Intrinsically determined cell death of developing cortical interneurons.

Published

Journal Article

Cortical inhibitory circuits are formed by γ-aminobutyric acid (GABA)-secreting interneurons, a cell population that originates far from the cerebral cortex in the embryonic ventral forebrain. Given their distant developmental origins, it is intriguing how the number of cortical interneurons is ultimately determined. One possibility, suggested by the neurotrophic hypothesis, is that cortical interneurons are overproduced, and then after their migration into cortex the excess interneurons are eliminated through a competition for extrinsically derived trophic signals. Here we characterize the developmental cell death of mouse cortical interneurons in vivo, in vitro and after transplantation. We found that 40% of developing cortical interneurons were eliminated through Bax (Bcl-2-associated X)-dependent apoptosis during postnatal life. When cultured in vitro or transplanted into the cortex, interneuron precursors died at a cellular age similar to that at which endogenous interneurons died during normal development. Over transplant sizes that varied 200-fold, a constant fraction of the transplanted population underwent cell death. The death of transplanted neurons was not affected by the cell-autonomous disruption of TrkB (tropomyosin kinase receptor B), the main neurotrophin receptor expressed by neurons of the central nervous system. Transplantation expanded the cortical interneuron population by up to 35%, but the frequency of inhibitory synaptic events did not scale with the number of transplanted interneurons. Taken together, our findings indicate that interneuron cell death is determined intrinsically, either cell-autonomously or through a population-autonomous competition for survival signals derived from other interneurons.

Full Text

Duke Authors

Cited Authors

  • Southwell, DG; Paredes, MF; Galvao, RP; Jones, DL; Froemke, RC; Sebe, JY; Alfaro-Cervello, C; Tang, Y; Garcia-Verdugo, JM; Rubenstein, JL; Baraban, SC; Alvarez-Buylla, A

Published Date

  • November 1, 2012

Published In

Volume / Issue

  • 491 / 7422

Start / End Page

  • 109 - 113

PubMed ID

  • 23041929

Pubmed Central ID

  • 23041929

Electronic International Standard Serial Number (EISSN)

  • 1476-4687

Digital Object Identifier (DOI)

  • 10.1038/nature11523

Language

  • eng

Conference Location

  • England