Results 1 to 10 of about 22,079 (142)

Integrated bioinformatic and in vivo analysis confirms the cardioprotective role of OPA1 [PDF]

open access: yesBMC Cardiovascular Disorders
Background OPA1 is an inner mitochondrial membrane protein that mediates diverse signaling processes. OPA1 is important for cardiac function and protects against cardiac insults such as ischemia/reperfusion injury.
Claire Fong-McMaster   +15 more
doaj   +2 more sources

Effects of Mitochondrial Dynamics in the Pathophysiology of Obesity

open access: yesFrontiers in Bioscience-Landmark, 2022
Obesity has become an urgent and serious public health challenge with an overwhelming increase over the decades worldwide. The rate of obese children and adolescents has recently accelerated, especially in China.
Jinling Wang   +6 more
doaj   +1 more source

Adipose tissue-specific ablation of PGC-1β impairs thermogenesis in brown fat

open access: yesDisease Models & Mechanisms, 2022
Impaired thermogenesis observed in mice with whole-body ablation of peroxisome proliferator-activated receptor-γ coactivator-1β (PGC-1β; officially known as PPARGC1B) may result from impaired brown fat (brown adipose tissue; BAT) function, but other ...
Jiří Funda   +10 more
doaj   +1 more source

The mitochondrial fusion protein OPA1 is dispensable in the liver and its absence induces mitohormesis to protect liver from drug-induced injury

open access: yesNature Communications, 2023
Mitochondria are critical for metabolic homeostasis of the liver, and their dysfunction is a major cause of liver diseases. Optic atrophy 1 (OPA1) is a mitochondrial fusion protein with a role in cristae shaping.
Hakjoo Lee   +9 more
doaj   +1 more source

OPA1-Exon4b modulates the migration and invasion of hepatocellular carcinoma cells by ATP regulation

open access: yesMitochondrial Communications, 2023
Optic Atrophy 1 (OPA1), a mitochondrial inner protein, is involved in both mitochondrial fusion dynamic and cell apoptosis. OPA1 Exon4b (OPA1-Exon4b) was reported to be downregulated in hepatocellular carcinoma (HCC).
Haite Tang   +7 more
doaj   +1 more source

OPA1 Modulates Mitochondrial Ca2+ Uptake Through ER-Mitochondria Coupling

open access: yesFrontiers in Cell and Developmental Biology, 2022
Autosomal Dominant Optic Atrophy (ADOA), a disease that causes blindness and other neurological disorders, is linked to OPA1 mutations. OPA1, dependent on its GTPase and GED domains, governs inner mitochondrial membrane (IMM) fusion and cristae ...
Benjamín Cartes-Saavedra   +11 more
doaj   +1 more source

Opa1 Prevents Apoptosis and Cisplatin-Induced Ototoxicity in Murine Cochleae

open access: yesFrontiers in Cell and Developmental Biology, 2021
Optic atrophy1 (OPA1) is crucial for inner mitochondrial membrane (IMM) fusion and essential for maintaining crista structure and mitochondrial morphology.
Tingting Dong   +9 more
doaj   +1 more source

Mitochondrial Fusion Via OPA1 and MFN1 Supports Liver Tumor Cell Metabolism and Growth

open access: yesCells, 2020
Metabolic reprogramming universally occurs in cancer. Mitochondria act as the hubs of bioenergetics and metabolism. The morphodynamics of mitochondria, comprised of fusion and fission processes, are closely associated with mitochondrial functions and are
Meng Li   +15 more
doaj   +1 more source

Berberine mitigates hepatic insulin resistance by enhancing mitochondrial architecture via the SIRT1/Opa1 signalling pathway

open access: yesActa Biochimica et Biophysica Sinica, 2022
The aberrant changes of fussion/fission-related proteins can trigger mitochondrial dynamics imbalance, which cause mitochondrial dysfunctions and result insulin resistance (IR).
Xu Jia   +9 more
doaj   +1 more source

CRISPR-Cas9 correction of OPA1 c.1334G>A: p.R445H restores mitochondrial homeostasis in dominant optic atrophy patient-derived iPSCs

open access: yesMolecular Therapy: Nucleic Acids, 2021
Autosomal dominant optic atrophy (DOA) is the most common inherited optic neuropathy in the United Kingdom. DOA has an insidious onset in early childhood, typically presenting with bilateral, central visual loss caused by the preferential loss of retinal
Paul E. Sladen   +7 more
doaj   +1 more source

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