Lopes Francis da Silva, Carvalho Robson Francisco, Campos Gerson Eduardo Rocha, Sugizaki Mario Matheus, Padovani Carlos Roberto, Nogueira Célia Regina, Cicogna Antonio Carlos, Pai-Silva Maeli Dal
Departamentos de Biologia Celular e Anatomia, UNICAMP, Campinas, Brasil.
Int J Exp Pathol. 2008 Jun;89(3):216-22. doi: 10.1111/j.1365-2613.2008.00587.x.
Diaphragm myopathy has been described in patients with heart failure (HF), with alterations in myosin heavy chains (MHC) expression. The pathways that regulate MHC expression during HF have not been described, and myogenic regulatory factors (MRFs) may be involved. The purpose of this investigation was to determine MRF mRNA expression levels in the diaphragm. Diaphragm muscle from both HF and control Wistar rats was studied when overt HF had developed, 22 days after monocrotaline administration. MyoD, myogenin and MRF4 gene expression were determined by RT-PCR and MHC isoforms by polyacrylamide gel electrophoresis. Heart failure animals presented decreased MHC IIa/IIx protein isoform and MyoD gene expression, without altering MHC I, IIb, myogenin and MRF4. Our results show that in HF, MyoD is selectively down-regulated, which might be associated with alterations in MHC IIa/IIx content. These changes are likely to contribute to the diaphragm myopathy caused by HF.
心力衰竭(HF)患者中已发现膈肌肌病,伴有肌球蛋白重链(MHC)表达改变。HF期间调节MHC表达的途径尚未明确,生肌调节因子(MRF)可能参与其中。本研究的目的是确定膈肌中MRF mRNA的表达水平。在给予野百合碱22天后,当明显的HF形成时,对HF和对照Wistar大鼠的膈肌进行研究。通过逆转录聚合酶链反应(RT-PCR)测定MyoD、肌细胞生成素和MRF4基因的表达,并通过聚丙烯酰胺凝胶电泳测定MHC亚型。心力衰竭动物的MHC IIa/IIx蛋白亚型和MyoD基因表达降低,而MHC I、IIb、肌细胞生成素和MRF4未发生改变。我们的结果表明,在HF中,MyoD被选择性下调,这可能与MHC IIa/IIx含量的改变有关。这些变化可能导致HF引起的膈肌肌病。