Olfert I Mark, Howlett Richard A, Tang Kechun, Dalton Nancy D, Gu Yusu, Peterson Kirk L, Wagner Peter D, Breen Ellen C
Department of Medicine, University of California, San Diego, La Jolla, CA 92093-0623, USA.
J Physiol. 2009 Apr 15;587(Pt 8):1755-67. doi: 10.1113/jphysiol.2008.164384. Epub 2009 Feb 23.
Vascular endothelial growth factor (VEGF) is required for vasculogenesis and angiogenesis during embryonic and early postnatal life. However the organ-specific functional role of VEGF in adult life, particularly in skeletal muscle, is less clear. To explore this issue, we engineered skeletal muscle-targeted VEGF deficient mice (mVEGF-/-) by crossbreeding mice that selectively express Cre recombinase in skeletal muscle under the control of the muscle creatine kinase promoter (MCKcre mice) with mice having a floxed VEGF gene (VEGFLoxP mice). We hypothesized that VEGF is necessary for regulating both cardiac and skeletal muscle capillarity, and that a reduced number of VEGF-dependent muscle capillaries would limit aerobic exercise capacity. In adult mVEGF-/- mice, VEGF protein levels were reduced by 90 and 80% in skeletal muscle (gastrocnemius) and cardiac muscle, respectively, compared to control mice (P < 0.01). This was accompanied by a 48% (P < 0.05) and 39% (P < 0.05) decreases in the capillary-to-fibre ratio and capillary density, respectively, in the gastrocnemius and a 61% decrease in cardiac muscle capillary density (P < 0.05). Hindlimb muscle oxidative (citrate synthase, 21%; beta-HAD, 32%) and glycolytic (PFK, 18%) regulatory enzymes were also increased in mVEGF-/- mice. However, this limited adaptation to reduced muscle VEGF was insufficient to maintain aerobic exercise capacity, and maximal running speed and endurance running capacity were reduced by 34% and 81%, respectively, in mVEGF-/- mice compared to control mice (P < 0.05). Moreover, basal and dobutamine-stimulated cardiac function, measured by transthoracic echocardiography and left ventricular micromanomtery, showed only a minimal reduction of contractility (peak +dP/dt) and relaxation (peak -dP/dt, tau(E)). Collectively these data suggests adequate locomotor muscle capillary number is important for achieving full exercise capacity. Furthermore, VEGF is essential in regulating postnatal muscle capillarity, and that adult mice, deficient in cardiac and skeletal muscle VEGF, exhibit a major intolerance to aerobic exercise.
血管内皮生长因子(VEGF)在胚胎期和出生后早期的血管生成和血管新生过程中是必需的。然而,VEGF在成年期,尤其是在骨骼肌中的器官特异性功能作用尚不清楚。为了探讨这个问题,我们通过将在肌肉肌酸激酶启动子(MCKcre小鼠)控制下在骨骼肌中选择性表达Cre重组酶的小鼠与具有floxed VEGF基因的小鼠(VEGFLoxP小鼠)杂交,构建了骨骼肌靶向VEGF缺陷小鼠(mVEGF-/-)。我们假设VEGF对于调节心肌和骨骼肌的毛细血管密度是必需的,并且依赖VEGF的肌肉毛细血管数量减少会限制有氧运动能力。与对照小鼠相比,成年mVEGF-/-小鼠骨骼肌(腓肠肌)和心肌中的VEGF蛋白水平分别降低了90%和80%(P<0.01)。这伴随着腓肠肌中毛细血管与纤维比率和毛细血管密度分别降低了48%(P<0.05)和39%(P<0.05),以及心肌毛细血管密度降低了61%(P<0.05)。mVEGF-/-小鼠后肢肌肉氧化(柠檬酸合酶,21%;β-羟酰基辅酶A脱氢酶,32%)和糖酵解(磷酸果糖激酶,18%)调节酶也增加。然而,这种对肌肉VEGF减少的有限适应不足以维持有氧运动能力,与对照小鼠相比,mVEGF-/-小鼠的最大跑步速度和耐力跑步能力分别降低了34%和81%(P<0.05)。此外,通过经胸超声心动图和左心室微测法测量的基础和多巴酚丁胺刺激的心脏功能仅显示收缩性(峰值 +dP/dt)和舒张性(峰值 -dP/dt,tau(E))有最小程度的降低。总体而言,这些数据表明足够数量的运动肌肉毛细血管对于实现充分的运动能力很重要。此外,VEGF对于调节出生后肌肉毛细血管密度至关重要,并且成年小鼠缺乏心肌和骨骼肌VEGF时,对有氧运动表现出严重不耐受。