Membrane repair defects in muscular dystrophy are linked to altered interaction between MG53, caveolin-3, and dysferlin
about
Reduced plasma membrane expression of dysferlin mutants is attributed to accelerated endocytosis via a syntaxin-4-associated pathwayAlternate splicing of dysferlin C2A confers Ca²⁺-dependent and Ca²⁺-independent binding for membrane repairAssembly and Turnover of Caveolae: What Do We Really Know?Damage control: cellular mechanisms of plasma membrane repairFerlins: regulators of vesicle fusion for auditory neurotransmission, receptor trafficking and membrane repairThe caveolin-cavin system plays a conserved and critical role in mechanoprotection of skeletal muscle.Dysferlin-peptides reallocate mutated dysferlin thereby restoring functionAnnexin-A5 assembled into two-dimensional arrays promotes cell membrane repairAbove the fray: Surface remodeling by secreted lysosomal enzymes leads to endocytosis-mediated plasma membrane repairEnhancing muscle membrane repair by gene delivery of MG53 ameliorates muscular dystrophy and heart failure in δ-Sarcoglycan-deficient hamsters.Nonmuscle myosin IIA facilitates vesicle trafficking for MG53-mediated cell membrane repair.Recombinant MG53 protein modulates therapeutic cell membrane repair in treatment of muscular dystrophyRapid actin-cytoskeleton-dependent recruitment of plasma membrane-derived dysferlin at wounds is critical for muscle membrane repair.Mitsugumin 53 regulates extracellular Ca(2+) entry and intracellular Ca(2+) release via Orai1 and RyR1 in skeletal muscle.Comparison of dysferlin expression in human skeletal muscle with that in monocytes for the diagnosis of dysferlin myopathy.Sarcolemmal repair is a slow process and includes EHD2.Dysferlin interacts with tubulin and microtubules in mouse skeletal muscle.Effect of recombinant human MG53 protein on tourniquet-induced ischemia-reperfusion injury in rat muscleRecessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies.Proteomic analysis of the dysferlin protein complex unveils its importance for sarcolemmal maintenance and integrityIL-1α reversibly inhibits skeletal muscle ryanodine receptor. a novel mechanism for critical illness myopathy?Partial dysferlin reconstitution by adult murine mesoangioblasts is sufficient for full functional recovery in a murine model of dysferlinopathy.Expression levels of sarcolemmal membrane repair proteins following prolonged exercise training in miceTreatment of acute lung injury by targeting MG53-mediated cell membrane repair.Dysferlin interacts with histone deacetylase 6 and increases alpha-tubulin acetylationContribution of dysferlin deficiency to skeletal muscle pathology in asymptomatic and severe dystroglycanopathy models: generation of a new model for Fukuyama congenital muscular dystrophyTRIM72 is required for effective repair of alveolar epithelial cell wounding.An omega-3 fatty acid-enriched diet prevents skeletal muscle lesions in a hamster model of dystrophy.The intracellular Ca²⁺ channel MCOLN1 is required for sarcolemma repair to prevent muscular dystrophy.Modular dispensability of dysferlin C2 domains reveals rational design for mini-dysferlin molecules.Genetic ablation of complement C3 attenuates muscle pathology in dysferlin-deficient miceThe C2A domain in dysferlin is important for association with MG53 (TRIM72).The Sick and the Weak: Neuropathies/Myopathies in the Critically Ill.Calpain cleavage within dysferlin exon 40a releases a synaptotagmin-like module for membrane repair.Antisense therapy in neurologyPolymerase transcriptase release factor (PTRF) anchors MG53 protein to cell injury site for initiation of membrane repairMG53 participates in ischaemic postconditioning through the RISK signalling pathwayRedox-dependent oligomerization through a leucine zipper motif is essential for MG53-mediated cell membrane repairLoading-associated expression of TRIM72 and caveolin-3 in antigravitational soleus muscle in mice.T-tubule biogenesis and triad formation in skeletal muscle and implication in human diseases.
P2860
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P2860
Membrane repair defects in muscular dystrophy are linked to altered interaction between MG53, caveolin-3, and dysferlin
description
2009 nî lūn-bûn
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2009 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Membrane repair defects in mus ...... G53, caveolin-3, and dysferlin
@ast
Membrane repair defects in mus ...... G53, caveolin-3, and dysferlin
@en
Membrane repair defects in mus ...... G53, caveolin-3, and dysferlin
@nl
type
label
Membrane repair defects in mus ...... G53, caveolin-3, and dysferlin
@ast
Membrane repair defects in mus ...... G53, caveolin-3, and dysferlin
@en
Membrane repair defects in mus ...... G53, caveolin-3, and dysferlin
@nl
prefLabel
Membrane repair defects in mus ...... G53, caveolin-3, and dysferlin
@ast
Membrane repair defects in mus ...... G53, caveolin-3, and dysferlin
@en
Membrane repair defects in mus ...... G53, caveolin-3, and dysferlin
@nl
P2093
P2860
P921
P3181
P356
P1476
Membrane repair defects in mus ...... G53, caveolin-3, and dysferlin
@en
P2093
Chuanxi Cai
Jae-Kyun Ko
Jianjie Ma
Miyuki Nishi
Noah Weisleder
Shinji Komazaki
Yoshihide Sunada
P2860
P304
15894-15902
P3181
P356
10.1074/JBC.M109.009589
P407
P577
2009-04-20T00:00:00Z