Редактирование: NFATC1 (раздел)

==Publications==

{{medline-entry
|title=Age-dependent human β cell proliferation induced by glucagon-like peptide 1 and calcineurin signaling.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/28920919
|abstract=Inadequate pancreatic β cell function underlies type 1 and type 2 diabetes mellitus. Strategies to expand functional cells have focused on discovering and controlling mechanisms that limit the proliferation of human β cells. Here, we developed an engraftment strategy to examine age-associated human islet cell replication competence and reveal mechanisms underlying age-dependent decline of β cell proliferation in human islets. We found that exendin-4 (Ex-4), an agonist of the glucagon-like peptide 1 receptor (GLP-1R), stimulates human β cell proliferation in juvenile but not adult islets. This age-dependent responsiveness does not reflect loss of GLP-1R signaling in adult islets, since Ex-4 treatment stimulated insulin secretion by both juvenile and adult human β cells. We show that the mitogenic effect of Ex-4 requires calcineurin/nuclear factor of activated T cells (NFAT) signaling. In juvenile islets, Ex-4 induced expression of calcineurin/NFAT signaling components as well as target genes for proliferation-promoting factors, including [[NFATC1]], [[FOXM1]], and [[CCNA1]]. By contrast, expression of these factors in adult islet β cells was not affected by Ex-4 exposure. These studies reveal age-dependent signaling mechanisms regulating human β cell proliferation, and identify elements that could be adapted for therapeutic expansion of human β cells.
|mesh-terms=* Adult
* Aging
* Animals
* Calcineurin
* Cyclin A1
* Exenatide
* Female
* Forkhead Box Protein M1
* Glucagon-Like Peptide 1
* Glucagon-Like Peptide-1 Receptor
* Humans
* Insulin
* Insulin Secretion
* Insulin-Secreting Cells
* Male
* Mice, Inbred NOD
* Middle Aged
* NFATC Transcription Factors
* Peptides
* Signal Transduction
* Venoms

|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617654
}}
{{medline-entry
|title=Genome-wide methylation analysis reveals differentially methylated loci that are associated with an age-dependent increase in bovine fibroblast response to LPS.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/28545453
|abstract=Differences in DNA methylation are known to contribute to the development of immune-related disorders in humans but relatively little is known about how methylation regulates immune function in cattle. Utilizing whole-transcriptome analyses of bovine dermal fibroblasts, we have previously identified an age and breed-dependent up-regulation of genes within the toll-like receptor 4 (TLR4) pathway that correlates with enhanced fibroblast production of IL-8 in response to lipopolysaccharide (LPS). Age-dependent differences in IL-8 production are abolished by treatment with 5-aza-2-deoxycytidine and Trichostatin A (AZA-TSA), suggesting epigenetic regulation of the innate response to LPS. In the current study, we performed reduced representation bisulfite sequencing (RRBS) on fibroblast cultures isolated from the same animals at 5- and 16-months of age to identify genes that exhibit variable methylation with age. To validate the role of methylation in gene expression, six innate response genes that were hyper-methylated in young animals were assessed by RT-qPCR in fibroblasts from animals at different ages and from different breeds. We identified 14,094 differentially methylated CpGs (DMCs) that differed between fibroblast cultures at 5- versus 16-months of age. Of the 5065 DMCs that fell within gene regions, 1117 were located within promoters, 1057 were within gene exons and 2891 were within gene introns and 67% were more methylated in young cultures. Transcription factor enrichment of the promoter regions hyper-methylated in young cultures revealed significant regulation by the key pro-inflammatory regulator, NF-κB. Additionally, five out of six chosen genes (PIK3R1, [[FES]], [[NFATC1]], [[TNFSF13]] and RORA) that were more methylated in young cultures showed a significant reduction in expression post-LPS treatment in comparison with older cultures. Two of these genes, [[FES]] and [[NFATC1]], were similarly down-regulated in Angus cultures that also exhibit a low LPS response phenotype. Our study has identified immune-related loci regulated by DNA methylation in cattle that may contribute to differential cellular response to LPS, two of which exhibit an identical expression profile in both low-responding age and breed phenotypes. Methylation biomarkers of differential immunity may prove useful in developing selection strategies for replacement cows that are less susceptible to severe infections, such as coliform mastitis.
|mesh-terms=* Aging
* Animals
* Cattle
* DNA Methylation
* Epigenesis, Genetic
* Fibroblasts
* Genetic Loci
* Genomics
* Interleukin-6
* Interleukin-8
* Lipopolysaccharides
* Transcriptome
|keywords=* DNA Methylation
* Inflammation
* Innate Immunity
* LPS
* RRBS
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445414
}}