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肠细胞中的辅助蛋白通过细胞间通讯控制肠道稳态。

Auxilin in enterocytes controls intestinal homeostasis through inter-cell communication.

作者信息

Wang Runqi, Li Zhengran, Wei Jing, Kong Ruiyan, Ren Xuejing, Zhao Hang, Zhang Danjie, Tao Liu Xiyue, Li Zhouhua

机构信息

Laboratory of Stem Cell Biology, College of Life Sciences, Capital Normal University, Beijing, China.

出版信息

Cell Death Dis. 2025 Aug 18;16(1):626. doi: 10.1038/s41419-025-07954-w.

Abstract

Residential stem cells sense extrinsic and intrinsic signals to proliferate accordingly to maintain homeostasis. However, how differentiated cells control stem cell proliferation still remains elusive. Here, we find that Auxilin (Aux) maintains enterocyte (EC) integrity to prevent unlimited intestinal stem cell (ISC) proliferation. Depleting aux in ECs leads to excessive ISC proliferation and intestinal homeostasis disruption. Ectopic cytokine production from dying aux-depleted ECs activates JAK/STAT signaling and promotes ISC proliferation. Mechanistically, Aux facilitates anterograde ER-to-Golgi apparatus (GA) vesicle transport by associating with COPII coatomer. Further, the presentation of cell adhesion molecules (CAMs) by ER-to-GA transport is required for intestinal homeostasis. Together, these data demonstrate that Aux maintains EC integrity by mediating ER-to-GA trafficking of CAMs to restrain excessive ISC proliferation. Thus our study uncovers the underlying mechanism of how differentiated cells control stem cell proliferation through inter-cell communication during tissue homeostasis and pathogenesis.

摘要

驻留干细胞感知外在和内在信号,相应地进行增殖以维持体内平衡。然而,分化细胞如何控制干细胞增殖仍然不清楚。在这里,我们发现辅助蛋白(Aux)维持肠上皮细胞(EC)的完整性,以防止肠道干细胞(ISC)无限增殖。在EC中耗尽Aux会导致ISC过度增殖和肠道内环境稳定破坏。垂死的耗尽Aux的EC异位产生细胞因子会激活JAK/STAT信号,并促进ISC增殖。从机制上讲,Aux通过与COPII包被蛋白结合促进从内质网(ER)到高尔基体(GA)的顺向囊泡运输。此外,ER到GA的运输所呈现的细胞粘附分子(CAM)是肠道内环境稳定所必需的。总之,这些数据表明Aux通过介导CAM从ER到GA的运输来维持EC的完整性,从而抑制ISC的过度增殖。因此,我们的研究揭示了在组织内环境稳定和发病机制过程中,分化细胞如何通过细胞间通讯控制干细胞增殖的潜在机制。

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