肠道巨噬细胞的组织特异性分化需要 TGFβ 受体介导的信号转导。

Tissue-specific differentiation of colonic macrophages requires TGFβ receptor-mediated signaling.

机构信息

Centre for Immunobiology, Institute of Infection, Immunity and Inflammation, College of Medicine, Veterinary Medicine and Life Sciences, University of Glasgow, Scotland, UK.

Institute of Immunology, Hannover Medical School, Hannover, Germany.

出版信息

Mucosal Immunol. 2017 Nov;10(6):1387-1399. doi: 10.1038/mi.2016.142. Epub 2017 Feb 1.

Abstract

Intestinal macrophages (mφ) form one of the largest populations of mφ in the body and are vital for the maintenance of gut homeostasis. They have several unique properties and are derived from local differentiation of classical Ly6C monocytes, but the factors driving this tissue-specific process are not understood. Here we have used global transcriptomic analysis to identify a unique homeostatic signature of mature colonic mφ that is acquired as they differentiate in the mucosa. By comparing the analogous monocyte differentiation process found in the dermis, we identify TGFβ as an indispensable part of monocyte differentiation in the intestine and show that it enables mφ to adapt precisely to the requirements of their environment. Importantly, TGFβR signaling on mφ has a crucial role in regulating the accumulation of monocytes in the mucosa, via mechanisms that are distinct from those used by IL10.

摘要

肠道巨噬细胞(mφ)是体内最大的巨噬细胞群体之一,对于维持肠道内环境稳态至关重要。它们具有几个独特的特性,来源于经典 Ly6C 单核细胞的局部分化,但驱动这种组织特异性过程的因素尚不清楚。在这里,我们使用全转录组分析鉴定了成熟结肠 mφ 的独特稳态特征,这些特征是在其分化为黏膜细胞时获得的。通过比较在真皮中发现的类似单核细胞分化过程,我们发现 TGFβ 是肠道中单核细胞分化不可或缺的一部分,并表明它使 mφ 能够精确地适应其环境的要求。重要的是,mφ 上的 TGFβR 信号在调节单核细胞在黏膜中的积累方面发挥着关键作用,其机制与 IL10 不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48bc/5417360/1bdfd234b0c5/emss-70945-f001.jpg

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