Stem cells resume asymmetric division upon niche re-entry through reactivating the centrosome orientation checkpoint

In Drosophila testis, germline stem cells (GSCs) typically divide asymmetrically, keeping one daughter cell within the niche for self-renewal and placing the other daughter cell outside the niche to undergo differentiation. This is the primary mechanism for maintaining a stable number of stem cells in the niche. However, it has been shown that small fraction of GSCs continuously leave the niche, necessitating an additional mechanism to compensate for this loss and maintain a constant number of GSCs. Dedifferentiation and symmetric renewal have been shown to replenish lost GSCs during regenerative and physiological conditions. However, it remains unknown whether dedifferentiated GSCs reacquire native GSC behaviors. Using long-term live imaging, we trace the cells following dedifferentiation and show that dedifferentiated GSCs appear to reacquire at least one aspect of native GSC behavior, the centrosome orientation checkpoint, a GSC-specific checkpoint mechanism that ensures oriented spindle to achieve asymmetric stem cell divisions. Our findings provide important insights into the robust mechanisms ensuring asymmetric division in the niche.

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Publication Details

Journal
Communications Biology
Published
2026-03-09
DOI
https://doi.org/10.1038/s42003-026-09812-7
Primary Topic
Microtubule and mitosis dynamics
Type
article
Field-Weighted Citation Impact
0.00

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article

Stem cells resume asymmetric division upon niche re-entry through reactivating the centrosome orientation checkpoint

Autumn Twillie, Muhammed Burak Bener, Mayu Inaba, Naiya Patel
Communications Biology
Microtubule and mitosis dynamics
article

Stem cells resume asymmetric division upon niche re-entry through reactivating the centrosome orientation checkpoint

Autumn Twillie, Muhammed Burak Bener, Mayu Inaba, Naiya Patel
article en

Abstract

In Drosophila testis, germline stem cells (GSCs) typically divide asymmetrically, keeping one daughter cell within the niche for self-renewal and placing the other daughter cell outside the niche to undergo differentiation. This is the primary mechanism for maintaining a stable number of stem cells in the niche. However, it has been shown that small fraction of GSCs continuously leave the niche, necessitating an additional mechanism to compensate for this loss and maintain a constant number of GSCs. Dedifferentiation and symmetric renewal have been shown to replenish lost GSCs during regenerative and physiological conditions. However, it remains unknown whether dedifferentiated GSCs reacquire native GSC behaviors. Using long-term live imaging, we trace the cells following dedifferentiation and show that dedifferentiated GSCs appear to reacquire at least one aspect of native GSC behavior, the centrosome orientation checkpoint, a GSC-specific checkpoint mechanism that ensures oriented spindle to achieve asymmetric stem cell divisions. Our findings provide important insights into the robust mechanisms ensuring asymmetric division in the niche.

Communications Biology
UConn Health (US)
University of Connecticut Health Center
Openalex Percentile: Top 29%
Microtubule and mitosis dynamics
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