Abstract：
:Several lines of evidence suggest that mitochondrial dysfunction plays a critical role in the pathogenesis of microvascular complications of diabetes, including diabetic nephropathy. However, the signaling pathways by which hyperglycemia leads to mitochondrial dysfunction are not fully understood. Here we examined the role of Rho-associated coiled coil-containing protein kinase 1 (ROCK1) on mitochondrial dynamics by generating two diabetic mouse models with targeted deletions of ROCK1 and an inducible podocyte-specific knockin mouse expressing a constitutively active (cA) mutant of ROCK1. Our findings suggest that ROCK1 mediates hyperglycemia-induced mitochondrial fission by promoting dynamin-related protein-1 (Drp1) recruitment to the mitochondria. Deletion of ROCK1 in diabetic mice prevented mitochondrial fission, whereas podocyte-specific cA-ROCK1 mice exhibited increased mitochondrial fission. Importantly, we found that ROCK1 triggers mitochondrial fission by phosphorylating Drp1 at serine 600 residue. These findings provide insights into the unexpected role of ROCK1 in a signaling cascade that regulates mitochondrial dynamics.
journal_name
Cell Metabjournal_title
Cell metabolismauthors
Wang W,Wang Y,Long J,Wang J,Haudek SB,Overbeek P,Chang BH,Schumacker PT,Danesh FRdoi
10.1016/j.cmet.2012.01.009subject
Has Abstractpub_date
2012-02-08 00:00:00pages
186-200issue
2eissn
1550-4131issn
1932-7420pii
S1550-4131(12)00013-7journal_volume
15pub_type
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