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Cytokine/Jak/Stat Signaling Mediates Regeneration and Homeostasis in the Drosophila Midgut

机译:细胞因子/ Jak / Stat信号介导果蝇中肠的再生和体内稳态。

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摘要

Cells in intestinal epithelia turn over rapidly due to damage from digestion and toxins produced by the enteric microbiota. Gut homeostasis is maintained by intestinal stem cells (ISCs) that divide to replenish the intestinal epithelium, but little is known about how ISC division and differentiation are coordinated with epithelial cell loss. We show here that when enterocytes (ECs) in the Drosophila midgut are subjected to apoptosis, enteric infection, or JNK-mediated stress signaling, they produce cytokines (Upd, Upd2, and Upd3) that activate Jak/Stat signaling in ISCs, promoting their rapid division. Upd/Jak/Stat activity also promotes progenitor cell differentiation, in part by stimulating Delta/Notch signaling, and is required for differentiation in both normal and regenerating midguts. Hence, cytokine-mediated feedback enables stem cells to replace spent progeny as they are lost, thereby establishing gut homeostasis.
机译:肠上皮细胞由于肠微生物群产生的消化和毒素破坏而迅速翻转。肠道的稳态是由肠道干细胞(ISC)维持的,该干细胞分裂以补充肠道上皮,但是对ISC的分裂和分化与上皮细胞丢失的协调关系知之甚少。我们在这里显示,当果蝇中肠中的肠上皮细胞(ECs)受到凋亡,肠感染或JNK介导的应激信号转导时,它们会产生激活ISC中Jak / Stat信号转导的细胞因子(Upd,Upd2和Upd3),从而促进它们快速分裂。 Upd / Jak / Stat活性还通过部分刺激Delta / Notch信号来促进祖细胞分化,并且是正常和再生中肠分化所必需的。因此,细胞因子介导的反馈使干细胞能够在失去后代后代后代,从而建立肠道稳态。

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