Results 1 to 10 of about 21,491 (246)

The Role of Impaired Mitochondrial Dynamics in MFN2-Mediated Pathology

open access: yesFrontiers in Cell and Developmental Biology, 2022
The Mitofusin 2 protein (MFN2), encoded by the MFN2 gene, was first described for its role in mediating mitochondrial fusion. However, MFN2 is now recognized to play additional roles in mitochondrial autophagy (mitophagy), mitochondrial motility, lipid ...
MASHIAT ZAMAN, Tim Shutt
exaly   +5 more sources

PGAM5 is an MFN2 phosphatase that plays an essential role in the regulation of mitochondrial dynamics

open access: yesCell Reports, 2023
Summary: Mitochondrial morphology is regulated by the post-translational modifications of the dynamin family GTPase proteins including mitofusin 1 (MFN1), MFN2, and dynamin-related protein 1 (DRP1).
Kaitlin Szederkenyi   +2 more
exaly   +3 more sources

Mfn2 regulates mitochondria-associated ER membranes to affect PCOS oocyte development

open access: yesEndocrine Connections, 2023
This study aimed to investigate the role of mitochondrial-related protein Mfn2 in polycystic ovary syndrome (PCOS) and its impact on oocyte development.
Xiuhua Liao   +7 more
doaj   +3 more sources

Mfn2-mediated mitochondrial fusion alleviates doxorubicin-induced cardiotoxicity with enhancing its anticancer activity through metabolic switch

open access: yesRedox Biology, 2022
Imbalanced mitochondrial dynamics including inhibited mitochondrial fusion is associated with cardiac dysfunction as well as tumorigenesis. This study sought to explore the effects of promoting mitochondrial fusion on doxorubicin(Dox)-induced ...
Mingge Ding, Min Jia, Feng Fu
exaly   +3 more sources

RIPK3-driven phosphorylation of MFN2 orchestrates endoplasmic reticulum-mitochondria interaction and cardiomyocyte stress responses [PDF]

open access: yesRedox Biology
Background: Recent studies have demonstrated that necroptosis is one of the main forms of cardiomyocyte death in heart diseases. However, the crosstalk between the death-receptor necroptosis pathway and the mitochondrial necroptosis pathway remains ...
Yu Wang   +9 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

A human mitofusin 2 mutation can cause mitophagic cardiomyopathy

open access: yeseLife, 2023
Cardiac muscle has the highest mitochondrial density of any human tissue, but mitochondrial dysfunction is not a recognized cause of isolated cardiomyopathy. Here, we determined that the rare mitofusin (MFN) 2 R400Q mutation is 15–20× over-represented in
Antonietta Franco   +12 more
doaj   +1 more source

Mesenchymal stem cell-derived microvesicles improve intestinal barrier function by restoring mitochondrial dynamic balance in sepsis rats

open access: yesStem Cell Research & Therapy, 2021
Background Sepsis is a major cause of death in ICU, and intestinal barrier dysfunction is its important complication, while the treatment is limited. Recently, mesenchymal stem cell-derived microvesicles (MMVs) attract much attention as a strategy of ...
Danyang Zheng   +7 more
doaj   +1 more source

Involvement of Mfn2, Bcl2/Bax signaling and mitochondrial viability in the potential protective effect of Royal jelly against mitochondria-mediated ovarian apoptosis by cisplatin in rats [PDF]

open access: yesIranian Journal of Basic Medical Sciences, 2020
Objective(s): The current study aimed to assess cisplatin-mediated ovarian apoptosis in a rat model by Royal jelly (RJ). Materials and Methods: Thirty female adult albino rats (180-200 g) were divided into three groups (n=10): saline (0.9% NaCl, IP) was ...
khalid Hashem   +3 more
doaj   +1 more source

Characterization of a novel variant in the HR1 domain of MFN2 in a patient with ataxia, optic atrophy and sensorineural hearing loss [version 2; peer review: 2 approved, 1 approved with reservations]

open access: yesF1000Research, 2022
Background: Pathogenic variants in MFN2 cause Charcot-Marie-Tooth disease (CMT) type 2A (CMT2A) and are the leading cause of the axonal subtypes of CMT.
Davide Martino   +8 more
doaj   +1 more source

Home - About - Disclaimer - Privacy