scholarly journals Decline in Self-Renewal Factors Contributes to Aging of the Stem Cell Niche in the Drosophila Testis

2007 ◽  
Vol 1 (4) ◽  
pp. 470-478 ◽  
Author(s):  
Monica Boyle ◽  
Chihunt Wong ◽  
Michael Rocha ◽  
D. Leanne Jones
2021 ◽  
Vol 402 (1) ◽  
pp. 112511
Author(s):  
Min Wang ◽  
Xiaojin Luan ◽  
Yidan Yan ◽  
Qianwen Zheng ◽  
Wanyin Chen ◽  
...  

Aging ◽  
2019 ◽  
Vol 11 (3) ◽  
pp. 855-873
Author(s):  
Perinthottathil Sreejith ◽  
Wijeong Jang ◽  
Van To ◽  
Yong Hun Jo ◽  
Benoit Biteau ◽  
...  

2014 ◽  
Vol 10 (12) ◽  
pp. e1004577 ◽  
Author(s):  
Michelle E. Toomey ◽  
Horacio M. Frydman

Nature ◽  
2008 ◽  
Vol 454 (7208) ◽  
pp. 1132-1136 ◽  
Author(s):  
Justin Voog ◽  
Cecilia D’Alterio ◽  
D. Leanne Jones

eLife ◽  
2014 ◽  
Vol 3 ◽  
Author(s):  
Aiguo Tian ◽  
Jin Jiang

Stem cells are maintained in a specialized microenvironment called niche but the nature of stem cell niche remains poorly defined in many systems. Here we demonstrate that intestinal epithelium-derived BMP serves as a niche signal for intestinal stem cell (ISC) self-renewal in Drosophila adult midgut. We find that BMP signaling is asymmetric between ISC and its differentiated daughter cell. Two BMP ligands, Dpp and Gbb, are produced by enterocytes and act in conjunction to promote ISC self-renewal by antagonizing Notch signaling. Furthermore, the basement membrane-associated type IV collagens regulate ISC self-renewal by confining higher BMP signaling to ISCs. The employment of gut epithelia as a niche for stem cell self-renewal may provide a mechanism for direct communication between the niche and the environment, allowing niche signal production and stem cell number to be fine-tuned in response to various physiological and pathological stimuli.


2006 ◽  
Vol 290 (2) ◽  
pp. G189-G193 ◽  
Author(s):  
Neil D. Theise

This essay will address areas of liver stem/progenitor cell studies in which consensus has emerged and in which controversy still prevails over consensus, but it will also highlight important themes that inevitably should be a focus of liver stem/progenitor cell investigations in coming years. Thus concepts regarding cell plasticity, the existence of a physiological/anatomic stem cell niche, and whether intrahepatic liver stem/progenitor cells comprise true stem cells or progenitor cells (or both) will be approached in some detail.


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