Creedon D, Tuttle J B
Department of Physiology, University of Virginia Health Sciences Center, Charlottesville 22908.
Hypertension. 1991 Dec;18(6):730-41. doi: 10.1161/01.hyp.18.6.730.
Details of the interdependent, trophic relation between smooth muscle and its neural innervation are not well known despite suggestions that neural influences may contribute significantly to hypertensive and other cardiovascular disease. Vascular smooth muscle is a major target of innervation by neurons of the sympathetic nervous system. Sympathetic neurons depend on a constant supply of the potent neurotrophic peptide nerve growth factor. Nerve growth factor regulates an impressive list of neuronal and perhaps muscle properties, yet its source in vessels and the determinants of its synthesis are not known. We have taken advantage of the cytoarchitecture of the aorta to demonstrate that vascular smooth muscle cells synthesize nerve growth factor. The survival of cultured sympathetic neurons is supported in a nerve growth factor-dependent manner by co-culture with pure rat aortic vascular smooth muscle cells. Furthermore, pure smooth muscle cell cultures contain nerve growth factor-specific messenger RNA. Levels of messenger nucleic acid coding for nerve growth factor in smooth muscle are regulated by contractile agonists (angiotensin II, arginine vasopressin) and the adrenergic agonist phenylephrine. This suggests a link between muscle activity and growth factor production. Secretion of nerve growth factor protein by vascular smooth muscle was measured using a sensitive two-site immunoassay. Secretion is highest during muscle growth. Secretion is elevated by angiotensin II and arginine vasopressin but slightly inhibited by phenylephrine. These results suggest that cultured vascular smooth muscle can serve as a useful model in which to study the cellular regulation of trophic factor synthesis in health and disease.
尽管有观点认为神经影响可能在高血压及其他心血管疾病中起重要作用,但平滑肌与其神经支配之间相互依存的营养关系细节仍不为人所知。血管平滑肌是交感神经系统神经元支配的主要靶点。交感神经元依赖于强效神经营养肽神经生长因子的持续供应。神经生长因子可调节一系列令人瞩目的神经元特性,或许还能调节肌肉特性,但其在血管中的来源及其合成的决定因素尚不清楚。我们利用主动脉的细胞结构来证明血管平滑肌细胞能合成神经生长因子。与纯大鼠主动脉血管平滑肌细胞共培养时,培养的交感神经元的存活以神经生长因子依赖的方式得到支持。此外,纯平滑肌细胞培养物中含有神经生长因子特异性信使核糖核酸。平滑肌中编码神经生长因子的信使核酸水平受收缩激动剂(血管紧张素 II、精氨酸加压素)和肾上腺素能激动剂去氧肾上腺素调节。这表明肌肉活动与生长因子产生之间存在联系。使用灵敏的双位点免疫测定法测量血管平滑肌分泌神经生长因子蛋白的情况。在肌肉生长期间分泌量最高。血管紧张素 II 和精氨酸加压素可提高分泌量,但去氧肾上腺素会使其略有抑制。这些结果表明,培养的血管平滑肌可作为一个有用的模型,用于研究健康和疾病状态下营养因子合成的细胞调节。