4.6 Article

Dynamin-Related Protein 1 Deficiency Leads to Receptor-Interacting Protein Kinase 3-Mediated Necroptotic Neurodegeneration

Journal

AMERICAN JOURNAL OF PATHOLOGY
Volume 186, Issue 11, Pages 2798-2802

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.ajpath.2016.06.025

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Funding

  1. NIH [GM084015, GM089853, NS084154]
  2. Johns Hopkins University Catalyst Award
  3. American Heart Association grant [15GRNT25380005]
  4. Johns Hopkins University School of Medicine Discovery Award

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Mitochondria are dynamic organelles that divide and fuse to modulate their number and shape. We have previously reported that the loss of dynamin-related protein 1 (Drp1.), which mediates mitochondrial division, leads to the degeneration of cerebellar Purkinje cells in mice. Because Drp1 has been shown to be important for apoptosis and necroptosis, it is puzzling how Purkinje neurons die in the absence of Drp1. In this study, we tested whether neurodegeneration involves necrotic cell death by generating Purkinje cell-specific Drp1-knockout (K0) mice that lack the receptor-interacting protein kinase 3 (Rip3), which regulates necroptosis. We found that the loss of Rip3 significantly delays the degeneration of Drp1-K0 Purkinje neurons. In addition, before neurodegeneration, mitochondrial tubules elongate because of unopposed fusion and subsequently become Large spheres as a result of oxidative damage. Surprisingly, Rip3 loss also helps Drp1-K0 Purkinje cells maintain the elongated morphology of the mitochondrial tubules. These data suggest that Rip3 plays a role in neurodegeneration and mitochondrial morphology in the absence of mitochondrial division.

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