Integrin αEβ7+ T cells direct intestinal stem cell fate decisions via adhesion signaling

整合素αEβ7+ T细胞通过黏附信号传导指导肠道干细胞命运决定

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作者:Shiyang Chen # ,Yajuan Zheng # ,Xiaojuan Ran # ,Hui Du ,Hua Feng ,Lei Yang ,Yating Wen ,Changdong Lin ,Shihui Wang ,Mengwen Huang ,Zhanjun Yan ,Dianqing Wu ,Hongyan Wang ,Gaoxiang Ge ,An Zeng ,Yi Arial Zeng ,Jianfeng Chen

Abstract

Intestinal stem cell (ISC) differentiation is regulated precisely by a niche in the crypt, where lymphocytes may interact with stem and transient amplifying (TA) cells. However, whether and how lymphocyte-stem/TA cell contact affects ISC differentiation is largely unknown. Here, we uncover a novel role of T cell-stem/TA cell contact in ISC fate decisions. We show that intestinal lymphocyte depletion results in skewed ISC differentiation in mice, which can be rescued by T cell transfer. Mechanistically, integrin αEβ7 expressed on T cells binds to E-cadherin on ISCs and TA cells, triggering E-cadherin endocytosis and the consequent Wnt and Notch signaling alterations. Blocking αEβ7-E-cadherin adhesion suppresses Wnt signaling and promotes Notch signaling in ISCs and TA cells, leading to defective ISC differentiation. Thus, αEβ7+ T cells regulate ISC differentiation at single-cell level through cell-cell contact-mediated αEβ7-E-cadherin adhesion signaling, highlighting a critical role of the T cell-stem/TA cell contact in maintaining intestinal homeostasis.

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