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乳粘连蛋白直系同源物抑制人、猪和鼠肠道上皮细胞的迁移。

Lactadherin orthologs inhibit migration of human, porcine and murine intestinal epithelial cells.

作者信息

Nyegaard Steffen, Andreasen Trine, Rasmussen Jan Trige

机构信息

Department of Molecular Biology University of Aarhus Aarhus C Denmark.

出版信息

Food Sci Nutr. 2017 May 15;5(4):934-942. doi: 10.1002/fsn3.479. eCollection 2017 Jul.

Abstract

Lactadherin was originally described due to its appearance in milk, but is abundantly expressed especially by professional and nonprofessional phagocytes. The proteins has been shown to have a multitude of bioactive effects, including inhibition of inflammatory phospholipases, induction of effero- and phagocytosis, prevent rotavirus induced gastroenteritis, and modulate intestinal homeostasis by regulating epithelial cell migration. The level of expression seems to be important in a row of serious pathologies linked to the intestinal epithelial barrier function, vascular- and autoimmune disease. This study examines the ability of lactadherin to modulate migration of intestinal epithelium. A cell exclusion assay is used to quantify the ability of human, bovine and murine lactadherin orthologs to affect migration of primary small intestine epithelium cells. Previous reports show that recombinant murine lactadherin stimulate rat small intestine cell migration. The present study could not confirm this. Conversely, 10 μg/ml lactadherin inhibits migration. Therefore, as lactadherins enteroprotective properties is well established using in vivo models we conclude that the protective effects are linked to lactadherins ability operate as an opsonin, or other modulating effects, and not a direct lactadherin-cell induction of migration. Thus, the molecular mechanism behind the enteroprotective role of lactadherin remains to be established.

摘要

乳黏附素最初因其在乳汁中的出现而被描述,但在专业和非专业吞噬细胞中大量表达。该蛋白已被证明具有多种生物活性作用,包括抑制炎性磷脂酶、诱导胞葬作用和吞噬作用、预防轮状病毒引起的肠胃炎以及通过调节上皮细胞迁移来调节肠道内环境稳定。在一系列与肠道上皮屏障功能、血管和自身免疫性疾病相关的严重病理状况中,其表达水平似乎很重要。本研究考察了乳黏附素调节肠道上皮细胞迁移的能力。采用细胞排斥试验来量化人、牛和鼠乳黏附素直系同源物影响原代小肠上皮细胞迁移的能力。先前的报道表明重组鼠乳黏附素能刺激大鼠小肠细胞迁移。本研究未能证实这一点。相反,10μg/ml的乳黏附素会抑制迁移。因此,鉴于乳黏附素的肠道保护特性在体内模型中已得到充分证实,我们得出结论,其保护作用与乳黏附素作为调理素发挥作用的能力或其他调节作用有关,而非乳黏附素对细胞迁移的直接诱导作用。因此,乳黏附素肠道保护作用背后的分子机制仍有待确定。

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