1. Department of Biomedical Engineering, Center for Ultrafast Optical Science
2. Life Sciences Institute, Center for Stem Cell Biology,
3. Department of Cell and Developmental Biology, University of Michigan, Ann Arbor, Michigan 48109, USA
4. Departments of Developmental Biology and Genetics, Stanford University, School of Medicine, Stanford, California 94305, USA
5. These authors contributed equally to this work.
6. Present address: Peter MacCallum Cancer Centre, Anatomy and Cell Biology Department, University of Melbourne, Melbourne, Victoria 3002, Australia.

Correspondence to: Yukiko M. Yamashita^2,3 Correspondence and requests for materials should be addressed to Y.M.Y. (Email: yukikomy@umich.edu).

Abstract

Asymmetric division of adult stem cells generates one self-renewing stem cell and one differentiating cell, thereby maintaining tissue homeostasis. A decline in stem cell function has been proposed to contribute to tissue ageing, although the underlying mechanism is poorly understood. Here we show that changes in the stem cell orientation with respect to the niche during ageing contribute to the decline in spermatogenesis in the male germ line of Drosophila. Throughout the cell cycle, centrosomes in germline stem cells (GSCs) are oriented within their niche and this ensures asymmetric division. We found that GSCs containing misoriented centrosomes accumulate with age and that these GSCs are arrested or delayed in the cell cycle. The cell cycle arrest is transient, and GSCs appear to re-enter the cell cycle on correction of centrosome orientation. On the basis of these findings, we propose that cell cycle arrest associated with centrosome misorientation functions as a mechanism to ensure asymmetric stem cell division, and that the inability of stem cells to maintain correct orientation during ageing contributes to the decline in spermatogenesis. We also show that some of the misoriented GSCs probably originate from dedifferentiation of spermatogonia.

1. Department of Biomedical Engineering, Center for Ultrafast Optical Science
2. Life Sciences Institute, Center for Stem Cell Biology,
3. Department of Cell and Developmental Biology, University of Michigan, Ann Arbor, Michigan 48109, USA
4. Departments of Developmental Biology and Genetics, Stanford University, School of Medicine, Stanford, California 94305, USA
5. These authors contributed equally to this work.
6. Present address: Peter MacCallum Cancer Centre, Anatomy and Cell Biology Department, University of Melbourne, Melbourne, Victoria 3002, Australia.

Correspondence to: Yukiko M. Yamashita^2,3 Correspondence and requests for materials should be addressed to Y.M.Y. (Email: yukikomy@umich.edu).

MORE ARTICLES LIKE THIS

These links to content published by NPG are automatically generated.