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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

alpha-Calcitonin gene-related peptide inhibits autophagy and calpain systems and maintains the stability of neuromuscular junction in denervated muscles

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Author(s):
Machado, Juliano [1, 2, 3, 4] ; Silveira, Wilian A. [1, 5] ; Goncalves, Dawit A. [1, 2, 6] ; Schavinski, Aline Zanatta [1] ; Khan, Muzamil M. [7, 8, 9] ; Zanon, Neusa M. [1] ; Diaz, Mauricio Berriel [3, 4] ; Rudolf, Ruediger [7, 8, 9] ; Kettelhut, Isis C. [2] ; Navegantes, Luiz C. [1]
Total Authors: 10
Affiliation:
[1] Univ Sao Paulo, Ribeirao Preto Med Sch, Dept Physiol, BR-14049900 Ribeirao Preto, SP - Brazil
[2] Univ Sao Paulo, Ribeirao Preto Med Sch, Dept Biochem Immunol, Ribeirao Preto, SP - Brazil
[3] Helmholtz Ctr Munich, IDC, D-85764 Neuherberg - Germany
[4] Heidelberg Univ Hosp, Joint Heidelberg IDC Translat Diabet Program, Inner Med 1, D-69120 Heidelberg - Germany
[5] Univ Fed Triangulo Mineiro, Inst Biol & Nat Sci, Uberaba, MG - Brazil
[6] Fed Univ Minas Gerais UFMG, Exercise Physiol Lab, Sch Phys Educ Physiotherapy & Occupat Therapy, Belo Horizonte, MG - Brazil
[7] Univ Appl Sci Mannheim, Inst Mol & Cell Biol, Mannheim - Germany
[8] Heidelberg Univ, Inst Med Technol, Mannheim - Germany
[9] Univ Appl Sci Mannheim, Mannheim - Germany
Total Affiliations: 9
Document type: Journal article
Source: MOLECULAR METABOLISM; v. 28, p. 91-106, OCT 2019.
Web of Science Citations: 0
Abstract

Objective: Although it is well established that a-calcitonin gene-related peptide (CGRP) stabilizes muscle-type cholinergic receptors nicotinic subunits (AChR), the underlying mechanism by which this neuropeptide regulates muscle protein metabolism and neuromuscular junction (NMJ) morphology is unclear. Methods: To elucidate the mechanisms how CGRP controls NMJ stability in denervated mice skeletal muscles, we carried out physiological, pharmacological, and molecular analyses of atrophic muscles induced by sciatic nerve transection. Results: Here, we report that CGRP treatment in vivo abrogated the deleterious effects on NMJ upon denervation (DEN), an effect that was associated with suppression of skeletal muscle proteolysis, but not stimulation of protein synthesis. CGRP also blocked the DEN-induced increase in endocytic AChR vesicles and the elevation of autophagosomes per NMJ area. The treatment of denervated animals with rapamycin blocked the stimulatory effects of CGRP on mTORC1 and its inhibitory actions on autophagic flux and NMJ degeneration. Furthermore, CGRP inhibited the DEN-induced hyperactivation of Ca2+-dependent proteolysis, a degradative system that has been shown to destabilize NMJ. Consistently, calpain was found to be activated by cholinergic stimulation in myotubes leading to the dispersal of AChR clusters, an effect that was abolished by CGRP. Conclusion: Taken together, these data suggest that the inhibitory effect of CGRP on autophagy and calpain may represent an important mechanism for the preservation of synapse morphology when degradative machinery is exacerbated upon denervation conditions. (C) 2019 The Authors. Published by Elsevier GmbH. (AU)

FAPESP's process: 09/54014-7 - Acquisition of a biophotonic imaging system and a multiphoton microscopy system for in vivo imaging
Grantee:Enilza Maria Espreafico
Support type: Multi-user Equipment Program
FAPESP's process: 11/11003-5 - The role of calcitonin-gene related peptide (CGRP) in the control of protein metabolism in normal and denervated rat skeletal muscle
Grantee:Luiz Carlos Carvalho Navegantes
Support type: Regular Research Grants
FAPESP's process: 12/24524-6 - Control of muscle mass by cAMP signaling pathway
Grantee:Isis Do Carmo Kettelhut
Support type: Research Projects - Thematic Grants
FAPESP's process: 18/10089-2 - Neural, hormonal and nutritional control of autophagy
Grantee:Isis Do Carmo Kettelhut
Support type: Research Projects - Thematic Grants
FAPESP's process: 12/18861-0 - FOXO HYPERACETYLATION AS A MECHANISM OF SUPPRESSION OF ATROPHY GENE PROGRAM INDUCED BY BETA2-ADRENERGIC SIGNALING IN RODENT SKELETAL MUSCLE
Grantee:Dawit Albieiro Pinheiro Gonçalves
Support type: Scholarships in Brazil - Post-Doctorate