Ganz P, Davies P F, Leopold J A, Gimbrone M A, Alexander R W
Proc Natl Acad Sci U S A. 1986 May;83(10):3552-6. doi: 10.1073/pnas.83.10.3552.
In intact blood vessels, many vasodilators act by stimulating the release from endothelium of factor(s) that relax vascular smooth muscle and stimulate increases in cGMP. To investigate how endothelium regulates cGMP production in vascular smooth muscle, bovine aortic endothelial cells and rat aortic smooth muscle cells were cultured both separately and together in cocultures for 48 hr. Nitroprusside (1 mM) increased intracellular cGMP concentration 30-fold in smooth muscle cells (from a basal level of 103 +/- 54 fmol/mg of cell protein to 2920 +/- 1800 fmol/mg) but only 2-fold in endothelial cells (from 41 +/- 7 fmol/mg to 93 +/- 23 fmol/mg). When endothelial and smooth muscle cells were cocultured as a mixed cell population (1:1 cell ratio), both basal and nitroprusside-stimulated cGMP levels were significantly increased (550 +/- 250 and 13,240 +/- 9950 fmol/mg of total cell protein, respectively). The calcium ionophore A23187 (10 microM) caused no increase in cGMP concentration in either cell type cultured alone but produced a 6-fold increase in cocultures. Neither aspirin nor 5,8,11,14-icosatetraynoic acid influenced these results. No changes in cAMP levels were detected. Using cocultures in which one cell type was grown on microcarrier beads, we have shown that cGMP increased only in vascular smooth muscle cells and was not dependent upon the formation of junctions between endothelium and smooth muscle cells. In long-term (48-hr) mixed-cell cocultures, but not in short-term microcarrier cocultures, amplification of the nitroprusside-induced increase in cGMP was observed. These results show that responses associated with endothelium-dependent relaxation can be reconstituted in cultured endothelial and vascular smooth muscle cells and that endothelium generates a humoral factor(s) that stimulates accumulation of smooth muscle cGMP and has a longer-term effect that amplifies guanylate cyclase stimulation by nitroprusside, a drug acting directly upon smooth muscle to stimulate formation of the cyclic nucleotide. Cultured cells provide a valuable model system for the study of endothelium-vascular smooth muscle interactions.
在完整的血管中,许多血管舒张剂通过刺激内皮细胞释放某种因子来发挥作用,这些因子可使血管平滑肌松弛并刺激环鸟苷酸(cGMP)生成增加。为了研究内皮细胞如何调节血管平滑肌中的cGMP生成,分别培养了牛主动脉内皮细胞和大鼠主动脉平滑肌细胞,并将它们共同培养48小时。硝普钠(1 mM)使平滑肌细胞内的cGMP浓度增加了30倍(从基础水平的103±54 fmol/mg细胞蛋白增加到2920±1800 fmol/mg),但在内皮细胞中仅增加了2倍(从41±7 fmol/mg增加到93±23 fmol/mg)。当内皮细胞和平滑肌细胞以混合细胞群体(1:1细胞比例)共同培养时,基础cGMP水平和硝普钠刺激后的cGMP水平均显著增加(分别为550±250和13240±9950 fmol/mg总细胞蛋白)。钙离子载体A23187(10 μM)在单独培养的任何一种细胞类型中均未引起cGMP浓度升高,但在共同培养中使其增加了6倍。阿司匹林和5,8,11,14-二十碳四炔酸均未影响这些结果。未检测到环磷酸腺苷(cAMP)水平的变化。使用一种细胞类型生长在微载体珠上的共同培养体系,我们发现cGMP仅在血管平滑肌细胞中增加,且不依赖于内皮细胞和平滑肌细胞之间连接的形成。在长期(48小时)混合细胞共同培养中,但在短期微载体共同培养中未观察到硝普钠诱导的cGMP增加的放大效应。这些结果表明,与内皮依赖性舒张相关的反应可以在培养的内皮细胞和血管平滑肌细胞中重建,并且内皮细胞产生一种体液因子,该因子刺激平滑肌cGMP的积累,并具有长期效应,可放大硝普钠对鸟苷酸环化酶的刺激作用,硝普钠是一种直接作用于平滑肌以刺激环核苷酸形成的药物。培养的细胞为研究内皮细胞与血管平滑肌相互作用提供了一个有价值的模型系统。