Wagatsuma A, Tamaki H, Ogita F
Department of Physiological Sciences, National Institute of Fitness and Sports, Shiromizu-cho 1, Kanoya, Kagoshima 891-2393, Japan.
Exp Physiol. 2005 May;90(3):403-9. doi: 10.1113/expphysiol.2004.029769. Epub 2005 Feb 11.
Capillary supply of skeletal muscle decreases during denervation. To gain insight into the regulation of this process, we investigated capillary supply and gene expression of angiogenesis-related factors in mouse gastrocnemius muscle following denervation for 4 months. Frozen transverse sections were stained for alkaline phosphatase to detect endogenous enzyme in the capillary endothelium. The mRNA for angiogenesis-related factors, including hypoxia inducible factor-1alpha (HIF-1alpha), vascular endothelial growth factor (VEGF), kinase insert domain-containing receptor/fetal liver kinase-1 (KDR/Flk-1), fms-like tyrosine kinase (Flt-1), angiopoietin-1 and tyrosine kinase with Ig and epidermal growth factor(EGF) homology domain 2 (Tie-2), was analysed using a semi-quantitative reverse transcriptase-polymerase chain reaction (RT-PCR). The fibre cross-sectional area after denervation was about 20% of the control value, and the capillary to fibre ratio was significantly lower in denervated than in control muscles. The number of capillaries around each fibre also decreased to about 40% of the control value. These observations suggest that muscle capillarity decreases in response to chronic denervation. RT-PCR analysis showed that the expression of VEGF mRNA was lower in denervated than in control muscles, while the expression of HIF-1alpha mRNA remained unchanged. The expression levels of the KDR/Flk-1 and Flt-1 genes were decreased in the denervated muscle. The expression levels of angiopoietin-1 but not Tie-2 genes were decreased in the denervated muscle. These findings indicate that reduction in the expression of mRNAs in the VEGF/KDR/Flk-1 and Flt-1 as well as angiopoietin-1/Tie-2 signal pathways might be one of the reasons for the capillary regression during chronic denervation.
去神经支配期间骨骼肌的毛细血管供应减少。为深入了解这一过程的调节机制,我们研究了去神经支配4个月后小鼠腓肠肌的毛细血管供应及血管生成相关因子的基因表达。将冰冻横切片用碱性磷酸酶染色,以检测毛细血管内皮中的内源性酶。使用半定量逆转录聚合酶链反应(RT-PCR)分析血管生成相关因子的mRNA,包括缺氧诱导因子-1α(HIF-1α)、血管内皮生长因子(VEGF)、含激酶插入结构域受体/胎儿肝激酶-1(KDR/Flk-1)、fms样酪氨酸激酶(Flt-1)、血管生成素-1以及具有免疫球蛋白和表皮生长因子(EGF)同源结构域2的酪氨酸激酶(Tie-2)。去神经支配后的肌纤维横截面积约为对照值的20%,且去神经支配的肌肉中毛细血管与肌纤维的比例显著低于对照肌肉。每根肌纤维周围的毛细血管数量也减少至对照值的约40%。这些观察结果表明,慢性去神经支配会导致肌肉毛细血管密度降低。RT-PCR分析显示,去神经支配的肌肉中VEGF mRNA的表达低于对照肌肉,而HIF-1α mRNA的表达保持不变。去神经支配的肌肉中KDR/Flk-1和Flt-1基因的表达水平降低。去神经支配的肌肉中血管生成素-1基因的表达水平降低,但Tie-2基因的表达水平未降低。这些发现表明,VEGF/KDR/Flk-1和Flt-1以及血管生成素-1/Tie-2信号通路中mRNA表达的降低可能是慢性去神经支配期间毛细血管退化的原因之一。