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Smad-Independent BMP Signaling in Somatic Cells Limits the Size of the Germline Stem Cell Pool
Author(s) -
ChenYuan Tseng,
YuHan Su,
ShunMin Yang,
KunYang Lin,
Chun-Ming Lai,
Elham Rastegari,
Oyundari Amartuvshin,
Yueh Cho,
Yu Cai,
HweiJan Hsu
Publication year - 2018
Publication title -
stem cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.207
H-Index - 76
ISSN - 2213-6711
DOI - 10.1016/j.stemcr.2018.07.008
Subject(s) - biology , microbiology and biotechnology , stem cell , germline , somatic cell , bone morphogenetic protein , smad , signal transduction , niche , soma , genetics , gene , neuroscience , ecology
In developing organisms, proper tuning of the number of stem cells within a niche is critical for the maintenance of adult tissues; however, the involved mechanisms remain largely unclear. Here, we demonstrate that Thickveins (Tkv), a type I bone morphogenetic protein (BMP) receptor, acts in the Drosophila developing ovarian soma through a Smad-independent pathway to shape the distribution of BMP signal within the niche, impacting germline stem cell (GSC) recruitment and maintenance. Somatic Tkv promotes Egfr signaling to silence transcription of Dally, which localizes BMP signals on the cell surface. In parallel, Tkv promotes Hh signaling, which promotes escort cell cellular protrusions and upregulates expression of the Drosophila BMP homolog, Dpp, forming a positive feedback loop that enhances Tkv signaling and strengthens the niche boundary. Our results reveal a role for non-canonical BMP signaling in the soma during GSC establishment and generally illustrate how complex, cell-specific BMP signaling mediates niche-stem cell interactions.

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