry
* Matrilin Proteins
* Organ Size
* Tendons
* Weight-Bearing

|full-text-url=https://sci-hub.do/10.1016/s0945-053x(97)90014-7
}}
{{medline-entry
|title=Cartilage oligomeric matrix protein ([[COMP]]) is an abundant component of tendon.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/7957930
|abstract=An abundant matrix protein was purified under native conditions from adult bovine tendon and identified as cartilage oligomeric matrix protein ([[COMP]]) by immunochemical crossreaction, amino acid sequence identity of tryptic peptides derived from both N- and C-terminal regions, and structure revealed by electron microscopy. Immunohistochemistry showed age-dependent differences in distribution of [[COMP]] in tendon.
|mesh-terms=* Aging
* Amino Acid Sequence
* Animals
* Cartilage, Articular
* Cattle
* Extracellular Matrix Proteins
* Glycoproteins
* Immunoenzyme Techniques
* Matrilin Proteins
* Membrane Proteins
* Microscopy, Electron
* Molecular Sequence Data
* Molecular Weight
* Peptide Fragments
* Sequence Homology
* Tendons
* Trypsin

|full-text-url=https://sci-hub.do/10.1016/0014-5793(94)01134-6
}}
{{medline-entry
|title=Heterogeneity of sperm nuclear chromatin structure and its relationship to bull fertility.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/3593856
|abstract=The relationship between sperm nuclear chromatin structure and fertility was evaluated in two groups of Holstein bulls: Group 1, 49 mature bulls, and Group 2, 18 young bulls. Fertility ratings had been estimated for Group 1 and nonreturn rates were known for Group 2. Semen samples were measured by the sperm chromatin structure assay (SCSA): sperm were treated to induce partial in situ DNA denaturation, stained with acridine orange, and evaluated by flow cytometry. Acridine orange intercalated into double-stranded DNA emits green fluorescence upon excitation with 488 nm light, and red fluorescence when associated with single-stranded DNA. An index of DNA denaturation per cell is provided by alpha-t [alpha t = red/(red   green) fluorescence]. The standard deviation (SD alpha t), coefficient of variation (CV alpha t) and proportion of cells outside the main population ([[COMP]] alpha t) of the alpha t distribution quantify the extent of denaturation for a sample. Intraclass correlations of the alpha t values were high (greater than or equal to 0.70), based on four collections obtained over several years from Group 1 bulls. Negative correlations were obtained between fertility ratings and both SD alpha t (-0.58, p less than 0.01) and [[COMP]] alpha t (-0.40, p less than 0.01) in Group 1, and between nonreturn rates and both SD alpha t (-0.65, p less than 0.01) and [[COMP]] alpha t (-0.53, p less than 0.05) in Group 2. These data suggest that the SCSA will be of value for identification of low fertility sires and poor quality semen samples.
|mesh-terms=* Aging
* Analysis of Variance
* Animals
* Cattle
* Cell Nucleus
* Chromatin
* Fertility
* Flow Cytometry
* Male
* Spermatozoa

|full-text-url=https://sci-hub.do/10.1095/biolreprod36.4.915
}}
{{medline-entry
|title=Effect of age and training on aerobic capacity and body composition of master athletes.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/3558232
|abstract=Maximum oxygen uptake (VO2max) and body composition have been shown to deteriorate with age. How much of the decline is attributable to aging and how much is affected by reduced physical activity is not known. The purpose of this investigation was to determine the aerobic capacity and body composition of 24 master track athletes and to evaluate the relationship to age and maintenance of training over a 10-yr period. The subjects (50-82 yr of age) were retested after a 10.1-yr follow-up (T2). All continued their aerobic training, but only 11 were still highly competitive ([[COMP]]) and continued to train at the same intensity. The other 13 athletes studied became noncompetitive (post-[[COMP]]) and reduced their training intensity. The results showed the [[COMP]] group to maintain its VO2max and maximum O2 pulse while the post-[[COMP]] group showed a significant decline (54.2-53.3 vs. 52.5-45.9 ml X kg-1 X min-1; 20.7-20.8 vs. 22.4-20.0 ml/beat from test one (T1) to T2 for the [[COMP]] vs. post-[[COMP]] groups, respectively). Maximum heart rate declined 7 beats/min for both groups. Body composition showed no difference between groups from T1 to T2. For both groups body weight declined slightly (70.0-68.9 kg), percent fat increased significantly (13.1-15.1%), and fat-free weight decreased significantly (61.0-59.0 kg). Thus, when training was maintained, aerobic capacity remained unchanged over the follow-up period. Body composition changed for both groups and may have been related to aging and/or the type of training performed.
|mesh-terms=* Aged
* Aged, 80 and over
* Aging
* Anthropometry
* Body Composition
* Heart Rate
* Hemodynamics
* Humans
* Male
* Middle Aged
* Oxygen Consumption
* Physical Education and Training
* Rest
* Spirometry
* Sports

|full-text-url=https://sci-hub.do/10.1152/jappl.1987.62.2.725
}}