Aging alters gene expression of growth and remodeling factors in human skeletal muscle both at rest and in response to acute resistance exercise.

TitleAging alters gene expression of growth and remodeling factors in human skeletal muscle both at rest and in response to acute resistance exercise.
Publication TypeJournal Article
Year of Publication2008
AuthorsDennis RA, Przybyla B, Gurley C, Kortebein PM, Simpson P, Sullivan DH, Peterson CA
JournalPhysiol Genomics
Volume32
Issue3
Pagination393-400
Date Published2008 Feb 19
ISSN1531-2267
KeywordsActins, Adult, Aged, Aging, Ciliary Neurotrophic Factor, Gene Expression Profiling, Gene Expression Regulation, Humans, Insulin-Like Growth Factor Binding Protein 5, Insulin-Like Growth Factor I, Intercellular Signaling Peptides and Proteins, Male, Matrix Metalloproteinase 2, Muscle Proteins, Muscle, Skeletal, Myostatin, Rest, Reverse Transcriptase Polymerase Chain Reaction, RNA, Messenger, Tissue Inhibitor of Metalloproteinase-1, Transforming Growth Factor beta, Weight Lifting
Abstract

The purpose of this investigation was to compare expression of genes that function in inflammation and stress, cell structure and signaling, or remodeling and growth in skeletal muscle of young (32 +/- 7 yr, n = 15) and elderly (72 +/- 5 yr, n = 16) healthy subjects before and after a bout of resistance leg exercises. A real-time RT-PCR method was used to screen 100 transcripts in v. lateralis biopsies obtained before and 72 h postexercise. The screen identified 15 candidates for differential expression due to aging and/or exercise that were measured quantitatively. The median levels of four mRNAs (insulin-like growth factor-1 and its binding protein IGFBP5, ciliary neurotrophic factor, and the metallopeptidase MMP2) were significantly affected by aging and were greater (1.6- to 2.3-fold, P

DOI10.1152/physiolgenomics.00191.2007
Alternate JournalPhysiol. Genomics
PubMed ID18073271
PubMed Central IDPMC6581202
Grant ListM01-RR14288 / RR / NCRR NIH HHS / United States
P01 AG012411 / AG / NIA NIH HHS / United States
P20 RR-16460 / RR / NCRR NIH HHS / United States
P20 RR016460 / RR / NCRR NIH HHS / United States
M01 RR014288 / RR / NCRR NIH HHS / United States
AG012411 / AG / NIA NIH HHS / United States