4.7 Article

Apoptotic regulators promote cytokinetic midbody degradation in C. elegans

Journal

JOURNAL OF CELL BIOLOGY
Volume 199, Issue 7, Pages 1047-1055

Publisher

ROCKEFELLER UNIV PRESS
DOI: 10.1083/jcb.201209050

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Funding

  1. National Basic Research Program of China (973 Program) [2012CB966800, 2012CB945002, 2013CB945600]
  2. National Natural Science Foundation of China [31101002, 31100972, 31171295, 31190063, 31201009, 31222035]
  3. Junior Thousand Talents Program of China

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Cell death genes are essential for apoptosis and other cellular events, but their nonapoptotic functions are not well understood. The midbody is an important cytokinetic structure required for daughter cell abscission, but its fate after cell division remains elusive in metazoans. In this paper, we show through live-imaging analysis that midbodies generated by Q cell divisions in Caenorhabditis elegans were released to the extracellular space after abscission and subsequently internalized and degraded by the phagocyte that digests apoptotic Q cell corpses. We further show that midbody degradation is defective in apoptotic cell engulfment mutants. Externalized phosphatidylserine (PS), an engulfment signal for corpse phagocytosis, exists on the outer surface of the midbody, and inhibiting PS signaling delayed midbody clearance. Thus, our findings uncover a novel function of cell death genes in midbody internalization and degradation after cell division.

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