跳到正文
PLOS Genetics· Runqi Wang·· 8 小时前AI 评分38

果蝇肠内分泌细胞中的 Auxilin 通过细胞间信号传递调控肠道稳态

Auxilin in enteroendocrine cells controls intestinal homeostasis through inter-cell signaling relays

AI 导读

果蝇肠内分泌细胞(EEs)中的 Auxilin(Aux)通过限制肠道干细胞(ISC)增殖维持肠道稳态。在全部 EEs 中敲低 aux 会破坏肠道稳态;aux 缺失的 EEs 中 Slit 水平显著下降,部分 aux 缺失 EEs 及邻近野生型肠细胞中细胞因子 Upd3 表达显著升高。在 pros ts > aux RNAi 肠道中异位表达 slit 可有效挽救缺陷;aux 缺失 EEs 中 EGFR 积累导致 EGFR 信号异位激活,进一步抑制 EGFR 信号可完全抑制该肠道缺陷。

阅读原文

来源:PLOS Genetics · journals.plos.org

论文摘要

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

Adult stem cells are critical for the homeostasis of residential tissue and organism fitness. Residential stem cells must constantly perceive external and internal signals and adjust their proliferation rate accordingly to avoid unlimited proliferation or premature differentiation. However, how differentiated cells affect stem cell proliferation and tissue homeostasis through cell-cell communication still remains poorly understood. Here, we unveil an unprecedented function of Auxilin (Aux) in enteroendocrine cells (EEs) by restricting intestinal stem cell (ISC) proliferation. aux depletion in all EEs leads to intestinal homeostasis disruption. The levels of Slit are dramatically reduced in aux-depleted EEs and cytokine Upd3 expression is significantly increased in some aux-depleted EEs and neighboring wild type enterocytes (ECs). Ectopic expression of slit could effectively rescue the defects observed in prosts > auxRNAi intestines. Interestingly, EGFR signaling is ectopically activated due to EGFR accumulation in aux-depleted EEs. Further inhibiting EGFR signaling completely suppresses the defects in prosts > auxRNAi intestines. Finally, EGFR signaling suppresses slit transcription by Pointed binding to slit regulatory regions. Together, these data show that Aux in EEs restrains ISCs from excessive proliferation and aberrant progeny differentiation to maintain intestinal homeostasis through inter-cell communications. Thus our study uncovers the underlying mechanism of how stem cell proliferation is properly controlled by differentiated cells through inter-cell signaling relays during tissue homeostasis and tumorigenesis.