Редактирование: MRC1

Macrophage mannose receptor 1 precursor (MMR) (C-type lectin domain family 13 member D) (C-type lectin domain family 13 member D-like) (Human mannose receptor) (hMR) (Macrophage mannose receptor 1-like protein 1) (CD206 antigen) [CLEC13D] [CLEC13DL] [MRC1L1]

==Publications==

{{medline-entry
|title=Myocardial Infarction Superimposed on Aging: MMP-9 Deletion Promotes M2 Macrophage Polarization.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/25878031
|abstract=In this study, we examined the combined effect of aging and myocardial infarction on left ventricular remodeling, focusing on matrix metalloproteinase (MMP)-9-dependent mechanisms. We enrolled 55 C57BL/6J wild type (WT) and 85 MMP-9 Null (Null) mice of both sexes at 11-36 months of age and evaluated their response at Day 7 post-myocardial infarction. Plasma MMP-9 levels positively linked to age in WT mice (r = .46, p = .001). MMP-9 deletion improved survival (76% for WT vs 88% for Null, p = .021). Post-myocardial infarction, there was a progressive increase in left ventricular dilation with age in WT but not in Null mice. By inflammatory gene array analysis, WT mice showed linear age-dependent increases in three different proinflammatory genes (C3, CCl4, and CX3CL1; all p < .05), whereas Null mice showed increases in three proinflammatory genes (CCL5, CCL9, and CXCL4; all p < .05) and seven anti-inflammatory genes (CCL1, CCL6, [[CCR1]], [[IL11]], IL1r2, IL8rb, and Mif; all p < .05). Compared with WT, macrophages isolated from Null left ventricle infarct demonstrated enhanced expression of anti-inflammatory M2 markers [[CD163]], [[MRC1]], TGF-β1, and YM1 (all p < .05), without affecting proinflammatory M1 markers. In conclusion, MMP-9 deletion stimulated anti-inflammatory polarization of macrophages to attenuate left ventricle dysfunction in the aging post-myocardial infarction. 
|mesh-terms=* Aging
* Animals
* Cytokines
* Echocardiography
* Female
* Gene Expression
* Immunohistochemistry
* Ligation
* Male
* Matrix Metalloproteinase 9
* Mice
* Mice, Inbred C57BL
* Myocardial Infarction
* Real-Time Polymerase Chain Reaction
* Survival Analysis
* Ventricular Remodeling
|keywords=* Aging
* Cardiac remodeling
* M2 phenotype.
* Macrophage polarization
|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5175450
}}