4.7 Article

Metalloendopeptidase ADAM-like Decysin 1 (ADAMDEC1) in Colonic Subepithelial PDGFRα+ Cells Is a New Marker for Inflammatory Bowel Disease

期刊

出版社

MDPI
DOI: 10.3390/ijms23095007

关键词

ADAMDEC1; mucosal PDGFR alpha(+) cells; inflammatory bowel disease; Crohn's disease; DSS colitis

资金

  1. National Institute of Diabetes and Digestive and Kidney Diseases [R01DK094886, R01DK103055, R01DK091336, P01DK41315]

向作者/读者索取更多资源

ADAMDEC1 is selectively expressed in PDGFR alpha(+) cells in the colonic mucosa and may serve as a diagnostic and therapeutic target for intestinal inflammation and Crohn's disease.
Metalloendopeptidase ADAM-Like Decysin 1 (ADAMDEC1) is an anti-inflammatory peptidase that is almost exclusively expressed in the gastrointestinal (GI) tract. We have recently found abundant and selective expression of Adamdec1 in colonic mucosal PDGFR alpha(+) cells. However, the cellular origin for this gene expression is controversial as it is also known to be expressed in intestinal macrophages. We found that Adamdec1 mRNAs were selectively expressed in colonic mucosal subepithelial PDGFR alpha(+) cells. ADAMDEC1 protein was mainly released from PDGFR alpha(+) cells and accumulated in the mucosal layer lamina propria space near the epithelial basement membrane. PDGFR alpha(+) cells significantly overexpressed Adamdec1 mRNAs and protein in DSS-induced colitis mice. Adamdec1 was predominantly expressed in CD45(-) PDGFR alpha(+) cells in DSS-induced colitis mice, with only minimal expression in CD45(+) CD64(+) macrophages. Additionally, overexpression of both ADAMDEC1 mRNA and protein was consistently observed in PDGFR alpha(+) cells, but not in CD64(+) macrophages found in human colonic mucosal tissue affected by Crohn's disease. In summary, PDGFR alpha(+) cells selectively express ADAMDEC1, which is localized to the colon mucosa layer. ADAMDEC1 expression significantly increases in DSS-induced colitis affected mice and Crohn's disease affected human tissue, suggesting that this gene can serve as a diagnostic and/or therapeutic target for intestinal inflammation and Crohn's disease.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据