TY - JOUR
T1 - Wnt signaling-mediated redox regulation maintains the germ line stem cell differentiation niche
AU - Wang, Su
AU - Gao, Yuan
AU - Song, Xiaoqing
AU - Ma, Xing
AU - Zhu, Xiujuan
AU - Mao, Ying
AU - Yang, Zhihao
AU - Ni, Jianquan
AU - Li, Hua
AU - Malanowski, Kathryn E.
AU - Anoj, Perera
AU - Park, Jungeun
AU - Haug, Jeff
AU - Xie, Ting
N1 - Publisher Copyright:
© Wang et al.
PY - 2015/10/9
Y1 - 2015/10/9
N2 - Adult stem cells continuously undergo self-renewal and generate differentiated cells. In the Drosophila ovary, two separate niches control germ line stem cell (GSC) self-renewal and differentiation processes. Compared to the self-renewing niche, relatively little is known about the maintenance and function of the differentiation niche. In this study, we show that the cellular redox state regulated by Wnt signaling is critical for the maintenance and function of the differentiation niche to promote GSC progeny differentiation. Defective Wnt signaling causes the loss of the differentiation niche and the upregulated BMP signaling in differentiated GSC progeny, thereby disrupting germ cell differentiation. Mechanistically, Wnt signaling controls the expression of multiple glutathione-S-transferase family genes and the cellular redox state. Finally, Wnt2 and Wnt4 function redundantly to maintain active Wnt signaling in the differentiation niche. Therefore, this study has revealed a novel strategy for Wnt signaling in regulating the cellular redox state and maintaining the differentiation niche.
AB - Adult stem cells continuously undergo self-renewal and generate differentiated cells. In the Drosophila ovary, two separate niches control germ line stem cell (GSC) self-renewal and differentiation processes. Compared to the self-renewing niche, relatively little is known about the maintenance and function of the differentiation niche. In this study, we show that the cellular redox state regulated by Wnt signaling is critical for the maintenance and function of the differentiation niche to promote GSC progeny differentiation. Defective Wnt signaling causes the loss of the differentiation niche and the upregulated BMP signaling in differentiated GSC progeny, thereby disrupting germ cell differentiation. Mechanistically, Wnt signaling controls the expression of multiple glutathione-S-transferase family genes and the cellular redox state. Finally, Wnt2 and Wnt4 function redundantly to maintain active Wnt signaling in the differentiation niche. Therefore, this study has revealed a novel strategy for Wnt signaling in regulating the cellular redox state and maintaining the differentiation niche.
UR - https://www.webofscience.com/wos/woscc/full-record/WOS:000362840300001
UR - https://openalex.org/W2217269418
UR - https://www.scopus.com/pages/publications/84946600679
U2 - 10.7554/eLife.08174
DO - 10.7554/eLife.08174
M3 - Journal Article
C2 - 26452202
SN - 2050-084X
VL - 4
JO - eLife
JF - eLife
IS - OCTOBER2015
M1 - e08174
ER -