Literature DB >> 7805568

Mitochondrial Ca2+ transport and the role of intramitochondrial Ca2+ in the regulation of energy metabolism.

J G McCormack1, R M Denton.   

Abstract

The mitochondrial inner membrane of all mammalian tissues, including brain tissues, has specific active transport systems for the uptake and egress of Ca2+. The primary role of this transport system is to relay changes in cytosolic [Ca2+], which stimulates energy-requiring processes in the cytosol (e.g. secretion), into the mitochondrial matrix where it stimulates several key steps in energy production. Thus using the same second-messenger molecule, the latter events allow energetic homeostasis to be maintained under conditions of cell stimulation. This appears to be brought about by a co-ordinated enhancement of steps throughout the pathways of oxidative phosphorylation, including substrate supply to the respiratory chain by dehydrogenase activation, activation of the respiratory chain itself by a mechanism which appears to involve changes in the matrix volume, and also possibly activation of the ATP synthetase where the release of a specific inhibitory subunit has been proposed.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 7805568     DOI: 10.1159/000111332

Source DB:  PubMed          Journal:  Dev Neurosci        ISSN: 0378-5866            Impact factor:   2.984


  53 in total

1.  Increased propensity for cell death in diabetic human heart is mediated by mitochondrial-dependent pathways.

Authors:  Ethan J Anderson; Evelio Rodriguez; Curtis A Anderson; Kathleen Thayne; W Randolph Chitwood; Alan P Kypson
Journal:  Am J Physiol Heart Circ Physiol       Date:  2010-11-12       Impact factor: 4.733

2.  Genetic ablation of calcium-independent phospholipase A(2)γ (iPLA(2)γ) attenuates calcium-induced opening of the mitochondrial permeability transition pore and resultant cytochrome c release.

Authors:  Sung Ho Moon; Christopher M Jenkins; Michael A Kiebish; Harold F Sims; David J Mancuso; Richard W Gross
Journal:  J Biol Chem       Date:  2012-07-09       Impact factor: 5.157

Review 3.  Huntington's Disease and Mitochondria.

Authors:  Mohammad Jodeiri Farshbaf; Kamran Ghaedi
Journal:  Neurotox Res       Date:  2017-06-21       Impact factor: 3.911

Review 4.  Crosstalk between calcium and reactive oxygen species signaling in cancer.

Authors:  Nadine Hempel; Mohamed Trebak
Journal:  Cell Calcium       Date:  2017-01-18       Impact factor: 6.817

5.  Mitochondrial calcium buffering contributes to the maintenance of Basal calcium levels in mouse taste cells.

Authors:  Kyle Hacker; Kathryn F Medler
Journal:  J Neurophysiol       Date:  2008-08-06       Impact factor: 2.714

Review 6.  Calcium, energy metabolism and the development of selective neuronal loss following short-term cerebral ischemia.

Authors:  N R Sims
Journal:  Metab Brain Dis       Date:  1995-09       Impact factor: 3.584

7.  CRYAB and HSPB2 deficiency alters cardiac metabolism and paradoxically confers protection against myocardial ischemia in aging mice.

Authors:  Ivor J Benjamin; Yiru Guo; Sathyanarayanan Srinivasan; Sihem Boudina; Ryan P Taylor; Namakkal S Rajasekaran; Roberta Gottlieb; Eric F Wawrousek; E Dale Abel; Roberto Bolli
Journal:  Am J Physiol Heart Circ Physiol       Date:  2007-09-14       Impact factor: 4.733

Review 8.  Mitochondria-Associated Endoplasmic Reticulum Membranes (MAMs) and Their Prospective Roles in Kidney Disease.

Authors:  Peng Gao; Wenxia Yang; Lin Sun
Journal:  Oxid Med Cell Longev       Date:  2020-09-03       Impact factor: 6.543

9.  NCLX: the mitochondrial sodium calcium exchanger.

Authors:  Liron Boyman; George S B Williams; Daniel Khananshvili; Israel Sekler; W J Lederer
Journal:  J Mol Cell Cardiol       Date:  2013-03-26       Impact factor: 5.000

Review 10.  Mitochondrial reactive oxygen species production in excitable cells: modulators of mitochondrial and cell function.

Authors:  David F Stowe; Amadou K S Camara
Journal:  Antioxid Redox Signal       Date:  2009-06       Impact factor: 8.401

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.