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分泌型基质蛋白 ISLR 通过抑制上皮 Hippo 信号通路促进肠道再生。

Secreted stromal protein ISLR promotes intestinal regeneration by suppressing epithelial Hippo signaling.

机构信息

State Key Laboratories for Agrobiotechnology and Beijing Advanced Innovation Center for Food Nutrition and Human Health, College of Biological Sciences, China Agricultural University, Beijing, China.

Guangdong Provincial Key Laboratory of Regional Immunity and School of Medicine, Shenzhen University, Shenzhen, China.

出版信息

EMBO J. 2020 Apr 1;39(7):e103255. doi: 10.15252/embj.2019103255. Epub 2020 Mar 4.

Abstract

The Hippo-YAP signaling pathway plays an essential role in epithelial cells during intestinal regeneration and tumorigenesis. However, the molecular mechanism linking stromal signals to YAP-mediated intestinal regeneration and tumorigenesis is poorly defined. Here, we report a stroma-epithelium ISLR-YAP signaling axis essential for stromal cells to modulate epithelial cell growth during intestinal regeneration and tumorigenesis. Specifically, upon inflammation and in cancer, an oncogenic transcription factor ETS1 in stromal cells induces expression of a secreted protein ISLR that can inhibit Hippo signaling and activate YAP in epithelial cells. Deletion of Islr in stromal cells in mice markedly impaired intestinal regeneration and suppressed tumorigenesis in the colon. Moreover, the expression of stromal cell-specific ISLR and ETS1 significantly increased in inflamed mucosa of human IBD patients and in human colorectal adenocarcinoma, accounting for the epithelial YAP hyperactivation. Collectively, our findings provide new insights into the signaling crosstalk between stroma and epithelium during tissue regeneration and tumorigenesis.

摘要

Hippo-YAP 信号通路在肠道再生和肿瘤发生过程中对上皮细胞起着至关重要的作用。然而,将基质信号与 YAP 介导的肠道再生和肿瘤发生联系起来的分子机制还不清楚。在这里,我们报告了一个间质-上皮 ISLR-YAP 信号轴,它对于基质细胞在肠道再生和肿瘤发生过程中调节上皮细胞生长是必需的。具体来说,在炎症和癌症中,基质细胞中的致癌转录因子 ETS1 诱导一种分泌蛋白 ISLR 的表达,该蛋白可抑制 Hippo 信号通路并激活上皮细胞中的 YAP。在小鼠中,基质细胞中 Islr 的缺失显著损害了肠道再生,并抑制了结肠中的肿瘤发生。此外,在人类 IBD 患者的炎症黏膜和人类结直肠腺癌中,基质细胞特异性 ISLR 和 ETS1 的表达显著增加,这解释了上皮细胞 YAP 的过度激活。总之,我们的研究结果为组织再生和肿瘤发生过程中基质和上皮之间的信号串扰提供了新的见解。

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