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Difference between revisions of "Diebold 2019 Nat Metab"

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(Created page with "{{Publication |title=Diebold LP, Gil HJ, Gao P, Martinez CA, Weinberg SE, Chandel NS (2019) Mitochondrial Complex III is necessary for endothelial cell proliferation during an...")
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{{Publication
|title=Diebold LP, Gil HJ, Gao P, Martinez CA, Weinberg SE, Chandel NS (2019) Mitochondrial Complex III is necessary for endothelial cell proliferation during angiogenesis. Nat Metab 1:158–71.
|title=Diebold LP, Gil HJ, Gao P, Martinez CA, Weinberg SE, Chandel NS (2019) Mitochondrial Complex III is necessary for endothelial cell proliferation during angiogenesis. Nat Metab 1:158–71.
|info=[https://www.nature.com/articles/s42255-018-0011-x Nat Metab Open Access]
|info=[https://www.ncbi.nlm.nih.gov/pubmed/31106291 PMID: 31106291 Open Access]
|authors=Diebold LP, Gil HJ, Gao P, Martinez CA, Weinberg SE, Chandel NS
|authors=Diebold LP, Gil HJ, Gao P, Martinez CA, Weinberg SE, Chandel NS
|year=2019
|year=2019

Revision as of 14:00, 15 October 2019

Publications in the MiPMap
Diebold LP, Gil HJ, Gao P, Martinez CA, Weinberg SE, Chandel NS (2019) Mitochondrial Complex III is necessary for endothelial cell proliferation during angiogenesis. Nat Metab 1:158–71.

Β» PMID: 31106291 Open Access

Diebold LP, Gil HJ, Gao P, Martinez CA, Weinberg SE, Chandel NS (2019) Nat Metab

Abstract: Endothelial cells (ECs) require glycolysis for proliferation and migration during angiogenesis; however, the necessity for the mitochondrial respiratory chain during angiogenesis is not known. Here we report that inhibition of respiratory chain Complex III impairs proliferation, but not migration, of ECs in vitro by decreasing the NAD+/NADH ratio. To determine whether mitochondrial respiration is necessary for angiogenesis in vivo, we conditionally ablate a subunit of the respiratory chain Complex III (QPC) in ECs. Loss of QPC decreases respiration, resulting in diminished EC proliferation, and impairment in retinal and tumour angiogenesis. Loss of QPC does not decrease genes associated with anabolism or nucleotide levels in ECs but diminishes amino acid levels. Our findings indicate that mitochondrial respiration is necessary for angiogenesis and that the primary role of mitochondria in ECs is to serve as biosynthetic organelles for cell proliferation.

β€’ Bioblast editor: Gnaiger E


Labels: MiParea: Respiration  Pathology: Cancer 

Organism: Human  Tissue;cell: HUVEC  Preparation: Intact cells 


Coupling state: LEAK, ROUTINE  Pathway: ROX