Alterations in gene expression in hamster diaphragm after emphysema and lung volume reduction surgery

The authors have demonstrated previously that emphysema and lung volume reduction surgery (LVRS) resulted in a significant shift of type IIx/b to type IIa fibres in the diaphragm of hamsters with elastase-induced emphysema. To explore the mechanisms leading to this fibre switching, the mRNA expression of the myogenic regulatory factors, the inhibitors of DNA binding proteins (Id-proteins) and insulin-like growth factor-I were examined. Ribonucleic acid was extracted from the diaphragm of control, emphysematous, emphysematous and sham operated and LVRS hamsters and subjected to reverse transcriptase polymerase chain reaction. Compared to control, the ratio MyoD to myogenin declined with emphysema, sham and even more after LVRS, due to a decrease in MyoD mRNA and an increase in myogenin mRNA. Similarly, compared to control, Id-1 protein mRNA levels decreased significantly in sham and even more in LVRS. Id-2 protein mRNA levels decreased in all groups, but reached statistical significance in LVRS only, compared to control. In conclusion: 1) the reduced MyoD/myogenin ratio may be the mechanism of the shift to a slower fibre type, 2) the decreased MyoD/myogenin ratio in lung volume reduction surgery animals suggests that lung volume reduction surgery enhances rather than decreases the load placed on the diaphragm and 3) the observed down-regulation of the inhibiting factors may facilitate the diaphragm adaptation to overload.

[1]  G. Snider,et al.  Animal models of emphysema. , 1986, The American review of respiratory disease.

[2]  D. Lomas Lung volume reduction surgery: where are we now? , 2004, Chronic respiratory disease.

[3]  M. Rudnicki,et al.  bHLH transcription factor MyoD affects myosin heavy chain expression pattern in a muscle-specific fashion. , 2001, American journal of physiology. Cell physiology.

[4]  M. Decramer,et al.  Lung volume reduction surgery does not improve diaphragmatic contractile properties or atrophy in hamsters with elastase-induced emphysema. , 2000, American journal of respiratory and critical care medicine.

[5]  M. Fournier,et al.  Functional, cellular, and biochemical adaptations to elastase-induced emphysema in hamster medial scalene. , 2000, Journal of applied physiology.

[6]  O. H. Lowry,et al.  Myogenin Induces a Shift of Enzyme Activity from Glycolytic to Oxidative Metabolism in Muscles of Transgenic Mice , 1999, The Journal of cell biology.

[7]  P. Mozdziak,et al.  Myogenin, MyoD, and myosin heavy chain isoform expression following hindlimb suspension. , 1999, Aviation, space, and environmental medicine.

[8]  M. Fournier,et al.  Respiratory work in elastase treated hamsters. , 1998, Respiration physiology.

[9]  C. Peterson,et al.  Early changes in muscle fiber size and gene expression in response to spinal cord transection and exercise. , 1998, American journal of physiology. Cell physiology.

[10]  G. Adams,et al.  Localized infusion of IGF-I results in skeletal muscle hypertrophy in rats. , 1998, Journal of applied physiology.

[11]  S. Schiaffino,et al.  Myosin heavy chain gene expression changes in the diaphragm of patients with chronic lung hyperinflation. , 1998, The American journal of physiology.

[12]  L. Kaiser,et al.  Cellular adaptations in the diaphragm in chronic obstructive pulmonary disease. , 1997, The New England journal of medicine.

[13]  E. Prochownik,et al.  Differential Interactions of Id Proteins with Basic-Helix-Loop-Helix Transcription Factors* , 1997, The Journal of Biological Chemistry.

[14]  D. Pette,et al.  Quantification of MyoD, myogenin, MRF4 and Id-1 by reverse-transcriptase polymerase chain reaction in rat muscles--effects of hypothyroidism and chronic low-frequency stimulation. , 1997, European journal of biochemistry.

[15]  H. Simpson,et al.  Changes in muscle fibre type, muscle mass and IGF‐I gene expression in rabbit skeletal muscle subjected to stretch , 1997, Journal of anatomy.

[16]  L. Henderson,et al.  Adaptation of nicotinic acetylcholine receptor, myogenin, and MRF4 gene expression to long-term muscle denervation , 1995, The Journal of cell biology.

[17]  K. Gundersen,et al.  Id-1 as a possible transcriptional mediator of muscle disuse atrophy. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[18]  S. Badylak,et al.  Differential expression of muscle regulatory factor genes in normal and denervated adult rat hindlimb muscles , 1993, Developmental dynamics : an official publication of the American Association of Anatomists.

[19]  S. Tapscott,et al.  Selective accumulation of MyoD and myogenin mRNAs in fast and slow adult skeletal muscle is controlled by innervation and hormones. , 1993, Development.

[20]  E. Olson,et al.  Helix-loop-helix proteins as regulators of muscle-specific transcription. , 1993, The Journal of biological chemistry.

[21]  B. Kirschbaum,et al.  Antagonistic effects of chronic low frequency stimulation and thyroid hormone on myosin expression in rat fast-twitch muscle. , 1990, The Journal of biological chemistry.

[22]  P. Bechtel,et al.  Activation of insulin-like growth factor gene expression during work-induced skeletal muscle growth. , 1990, The American journal of physiology.

[23]  Harold Weintraub,et al.  The protein Id: A negative regulator of helix-loop-helix DNA binding proteins , 1990, Cell.

[24]  Y. Jan,et al.  Interactions between heterologous helix-loop-helix proteins generate complexes that bind specifically to a common DNA sequence , 1989, Cell.

[25]  W. Rutter,et al.  Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. , 1979, Biochemistry.

[26]  D. Leith,et al.  Respiratory mechanics in normal hamsters. , 1976, Journal of applied physiology.

[27]  E. Russi,et al.  Lung volume reduction surgery: a survey on the European experience. , 2000, Chest.

[28]  M. Decramer,et al.  Acute treatment with corticosteroids decreases IGF-1 and IGF-2 expression in the rat diaphragm and gastrocnemius. , 1999, American journal of respiratory and critical care medicine.

[29]  P. Loughna,et al.  Regulation of insulin-like growth factor 1 gene expression in skeletal muscle. , 1992, Symposia of the Society for Experimental Biology.

[30]  G. Snider,et al.  Animal models of emphysema. , 1978, The American review of respiratory disease.