4.8 Article

Spatiotemporal Control of CNS Myelination by Oligodendrocyte Programmed Cell Death through the TFEB-PUMA Axis

Journal

CELL
Volume 175, Issue 7, Pages 1811-+

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2018.10.044

Keywords

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Funding

  1. Helen Hay Whitney Foundation
  2. National Multiple Sclerosis Society career transition award [TA-1705-27634]
  3. NIH Pathway to Independence award [1K99EY029330]
  4. Vincent J. Coates Research Foundation
  5. Dr. Miriam and Sheldon G. Adelson Medical Research Foundation
  6. Myra Reinhard Family Foundation
  7. NIH [RO1 NS089786-05]
  8. Stanford Neuroscience Microscopy Service [NIH NS069375]
  9. Stanford Cell Sciences Imaging Facility [NCRR 1S10RR026780]
  10. Stanford Functional Genomic Facility [NIH S10OD018220]

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Nervous system function depends on proper myelination for insulation and critical trophic support for axons. Myelination is tightly regulated spatially and temporally, but how it is controlled molecularly remains largely unknown. Here, we identified key molecular mechanisms governing the regional and temporal specificity of CNS myelination. We show that transcription factor EB (TFEB) is highly expressed by differentiating oligodendrocytes and that its loss causes precocious and ectopic myelination in many parts of the murine brain. TFEB functions cell-autonomously through PUMA induction and Bax-Bak activation to promote programmed cell death of a subset of premyelinating oligodendrocytes, allowing selective elimination of oligodendrocytes in normally unmyelinated brain regions. This pathway is conserved across diverse brain areas and is critical for myelination timing. Our findings define an oligodendrocyte-intrinsic mechanism underlying the spatiotemporal specificity of CNS myelination, shedding light on how myelinating glia sculpt the nervous system during development.

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