极性(国际关系)
基础(医学)
细胞生物学
干细胞
生物
电池极性
细胞
遗传学
内分泌学
胰岛素
作者
Song Wu,Yang Yang,Ruizhi Tang,Song Zhang,Peizhong Qin,Rong Lin,Neus Rafel,Elena M. Lucchetta,Benjamin Ohlstein,Zheng Guo
出处
期刊:Cell Reports
[Elsevier]
日期:2023-02-01
卷期号:42 (2): 112093-112093
被引量:13
标识
DOI:10.1016/j.celrep.2023.112093
摘要
Apical-basal polarity and cell-fate determinants are crucial for the cell fate and control of stem cell numbers. However, their interplay leading to a precise stem cell number remains unclear. Drosophila pupal intestinal stem cells (pISCs) asymmetrically divide, generating one apical ISC progenitor and one basal Prospero (Pros)+ enteroendocrine mother cell (EMC), followed by symmetric divisions of each daughter before adulthood, providing an ideal system to investigate the outcomes of polarity loss. Using lineage tracing and ex vivo live imaging, we identify an interlocked polarity regulation network precisely determining ISC number: Bazooka inhibits Pros accumulation by activating Notch signaling to maintain stem cell fate in pISC apical daughters. A threshold of Pros promotes differentiation to EMCs and avoids ISC-like cell fate, and over-threshold of Pros inhibits miranda expression to ensure symmetric divisions in pISC basal daughters. Our work suggests that a polarity-dependent threshold of a differentiation factor precisely controls stem cell number.
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