The overall goal of this proposal is to obtain an in-depth understanding of the mechanistic links between alterations of the dystrophin glycoprotein complex (DGC) and impairment of the excitation-contraction coupling (ECC) process in mammalian skeletal muscle. This functional characterization will be achieved in muscle fibers from various animal models of human muscular dystrophies. We have found that Ca2+ release evoked by action potentials (APs) (or voltage-clamp pulses) in muscle fibers from two of such models, the adult mdx mouse and the phenotypic sarcospan (SSPN) overexpressing mouse (SSPN-Tg), is significantly smaller than in wild type fibers. We hypothesize that disruption of the DGC undermines the structural and functional support for the transverse tubular system (TTS) and the sarcoplasmic reticulum (SR), thus attenuating the ECC process. We will first investigate the mechanisms responsible for the impairment of Ca2+ release in mdx mice (Aim 1), the most prevalently used animal model for Duchenne Muscular Dystrophy (DMD), which lacks dystrophin in the DGC. However, since the phenotypic alterations in mdx mice are relatively benign, possibly due to utrophin substitution in the DGC, experiments will be also carried out in double knockout mdx/utrophin (mdx/utr-/-) mice that display a phenotype more comparable to that in DMD patients (Aim 2). To further characterize the link between the DGC integrity and a fully functional ECC, we will take advantage of our ability to express DGC proteins by in vivo electroporation and use transgenic animal models with other genetic conditions altering the DGC (e.g. SSPN-Tg, and Utr-TET). The last goal of the proposal is to investigate, using 2-photon laser scanning microscopy (TPLSM) the subcellular distribution of representative DGC protein components in order to assess if they are associated exclusively with the sarcolemma or if they have a more ubiquitous distribution in association with the Z-line and the TTS. This characterization will help us understand the function of the DGC in terms of ECC and sarcolemmal integrity (Aim 3). These investigations will be carried out by using electrophysiological and state-of-the-art optical methods, such as F""""""""ster resonance energy transfer (FRET) and total internal reflection fluorescence microscopy (TIRFM), to also assess the nanoscale localization of DGC and ECC proteins with respect to the internal and external leaflets of the surface and TTS membranes.

Public Health Relevance

In Duchenne Muscular Dystrophy (DMD) the muscles lack the protein dystrophin, an integral component of a dystrophin-glycoprotein complex (DGC). We have discovered that the absence of dystrophin in the muscle fibers of the mdx mouse, a widely used animal model of DMD, impairs their ability to release Ca2+ from the sarcoplasmic reticulum in response to electrical stimulation, thus explaining the muscle weakness observed in the DGC pathology. We now propose to investigate the mechanisms that link DGC alterations with a deficient Ca2+ release. The results will significantly broaden our understanding of muscle disease mechanisms and will potentially provide therapeutic molecular tools which are deemed necessary for further advances in gene therapy.

National Institute of Health (NIH)
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Research Project (R01)
Project #
Application #
Study Section
Special Emphasis Panel (ZRG1-MOSS-L (07))
Program Officer
Nuckolls, Glen H
Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
University of California Los Angeles
Schools of Medicine
Los Angeles
United States
Zip Code
DiFranco, Marino; QuiƱonez, Marbella; Shieh, Perry et al. (2014) Action potential-evoked calcium release is impaired in single skeletal muscle fibers from heart failure patients. PLoS One 9:e109309
Zampighi, Guido A; Serrano, Raul; Vergara, Julio L (2014) A novel synaptic vesicle fusion path in the rat cerebral cortex: the ""saddle"" point hypothesis. PLoS One 9:e100710
DiFranco, Marino; Yu, Carl; QuiƱonez, Marbella et al. (2013) Age-dependent chloride channel expression in skeletal muscle fibres of normal and HSA(LR) myotonic mice. J Physiol 591:1347-71
DiFranco, Marino; Quinonez, Marbella; Vergara, Julio L (2012) The delayed rectifier potassium conductance in the sarcolemma and the transverse tubular system membranes of mammalian skeletal muscle fibers. J Gen Physiol 140:109-37
DiFranco, Marino; Herrera, Alvaro; Vergara, Julio L (2011) Chloride currents from the transverse tubular system in adult mammalian skeletal muscle fibers. J Gen Physiol 137:21-41
DiFranco, Marino; Tran, Philip; Quinonez, Marbella et al. (2011) Functional expression of transgenic 1sDHPR channels in adult mammalian skeletal muscle fibres. J Physiol 589:1421-42
Ermolova, Natalia; Kudryashova, Elena; DiFranco, Marino et al. (2011) Pathogenity of some limb girdle muscular dystrophy mutations can result from reduced anchorage to myofibrils and altered stability of calpain 3. Hum Mol Genet 20:3331-45
DiFranco, Marino; Vergara, Julio L (2011) The Na conductance in the sarcolemma and the transverse tubular system membranes of mammalian skeletal muscle fibers. J Gen Physiol 138:393-419
Capote, Joana; DiFranco, Marino; Vergara, Julio L (2010) Excitation-contraction coupling alterations in mdx and utrophin/dystrophin double knockout mice: a comparative study. Am J Physiol Cell Physiol 298:C1077-86
DiFranco, Marino; Quinonez, Marbella; Capote, Joana et al. (2009) DNA transfection of mammalian skeletal muscles using in vivo electroporation. J Vis Exp :

Showing the most recent 10 out of 17 publications