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PGC-1α protects from myocardial ischaemia-reperfusion injury by regulating mitonuclear communication.
Li, Yan-Qing; Jiao, Yan; Liu, Ya-Nan; Fu, Jia-Ying; Sun, Lian-Kun; Su, Jing.
Afiliação
  • Li YQ; Department of Pathophysiology, College of Basic Medical Sciences, Jilin University, Changchun, China.
  • Jiao Y; Department of Hepatobiliary and Pancreatic Surgery, The First Hospital of Jilin University, Changchun, China.
  • Liu YN; Department of Pathophysiology, College of Basic Medical Sciences, Jilin University, Changchun, China.
  • Fu JY; Department of Pathophysiology, College of Basic Medical Sciences, Jilin University, Changchun, China.
  • Sun LK; Department of Pathophysiology, College of Basic Medical Sciences, Jilin University, Changchun, China.
  • Su J; Department of Pathophysiology, College of Basic Medical Sciences, Jilin University, Changchun, China.
J Cell Mol Med ; 26(3): 593-600, 2022 02.
Article em En | MEDLINE | ID: mdl-33470050
ABSTRACT
The recovery of blood supply after a period of myocardial ischaemia does not restore the heart function and instead results in a serious dysfunction called myocardial ischaemia-reperfusion injury (IRI), which involves several complex pathophysiological processes. Mitochondria have a wide range of functions in maintaining the cellular energy supply, cell signalling and programmed cell death. When mitochondrial function is insufficient or disordered, it may have adverse effects on myocardial ischaemia-reperfusion and therefore mitochondrial dysfunction caused by oxidative stress a core molecular mechanism of IRI. Peroxisome proliferator-activated receptor gamma co-activator 1α (PGC-1α) is an important antioxidant molecule found in mitochondria. However, its role in IRI has not yet been systematically summarized. In this review, we speculate the role of PGC-1α as a key regulator of mitonuclear communication, which may interacts with nuclear factor, erythroid 2 like -1 and -2 (NRF-1/2) to inhibit mitochondrial oxidative stress, promote the clearance of damaged mitochondria, enhance mitochondrial biogenesis, and reduce the burden of IRI.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Traumatismo por Reperfusão Miocárdica Limite: Humans Idioma: En Revista: J Cell Mol Med Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Traumatismo por Reperfusão Miocárdica Limite: Humans Idioma: En Revista: J Cell Mol Med Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China