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体干细胞中的JNK活性会导致衰老果蝇肠道组织稳态的丧失。

JNK activity in somatic stem cells causes loss of tissue homeostasis in the aging Drosophila gut.

作者信息

Biteau Benoît, Hochmuth Christine E, Jasper Heinrich

机构信息

Department of Biology, University of Rochester, River Campus Box 270211, Rochester, NY 14627, USA.

出版信息

Cell Stem Cell. 2008 Oct 9;3(4):442-55. doi: 10.1016/j.stem.2008.07.024.

Abstract

Metazoans employ cytoprotective and regenerative strategies to maintain tissue homeostasis. Understanding the coordination of these strategies is critical to developing accurate models for aging and associated diseases. Here we show that cytoprotective Jun N-terminal kinase (JNK) signaling influences regeneration in the Drosophila gut by directing proliferation of intestinal stem cells (ISCs). Interestingly, this function of JNK contributes to the loss of tissue homeostasis in old and stressed intestines by promoting the accumulation of misdifferentiated ISC daughter cells. Ectopic Delta/Notch signaling in these cells causes their abnormal differentiation but also limits JNK-induced proliferation. Protective JNK signaling and control of cell proliferation and differentiation by Delta/Notch signaling thus have to be carefully balanced to ensure tissue homeostasis. Our findings suggest that this balance is lost in old animals, increasing the potential for neoplastic transformation.

摘要

后生动物采用细胞保护和再生策略来维持组织稳态。了解这些策略的协调对于开发准确的衰老及相关疾病模型至关重要。在此我们表明,细胞保护型Jun氨基末端激酶(JNK)信号通过指导肠道干细胞(ISC)的增殖来影响果蝇肠道的再生。有趣的是,JNK的这一功能通过促进分化错误的ISC子代细胞的积累,导致衰老和应激肠道中组织稳态的丧失。这些细胞中异位的Delta/Notch信号会导致它们异常分化,但也会限制JNK诱导的增殖。因此,保护性JNK信号以及Delta/Notch信号对细胞增殖和分化的控制必须仔细平衡,以确保组织稳态。我们的研究结果表明,这种平衡在老年动物中丧失,增加了肿瘤转化的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46ac/3225008/ddcaba216002/nihms336757f1.jpg

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