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    0

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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