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Aging shifts mitochondrial dynamics toward fission to promote germline stem cell loss.
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- المؤلفون: Amartuvshin, Oyundari; Lin, Chi‐Hung; Hsu, Shao‐Chun; Kao, Shih‐Han; Chen, Alvin; Tang, Wei‐Chun; Chou, Han‐Lin; Chang, Dong‐Lin; Hsu, Yen‐Yang; Hsiao, Bai‐Shiou; Rastegari, Elham; Lin, Kun‐Yang; Wang, Yu‐Ting; Yao, Chi‐Kuang; Chen, Guang‐Chao; Chen, Bi‐Chang; Hsu, Hwei‐Jan
- المصدر:
Aging Cell; Aug2020, Vol. 19 Issue 8, p1-19, 19p
- الموضوع:
- معلومة اضافية
- نبذة مختصرة :
Changes in mitochondrial dynamics (fusion and fission) are known to occur during stem cell differentiation; however, the role of this phenomenon in tissue aging remains unclear. Here, we report that mitochondrial dynamics are shifted toward fission during aging of Drosophila ovarian germline stem cells (GSCs), and this shift contributes to aging‐related GSC loss. We found that as GSCs age, mitochondrial fragmentation and expression of the mitochondrial fission regulator, Dynamin‐related protein (Drp1), are both increased, while mitochondrial membrane potential is reduced. Moreover, preventing mitochondrial fusion in GSCs results in highly fragmented depolarized mitochondria, decreased BMP stemness signaling, impaired fatty acid metabolism, and GSC loss. Conversely, forcing mitochondrial elongation promotes GSC attachment to the niche. Importantly, maintenance of aging GSCs can be enhanced by suppressing Drp1 expression to prevent mitochondrial fission or treating with rapamycin, which is known to promote autophagy via TOR inhibition. Overall, our results show that mitochondrial dynamics are altered during physiological aging, affecting stem cell homeostasis via coordinated changes in stemness signaling, niche contact, and cellular metabolism. Such effects may also be highly relevant to other stem cell types and aging‐induced tissue degeneration. [ABSTRACT FROM AUTHOR]
- نبذة مختصرة :
Copyright of Aging Cell is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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