Deletion of Mbtps1 (Pcsk8, S1p, Ski-1) Gene in Osteocytes Stimulates Soleus Muscle Regeneration and Increased Size and Contractile Force with Age
Male
Mice, Knockout
0301 basic medicine
Sarcopenia
Gene Expression Profiling
Musculoskeletal Development
Serine Endopeptidases
Gene Expression Regulation, Developmental
Muscle Development
Osteocytes
03 medical and health sciences
Muscle Fibers, Slow-Twitch
Myogenic Regulatory Factors
Animals
Muscle Strength
Proprotein Convertases
RNA, Messenger
Energy Metabolism
Muscle, Skeletal
Crosses, Genetic
Muscle Contraction
Transcription Factors
DOI:
10.1074/jbc.m115.686626
Publication Date:
2015-12-31T03:43:34Z
AUTHORS (12)
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.
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