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Hippo signaling regulates Drosophila intestine stem cell proliferation through multiple pathways

机译:河马信号通过多种途径调节果蝇肠道干细胞的增殖

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摘要

Intestinal stem cells (ISCs) in the Drosophila adult midgut are essential for maintaining tissue homeostasis and replenishing lost cells in response to tissue damage. Here we demonstrate that the Hippo (Hpo) signaling pathway, an evolutionarily conserved pathway implicated in organ size control and tumorigenesis, plays an essential role in regulating ISC proliferation. Loss of Hpo signaling in either midgut precursor cells or epithelial cells stimulates ISC proliferation. We provide evidence that loss of Hpo signaling in epithelial cells increases the production of cytokines of the Upd family and multiple EGFR ligands that activate JAK-STAT and EGFR signaling pathways in ISCs to stimulate their proliferation, thus revealing a unique non–cell-autonomous role of Hpo signaling in blocking ISC proliferation. Finally, we show that the Hpo pathway mediator Yorkie (Yki) is also required in precursor cells for injury-induced ISC proliferation in response to tissue-damaging reagent DSS.
机译:果蝇成年中肠中的肠道干细胞(ISC)对于维持组织动态平衡和补充对组织损伤的损失细胞至关重要。在这里,我们证明了河马(Hpo)信号传导途径,一种涉及器官大小控制和肿瘤发生的进化保守途径,在调节ISC增殖中起着至关重要的作用。中肠前体细胞或上皮细胞中Hpo信号的丢失会刺激ISC增殖。我们提供的证据表明,上皮细胞中Hpo信号的缺失增加了Upd家族和多种EGFR配体的细胞因子的产生,这些配体激活了ISC中的JAK-STAT和EGFR信号通路,从而刺激了它们的增殖,从而揭示了独特的非细胞自主作用Hpo信号传导在阻断ISC增殖中的作用。最后,我们显示Hpo途径介导的约克(Yki)在前体细胞中还需要用于损伤诱导的ISC增殖,以响应组织破坏剂DSS。

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