Marceau F, Tremblay B
Life Sci. 1986 Dec 15;39(24):2351-8. doi: 10.1016/0024-3205(86)90666-1.
Bradykinin (BK) and its fragment des-Arg9-BK failed to stimulate thymidine incorporation in all but one observed fibroblast cultures derived from human amniotic fluid or rabbit dermis. The rabbit dermis fibroblast line designated R51 acquired the capacity to increase its DNA synthesis in response to kinins after several weeks in culture. It was more sensitive to des-Arg9-BK than to BK and the effect of both peptides was antagonized by the analog Leu8, des-Arg9-BK; these features are shared with certain smooth muscle preparations responsive to kinins such as the rabbit aorta. Recently isolated rabbit dermis or human amniotic fibroblasts could not be made responsive to kinins by pre-incubating them with bacterial lipopolysaccharide. The line R51 released more PGE2 than baseline when stimulated with BK or des-Arg9-BK at low concentrations; it was also doubling faster than recently isolated cells of similar origin.
除了从人羊水或兔真皮中获得的一种成纤维细胞培养物外,缓激肽(BK)及其片段去精氨酸9 - 缓激肽(des-Arg9-BK)均未能刺激胸苷掺入。在培养数周后,名为R51的兔真皮成纤维细胞系获得了响应激肽增加其DNA合成的能力。它对去精氨酸9 - 缓激肽的敏感性高于缓激肽,并且两种肽的作用都被类似物亮氨酸8、去精氨酸9 - 缓激肽所拮抗;这些特征与某些对激肽有反应的平滑肌制剂(如兔主动脉)相同。最近分离的兔真皮或人羊膜成纤维细胞,用细菌脂多糖预孵育也不能使其对激肽产生反应。当用低浓度的缓激肽或去精氨酸9 - 缓激肽刺激时,R51细胞系释放的前列腺素E2比基线水平更多;它的增殖速度也比最近分离的相似来源细胞快一倍。