Transcriptional reprogramming and ultrastructure during atrophy and recovery of mouse soleus muscle

• Published in: Physiological genomics 2004-12, Vol.20 (1), p.97-107
• Main Authors: Dapp, Christoph, Schmutz, Silvia, Hoppeler, Hans, Fluck, Martin
• Format: Article
• Language: English
• Subjects: Animals; Atrophy; DNA, Complementary - metabolism; Female; Gene Expression Regulation; Glycolysis; Hindlimb Suspension; Mice; Mice, Inbred C57BL; Microscopy, Electron; Muscle, Skeletal - metabolism; Muscle, Skeletal - pathology; Muscle, Skeletal - ultrastructure; Muscles - metabolism; Muscular Atrophy; Myocardium - ultrastructure; Nucleic Acid Hybridization; Oligonucleotide Array Sequence Analysis; Oxygen - metabolism; Phenotype; Rats; Reverse Transcriptase Polymerase Chain Reaction; RNA - metabolism; RNA, Messenger - metabolism; Stress, Mechanical; Transcription, Genetic; Weightlessness
• ISSN: 1094-8341; 1531-2267
• DOI: 10.1152/physiolgenomics.00100.2004

Institute of Anatomy, University of Bern, Bern, Switzerland This study investigated the use of the hindlimb suspension (HS) and reloading model of mice for the mapping of ultrastructural and gene expressional alterations underlying load-dependent muscular adaptations. Mice were hindlimb suspended for 7 days or kept as controls ( n = 12). Soleus muscles were harvested after HS (HS7, n = 23) or after resuming ambulatory cage activity (reloading) for either 1 day (R1, n = 13) or 7 days (R7, n = 9). Using electron microscopy, a reduction in mean fiber area (–37%) and in capillary-to-fiber ratio (from 1.83 to 1.42) was found for HS7. Subsequent reloading caused an increase in interstitial cells (+96%) and in total capillary length (+57%), whereas mean fiber area and capillary-to-fiber ratio did not significantly change compared with HS. Total RNA in the soleus muscle was altered with both HS (–63%) and reloading (+108% in R7 compared with control). This is seen as an important adaptive mechanism. Gene expression alterations were assessed by a muscle-specific low-density cDNA microarray. The transcriptional adjustments indicate an early increase of myogenic factors during reloading together with an overshoot of contractile (MyHC I and IIa) and metabolic (glycolytic and oxidative) mRNA amounts and suggest mechano-sensitivity of factors keeping the sarcomeres in register (desmin, titin, integrin-ß1). Important differences to published data from former rat studies were found with the mouse HS model for contractile and glycolytic enzyme expression. These species-specific differences need to be considered when transgenic mice are used for the elucidation of monogenetic factors in mechano-dependent muscle plasticity. unloading; mechanical loading; simulated microgravity; gene expression; rat