| Literature DB >> 26719336 |
Jeff P Gorski1, Nichole T Huffman2, Julian Vallejo3, Leticia Brotto3, Sridar V Chittur4, Anne Breggia5, Amber Stern6, Jian Huang3, Chenglin Mo3, Nabil G Seidah7, Lynda Bonewald2, Marco Brotto3.
Abstract
Conditional deletion of Mbtps1 (cKO) protease in bone osteocytes leads to an age-related increase in mass (12%) and in contractile force (30%) in adult slow twitch soleus muscles (SOL) with no effect on fast twitch extensor digitorum longus muscles. Surprisingly, bone from 10-12-month-old cKO animals was indistinguishable from controls in size, density, and morphology except for a 25% increase in stiffness. cKO SOL exhibited increased expression of Pax7, Myog, Myod1, Notch, and Myh3 and 6-fold more centralized nuclei, characteristics of postnatal regenerating muscle, but only in type I myosin heavy chain-expressing cells. Increased expression of gene pathways mediating EGF receptor signaling, circadian exercise, striated muscle contraction, and lipid and carbohydrate oxidative metabolism were also observed in cKO SOL. This muscle phenotype was not observed in 3-month-old mice. Although Mbtps1 mRNA and protein expression was reduced in cKO bone osteocytes, no differences in Mbtps1 or cre recombinase expression were observed in cKO SOL, explaining this age-related phenotype. Understanding bone-muscle cross-talk may provide a fresh and novel approach to prevention and treatment of age-related muscle loss.Entities:
Keywords: DMP1; MBTPS1; bone; cell signaling; centralized nuclei; cross-talk; gene knock-out; osteocyte; regeneration; skeletal muscle
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Year: 2015 PMID: 26719336 PMCID: PMC4813460 DOI: 10.1074/jbc.M115.686626
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157