Results 1 to 10 of about 16,238 (247)

Mitofusin 2 displays fusion-independent roles in proteostasis surveillance [PDF]

open access: goldNature Communications
Mitochondria are essential organelles and their functional state dictates cellular proteostasis. However, little is known about the molecular gatekeepers involved, especially in absence of external stress.
Mariana Joaquim   +18 more
doaj   +5 more sources

A human mitofusin 2 mutation can cause mitophagic cardiomyopathy [PDF]

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   +5 more sources

Mitochonic acid 5 regulates mitofusin 2 to protect microglia [PDF]

open access: yesNeural Regeneration Research, 2021
Microglial apoptosis is associated with neuroinflammation and no effective strategies are currently available to protect microglia against inflammation-induced apoptosis.
Jian Tan   +7 more
doaj   +4 more sources

Mitofusin-2 Negatively Regulates Melanogenesis by Modulating Mitochondrial ROS Generation [PDF]

open access: goldCells, 2022
Inter-organellar communication is emerging as one of the most crucial regulators of cellular physiology. One of the key regulators of inter-organellar communication is Mitofusin-2 (MFN2).
Jyoti Tanwar   +12 more
doaj   +4 more sources

Mitofusin-2 independent juxtaposition of endoplasmic reticulum and mitochondria: an ultrastructural study. [PDF]

open access: goldPLoS ONE, 2012
Besides its role in controlling the morphology of mitochondria, mitofusin-2 has been proposed to tether mitochondria to the endoplasmic reticulum (ER), based largely on light microscopic analysis. In this study we have examined by electron microscopy the
Pierre Cosson   +3 more
doaj   +3 more sources

Mice Hemizygous for a Pathogenic Mitofusin-2 Allele Exhibit Hind Limb/Foot Gait Deficits and Phenotypic Perturbations in Nerve and Muscle. [PDF]

open access: yesPLoS ONE, 2016
Charcot-Marie-Tooth disease type 2A (CMT2A), the most common axonal form of hereditary sensory motor neuropathy, is caused by mutations of mitofusin-2 (MFN2). Mitofusin-2 is a GTPase required for fusion of mitochondrial outer membranes, repair of damaged
Peter Bannerman   +4 more
doaj   +15 more sources

Mitofusin 2, a key coordinator between mitochondrial dynamics and innate immunity [PDF]

open access: yesVirulence, 2021
Remodeling of mitochondrial dynamics and mitochondrial morphology plays a pivotal role in the maintenance of mitochondrial homeostasis in response to pathogenic attacks or stress stimuli.
In Soo Kim   +2 more
doaj   +2 more sources

The role of Mitofusin-1 and Mitofusin-2 in periodontal disease: a comprehensive review [PDF]

open access: yesFrontiers in Oral Health
Periodontal disease is a widespread chronic inflammatory state influencing the supporting anatomy of the teeth, distinguished by oxidative stress, progressive bone loss, and tissue damage.
Sudhir R. Varma   +6 more
doaj   +2 more sources

Assessing the effects of mitofusin 2 deficiency in the adult heart using 3D electron tomography [PDF]

open access: gold, 2017
The effects of mitofusin 2 (MFN2) deficiency, on mitochondrial morphology and the mitochondria-junctional sarcoplasmic reticulum (jSR) complex in the adult heart, have been previously investigated using 2D electron microscopy, an approach which is unable
Cabrera-Fuentes, Hector   +12 more
core   +3 more sources

Presenilin 2 Modulates Endoplasmic Reticulum-Mitochondria Coupling by Tuning the Antagonistic Effect of Mitofusin 2 [PDF]

open access: goldCell Reports, 2016
Communication between organelles plays key roles in cell biology. In particular, physical and functional coupling of the endoplasmic reticulum (ER) and mitochondria is crucial for regulation of various physiological and pathophysiological processes. Here,
Riccardo Filadi   +5 more
doaj   +2 more sources

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