Mitochondrial fission regulates germ cell differentiation by suppressing ROS-mediated activation of Epidermal Growth Factor Signaling in the Drosophila larval testis.
Rafael Sênos DemarcoD Leanne JonesPublished in: Scientific reports (2019)
Mitochondria are essential organelles that have recently emerged as hubs for several metabolic and signaling pathways in the cell. Mitochondrial morphology is regulated by constant fusion and fission events to maintain a functional mitochondrial network and to remodel the mitochondrial network in response to external stimuli. Although the role of mitochondria in later stages of spermatogenesis has been investigated in depth, the role of mitochondrial dynamics in regulating early germ cell behavior is relatively less-well understood. We previously demonstrated that mitochondrial fusion is required for germline stem cell (GSC) maintenance in the Drosophila testis. Here, we show that mitochondrial fission is also important for regulating the maintenance of early germ cells in larval testes. Inhibition of Drp1 in early germ cells resulted in the loss of GSCs and spermatogonia due to the accumulation of reactive oxygen species (ROS) and activation of the EGFR pathway in adjacent somatic cyst cells. EGFR activation contributed to premature germ cell differentiation. Our data provide insights into how mitochondrial dynamics can impact germ cell maintenance and differentiation via distinct mechanisms throughout development.
Keyphrases
- germ cell
- oxidative stress
- induced apoptosis
- reactive oxygen species
- stem cells
- growth factor
- small cell lung cancer
- cell death
- cell cycle arrest
- signaling pathway
- epidermal growth factor receptor
- cell proliferation
- single molecule
- electronic health record
- bone marrow
- optical coherence tomography
- mass spectrometry
- dna methylation
- endoplasmic reticulum
- atomic force microscopy