| Literature DB >> 28012042 |
Vanessa Schartner1,2,3,4, Norma B Romero5,6, Sandra Donkervoort7, Susan Treves8,9, Pinki Munot10, Tyler Mark Pierson11,12, Ivana Dabaj13,14,15, Edoardo Malfatti5,6, Irina T Zaharieva10, Francesco Zorzato8,9, Osorio Abath Neto1,7, Guy Brochier5,6, Xavière Lornage1,2,3,4, Bruno Eymard16, Ana Lía Taratuto17, Johann Böhm1,2,3,4, Hernan Gonorazky18, Leigh Ramos-Platt19, Lucy Feng10, Rahul Phadke10, Diana X Bharucha-Goebel7,20, Charlotte Jane Sumner21,22, Mai Thao Bui5,6, Emmanuelle Lacene5,6, Maud Beuvin5,6, Clémence Labasse5,6, Nicolas Dondaine23, Raphael Schneider1,2,3,4,24, Julie Thompson24, Anne Boland25, Jean-François Deleuze25, Emma Matthews10, Aleksandra Nadaj Pakleza26, Caroline A Sewry10, Valérie Biancalana1,2,3,4,23, Susana Quijano-Roy13,14,15,27, Francesco Muntoni10, Michel Fardeau5,6, Carsten G Bönnemann7, Jocelyn Laporte28,29,30,31.
Abstract
Muscle contraction upon nerve stimulation relies on excitation-contraction coupling (ECC) to promote the rapid and generalized release of calcium within myofibers. In skeletal muscle, ECC is performed by the direct coupling of a voltage-gated L-type Ca2+ channel (dihydropyridine receptor; DHPR) located on the T-tubule with a Ca2+ release channel (ryanodine receptor; RYR1) on the sarcoplasmic reticulum (SR) component of the triad. Here, we characterize a novel class of congenital myopathy at the morphological, molecular, and functional levels. We describe a cohort of 11 patients from 7 families presenting with perinatal hypotonia, severe axial and generalized weakness. Ophthalmoplegia is present in four patients. The analysis of muscle biopsies demonstrated a characteristic intermyofibrillar network due to SR dilatation, internal nuclei, and areas of myofibrillar disorganization in some samples. Exome sequencing revealed ten recessive or dominant mutations in CACNA1S (Cav1.1), the pore-forming subunit of DHPR in skeletal muscle. Both recessive and dominant mutations correlated with a consistent phenotype, a decrease in protein level, and with a major impairment of Ca2+ release induced by depolarization in cultured myotubes. While dominant CACNA1S mutations were previously linked to malignant hyperthermia susceptibility or hypokalemic periodic paralysis, our findings strengthen the importance of DHPR for perinatal muscle function in human. These data also highlight CACNA1S and ECC as therapeutic targets for the development of treatments that may be facilitated by the previous knowledge accumulated on DHPR.Entities:
Keywords: Centronuclear myopathy; Congenital myopathy; Core myopathy; DHPR; Excitation–contraction coupling; Myotubular myopathy; Triad
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Year: 2016 PMID: 28012042 DOI: 10.1007/s00401-016-1656-8
Source DB: PubMed Journal: Acta Neuropathol ISSN: 0001-6322 Impact factor: 17.088