Day-night cycles and the sleep-promoting factor, Sleepless, affect stem cell activity in the Drosophila testis

Proc Natl Acad Sci U S A. 2014 Feb 25;111(8):3026-31. doi: 10.1073/pnas.1316552111. Epub 2014 Feb 10.

Abstract

Adult stem cells maintain tissue integrity and function by renewing cellular content of the organism through regulated mitotic divisions. Previous studies showed that stem cell activity is affected by local, systemic, and environmental cues. Here, we explore a role of environmental day-night cycles in modulating cell cycle progression in populations of adult stem cells. Using a classic stem cell system, the Drosophila spermatogonial stem cell niche, we reveal daily rhythms in division frequencies of germ-line and somatic stem cells that act cooperatively to produce male gametes. We also examine whether behavioral sleep-wake cycles, which are driven by the environmental day-night cycles, regulate stem cell function. We find that flies lacking the sleep-promoting factor Sleepless, which maintains normal sleep in Drosophila, have increased germ-line stem cell (GSC) division rates, and this effect is mediated, in part, through a GABAergic signaling pathway. We suggest that alterations in sleep can influence the daily dynamics of GSC divisions.

Keywords: environmental cycles; sleep duration; stem cell regulation; tissue homeostasis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult Stem Cells / physiology*
  • Animals
  • Bromodeoxyuridine
  • Circadian Rhythm / physiology*
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Drosophila / physiology*
  • Drosophila Proteins / metabolism*
  • GABAergic Neurons / metabolism
  • Germ Cells / physiology
  • Homeostasis / physiology
  • Isonicotinic Acids
  • Male
  • Membrane Proteins / metabolism*
  • Mifepristone
  • Signal Transduction / physiology
  • Sleep / physiology*
  • Testis / cytology*
  • Testis / metabolism

Substances

  • Drosophila Proteins
  • Isonicotinic Acids
  • Membrane Proteins
  • Qvr protein, Drosophila
  • Mifepristone
  • Cyclic AMP-Dependent Protein Kinases
  • Bromodeoxyuridine
  • isoguvacine