Membrane Repair Defects in Muscular Dystrophy Are Linked to Altered Interaction between MG53, Caveolin-3, and Dysferlin

Abstract

Defective membrane repair can contribute to the progression of muscular dystrophy. Although mutations in caveolin-3 (Cav3) and dysferlin are linked to muscular dystrophy in human patients, the molecular mechanism underlying the functional interplay between Cav3 and dysferlin in membrane repair of muscle physiology and disease has not been fully resolved. We recently discovered that mitsugumin 53 (MG53), a muscle-specific TRIM (Tri-partite motif) family protein (TRIM72), contributes to intracellular vesicle trafficking and is an essential component of the membrane repair machinery in striated muscle. Here we show that MG53 interacts with dysferlin and Cav3 to regulate membrane repair in skeletal muscle. MG53 mediates active trafficking of intracellular vesicles to the sarcolemma and is required for movement of dysferlin to sites of cell injury during repair patch formation. Mutations in Cav3 (P104L, R26Q) that cause retention of Cav3 in Golgi apparatus result in aberrant localization of MG53 and dysferlin in a dominant-negative fashion, leading to defective membrane repair. Our data reveal that a molecular complex formed by MG53, dysferlin, and Cav3 is essential for repair of muscle membrane damage and also provide a therapeutic target for treatment of muscular and cardiovascular diseases that are linked to compromised membrane repair.Membrane recycling and remodeling contribute to multiple cellular functions, including cell fusion events during myogenesis and maintenance of sarcolemma integrity in striated muscle. During the life cycle of striated muscle, membrane repair is a fundamental process in maintaining cellular integrity, as shown by recent studies that link defective membrane repair to the progression of muscular dystrophy (1-3). Repair of the plasma membrane damage requires recruitment of intracellular vesicles to injury sites (4, 5). One protein that has been linked to membrane repair in skeletal muscle is dysferlin (6, 7), which is thought to fuse intracellular vesicles to patch the damaged membrane and restore sarcolemmal integrity following muscle injury. Like dysferlin, caveolin-3 (Cav3) 3 is a muscle-specific protein, and many mutations in Cav3, including P104L, R26Q, and C71W, have been linked to muscular dystrophy (8 -11). Despite extensive research efforts on Cav3 and dysferlin (12)(13)(14), the molecular function of these two proteins in membrane repair in muscle physiology and dystrophy have not been fully defined.Animal model studies reveal that either loss or gain of Cav3 function both result in dystrophic phenotypes in skeletal muscle (15, 16), suggesting that associated cellular components may be involved in the etiology of Cav3-related dystrophy. Although the discovery of dysferlin highlights the importance of membrane repair in the etiology of muscular dystrophy, dysferlin itself does not appear to participate in recruitment of intracellular vesicles because dysferlin Ϫ/Ϫ muscle retains accumulation of vesicles near membrane damage sites (7). This indicates that proteins other than dys...

Dysferlin stabilizes stress-induced Ca 2+ signaling in the transverse tubule membrane

“…However, the ability of laser wounding to predict the outcome of interventional treatments for dysferlinopathies has been recently questioned (39). Furthermore, recent evidence suggests that dysferlin, although recruited to the wounded sarcolemma (3), is not necessary for the immediate resealing of the damaged sarcolemmal membrane following laser wounding (40,41) or large-strain lengthening contractions (20).…”

Genetic Manipulation of Dysferlin Expression in Skeletal Muscle

“…Dysferlin interacts with a number of other proteins that could affect the health of the membrane such as annexins, AHNAK, and MG53, which have also been implicated in membrane trafficking and resealing. [17][18][19][20] Dysferlin also interacts with affixin, a focal adhesion protein, the L-type calcium channel, caveolin 3, and calpain 3, the later two of which themselves can cause a limb-girdle MD when deficient. [21][22][23] Our results clearly show that replacement of dysferlin by transgenesis only in skeletal muscle of A/J mice completely rescued muscle pathology and fully restored functional recovery from injury caused by large strain lengthening contractions.…”

MicroRNA-21 regulation of the progression of viral myocarditis to dilated cardiomyopathy

“…They are subject to tight control at multiple levels, including differential localization, post-translational modification and the regulation of protein levels. SPRY participates in multiple physiological and pathological processes, including acute membrane repair, myogenesis in skeletal muscle and cardiac ischemic preconditioning (12,(15)(16)(17). Thum et al identified that SPRY1 was a direct target of miRNA-21 and mediated the effect of miRNA-21 in cardiac fibroblasts (18).…”