Intestinal Stem Cell Pool Regulation in Drosophila

Stem Cell Reports. 2017 Jun 6;8(6):1479-1487. doi: 10.1016/j.stemcr.2017.04.002. Epub 2017 May 4.


Intestinal epithelial renewal is mediated by intestinal stem cells (ISCs) that exist in a state of neutral drift, wherein individual ISC lineages are regularly lost and born but ISC numbers remain constant. To test whether an active mechanism maintains stem cell pools in the Drosophila midgut, we performed partial ISC depletion. In contrast to the mouse intestine, Drosophila ISCs failed to repopulate the gut after partial depletion. Even when the midgut was challenged to regenerate by infection, ISCs retained normal proportions of asymmetric division and ISC pools did not increase. We discovered, however, that the loss of differentiated midgut enterocytes (ECs) slows when ISC division is suppressed and accelerates when ISC division increases. This plasticity in rates of EC turnover appears to facilitate epithelial homeostasis even after stem cell pools are compromised. Our study identifies unique behaviors of Drosophila midgut cells that maintain epithelial homeostasis.

Keywords: Drosophila; epithelial turnover; intestinal stem cell; midgut; neutral drift; stem cell behavior; stem cell pool.

MeSH terms

  • Animals
  • Cell Proliferation
  • Cells, Cultured
  • Drosophila
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism
  • Enterocytes / cytology
  • Enterocytes / drug effects
  • Enterocytes / metabolism
  • Intestines / cytology*
  • Kanamycin / toxicity
  • Pseudomonas / pathogenicity
  • Receptors, Notch / genetics
  • Receptors, Notch / metabolism
  • Regeneration / physiology
  • Signal Transduction
  • Stem Cells / cytology
  • Stem Cells / drug effects
  • Stem Cells / metabolism*
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism


  • Drosophila Proteins
  • N protein, Drosophila
  • Receptors, Notch
  • Tumor Suppressor Protein p53
  • esg protein, Drosophila
  • Kanamycin