Intestinal stem cell response to injury: lessons from Drosophila

被引:103
作者
Jiang, Huaqi [1 ]
Tian, Aiguo [1 ]
Jiang, Jin [1 ,2 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
[2] Univ Texas Southwestern Med Ctr Dallas, Dept Pharmacol, Dallas, TX 75390 USA
关键词
ISC; midgut; Wnt; Wg; Hedgehog; Hh; BMP; Dpp; Gbb; EGFR; Ras; Hippo; Yki; Yap; JAK-STAT; JNK; Notch; N; Insulin; InR; Calcium; microRNA; Aging; Tissue damage; Self-renewal; Symmetric division; Asymmetric division; Proliferation; Regeneration; Tumor; HIPPO SIGNALING PATHWAY; ADULT MIDGUT REGENERATION; ENTEROENDOCRINE CELLS; TRANSCRIPTION FACTOR; BACTERIAL-INFECTION; JUVENILE POLYPOSIS; TISSUE HOMEOSTASIS; MULTIPLE PATHWAYS; POSTERIOR MIDGUT; SELF-RENEWAL;
D O I
10.1007/s00018-016-2235-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Many adult tissues and organs are maintained by resident stem cells that are activated in response to injury but the mechanisms that regulate stem cell activity during regeneration are still poorly understood. An emerging system to study such problem is the Drosophila adult midgut. Recent studies have identified both intrinsic factors and extrinsic niche signals that control the proliferation, self-renewal, and lineage differentiation of Drosophila adult intestinal stem cells (ISCs). These findings set up the stage to interrogate how niche signals are regulated and how they are integrated with cell-intrinsic factors to control ISC activity during normal homeostasis and regeneration. Here we review the current understanding of the mechanisms that control ISC self-renewal, proliferation, and lineage differentiation in Drosophila adult midgut with a focus on the niche signaling network that governs ISC activity in response to injury.
引用
收藏
页码:3337 / 3349
页数:13
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