Endoplasmic reticulum-specific BH3-only protein BNIP1 induces mitochondrial fragmentation in a Bcl-2- and Drp1-dependent manner

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Bcl-2/adenovirus E1B 19-kDa interacting protein 1 (BNIP1), which is predominantly localized to the endoplasmic reticulum (ER), is a pro-apoptotic Bcl-2 homology domain 3 (BH3)-only protein. Here, we show that the expression of BNIP1 induced not only a highly interconnected ER network but also mitochondrial fragmentation in a BH3 domain-dependent manner. Functional analysis demonstrated that BNIP1 expression increased dynamin-related protein 1 (Drp1) expression followed by the mitochondrial translocation of Drp1 and subsequent mitochondrial fission. Both BNIP1-induced mitochondrial fission and the translocation of Drp1 were abrogated by Bcl-2 overexpression. These results collectively indicate that ER-specific BNIP1 plays an important role in mitochondrial dynamics by modulating the mitochondrial fission protein Drp1 in a BH3 domain-dependent fashion. J. Cell. Physiol. 227: 30273035, 2012. (c) 2011 Wiley Periodicals, Inc.
Publisher
WILEY-BLACKWELL
Issue Date
2012-08
Language
English
Article Type
Article
Keywords

CYTOCHROME-C RELEASE; CELL-DEATH; APOPTOSIS; DRP1; MORPHOLOGY; FISSION; PHOSPHORYLATION; FUSION; FAMILY; DYNAMICS

Citation

JOURNAL OF CELLULAR PHYSIOLOGY, v.227, no.8, pp.3027 - 3035

ISSN
0021-9541
DOI
10.1002/jcp.23044
URI
http://hdl.handle.net/10203/103226
Appears in Collection
BS-Journal Papers(저널논문)BiS-Journal Papers(저널논문)
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