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  Mito-Morphosis: Mitochondrial Fusion, Fission, and Cristae Remodeling as Key Mediators of Cellular Function

Pernas, L., & Scorrano, L. (2016). Mito-Morphosis: Mitochondrial Fusion, Fission, and Cristae Remodeling as Key Mediators of Cellular Function. Annu Rev Physiol, 78, 505-31. doi:10.1146/annurev-physiol-021115-105011.

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Pernas, L.1, Author           
Scorrano, L., Author
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1Pernas – Metabolism of Infection, Max Planck Research Groups, Max Planck Institute for Biology of Ageing, Max Planck Society, ou_3394005              

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Free keywords: Animals Humans Membrane Fusion/*physiology Mitochondria/metabolism/*physiology Mitochondrial Dynamics/*physiology Mitochondrial Membranes/metabolism/physiology Mitochondrial Proteins/metabolism Drp1 Mfn1 Mfn2 Opa1 dynamin-related GTPases mitochondrial dynamics
 Abstract: Permanent residency in the eukaryotic cell pressured the prokaryotic mitochondrial ancestor to strategize for intracellular living. Mitochondria are able to autonomously integrate and respond to cellular cues and demands by remodeling their morphology. These processes define mitochondrial dynamics and inextricably link the fate of the mitochondrion and that of the host eukaryote, as exemplified by the human diseases that result from mutations in mitochondrial dynamics proteins. In this review, we delineate the architecture of mitochondria and define the mechanisms by which they modify their shape. Key players in these mechanisms are discussed, along with their role in manipulating mitochondrial morphology during cellular action and development. Throughout, we highlight the evolutionary context in which mitochondrial dynamics emerged and consider unanswered questions whose dissection might lead to mitochondrial morphology-based therapies.

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 Dates: 20162016
 Publication Status: Issued
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 Identifiers: Other: 26667075
DOI: 10.1146/annurev-physiol-021115-105011
ISSN: 1545-1585 (Electronic)0066-4278 (Linking)
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Title: Annu Rev Physiol
Source Genre: Journal
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Pages: - Volume / Issue: 78 Sequence Number: - Start / End Page: 505 - 31 Identifier: -