Hansen-Smith F, Egginton S, Zhou A L, Hudlicka O
Department of Biological Sciences and Center for Biomedical Research, Oakland University, Rochester, Michigan 48309-4401, USA.
Microvasc Res. 2001 Jul;62(1):1-14. doi: 10.1006/mvre.2001.2308.
Arteriolar growth accompanying capillary angiogenesis has been linked with hemodynamic factors resulting from increased blood flow. Here we describe the growth of arterioles occurring in rat skeletal muscles stretched by an overload due to the removal of agonist muscles, where blood flow was not increased, and we provide morphological evidence for the type of cells involved in this growth. Rat extensor digitorum longus (EDL) and extensor hallucis proprius (EHP) were overloaded by unilateral extirpation of their agonist, tibialis anterior. EDL muscles were taken for immunohistochemistry in cryostat sections to mark endothelial cells (Griffonia simplicifolia I, GSI lectin), smooth muscle cells and pericytes (alpha smooth muscle actin, alphaSMA), and "mature" arterioles (smooth muscle myosin heavy chains). EHP muscles were used for corresponding evaluation by confocal and electron microscopy. The number of capillaries surrounding muscle fibers was not significantly different after 1 week of stretch but was higher after 2 weeks (5.15 +/- 0.2 vs 4.3 +/- 0.2 in controls, P < 0.05). Similarly, capillary density (CD) and capillary/fiber ratio (C/F) gradually increased (CD 778 +/- 86 at 2 weeks vs 593 +/- 35 mm(-2) in controls, C/F 2.07 +/- 0.13 vs 1.38 +/- 0.06, respectively). In contrast, the number of alphaSMA-positive vessels around fibers increased after 1 week (2.16 +/- 0.09 vs 0.25 +/- 0.02 in controls) and was lower after 2 weeks (1.42 +/- 0.24, P < 0.05, vs 1 week). Arteriolar density was higher at 1 (110.9 +/- 7.5 mm(-2)) and 2 weeks (70.7 +/- 12.1) with respect to controls (31.0 +/- 1.6 mm(-2)). The increased density was greater in alphaSMA-positive vessels <10 microm in diameter (controls 18.0 +/- 1.04, 1 week 77.2 +/- 4.5, 2 wk 42.2 +/- 9.0 mm(-2)) than in vessels >10 microm (13.0 +/- 0.8, 33.7 +/- 4.0, 29.5 +/- 4.7 mm(-2)). Electron microscopy showed "activated" (TEM fine structure) and proliferating (immunogold labeling for BrdU) fibroblasts in the vicinity of capillaries, some of which were embedded in the capillary basement membrane, consistent with a transformation into pericytes and possibly later smooth muscle cells. Confocal microscopy indicated that some mesenchymal cells became GSI positive and formed extended processes which contacted capillaries via tapered endings. Growth of arterioles in stretched muscles appears to involve proliferation of fibroblasts, which may migrate toward capillaries and precedes any apparent increase in capillarization.
伴随毛细血管生成的小动脉生长与血流量增加所产生的血流动力学因素有关。在此,我们描述了因去除协同肌导致过载而拉伸的大鼠骨骼肌中发生的小动脉生长情况,这种情况下血流量并未增加,并且我们提供了参与这种生长的细胞类型的形态学证据。通过单侧切除大鼠趾长伸肌(EDL)和拇长伸肌(EHP)的协同肌胫骨前肌,使其产生过载。取EDL肌肉进行冰冻切片免疫组织化学,以标记内皮细胞(简氏相思子凝集素I,GSI凝集素)、平滑肌细胞和周细胞(α平滑肌肌动蛋白,αSMA)以及“成熟”小动脉(平滑肌肌球蛋白重链)。用EHP肌肉通过共聚焦显微镜和电子显微镜进行相应评估。拉伸1周后,围绕肌纤维的毛细血管数量与对照组相比无显著差异,但在2周后更高(对照组为4.3±0.2,拉伸组为5.15±0.2,P<0.05)。同样,毛细血管密度(CD)和毛细血管/纤维比(C/F)逐渐增加(2周时CD为778±86,对照组为593±35 mm⁻²;C/F分别为2.07±0.13和1.38±0.06)。相比之下,纤维周围αSMA阳性血管数量在1周后增加(对照组为0.25±0.02,拉伸组为2.16±0.09),在2周后减少(1.42±0.24,与1周相比P<0.05,对照组为1.38±0.06)。与对照组(31.0±1.6 mm⁻²)相比,小动脉密度在1周(110.9±7.5 mm⁻²)和2周(70.7±12.1)时更高。直径<10μm的αSMA阳性血管密度增加幅度(对照组为18.0±1.04,1周为77.2±4.5,2周为42.2±9.0 mm⁻²)大于直径>10μm的血管(分别为13.0±0.8,33.7±4.0,29.5±4.7 mm⁻²)。电子显微镜显示在毛细血管附近有“活化”(透射电镜精细结构)和增殖(BrdU免疫金标记)的成纤维细胞,其中一些嵌入毛细血管基底膜,这与向周细胞进而可能向平滑肌细胞的转变一致。共聚焦显微镜表明一些间充质细胞变为GSI阳性,并形成延伸的突起,通过逐渐变细的末端与毛细血管接触。拉伸肌肉中小动脉的生长似乎涉及成纤维细胞的增殖,成纤维细胞可能向毛细血管迁移,并先于毛细血管化的任何明显增加。