Hudes G R, Li W Y, Rockey J H, White P
Department of Medicine, Presbyterian-University of Pennsylvania Medical Center, Philadelphia.
Invest Ophthalmol Vis Sci. 1988 Oct;29(10):1511-6.
Prostaglandin synthesis by bovine retinal pericytes was investigated using high pressure liquid chromatography to separate and identify 3H-labeled prostaglandins released from 3H-arachidonic acid labeled pericyte monolayers. A dominant peak activity corresponding to 6-keto-PGF1 alpha was observed. This peak was eliminated when monolayers were pretreated with cyclooxygenase inhibitors and was augmented when monolayers were stimulated by the calcium ionophore A23187. Suspensions of pericytes and the cell-free media of monolayers incubated with arachidonic acid inhibited adenosine diphosphate-, collagen-, and arachidonic acid-stimulated platelet aggregation in a bioassay for prostacyclin-like activity. This inhibitory activity was unstable at room temperature. Cultures of 7.5 to 10 x 10(5) pericytes (7th passage near-confluence) released nanogram quantities of 6-keto-PGF1 alpha as measured by radioimmunoassay. These results are evidence that prostacyclin is the main prostaglandin synthesized by bovine retinal capillary pericytes in culture. Pericytes may influence the microcirculation via their production and release of this potent vasoactive arachidonic acid metabolite.
利用高压液相色谱法对牛视网膜周细胞的前列腺素合成进行了研究,以分离和鉴定从用³H-花生四烯酸标记的周细胞单层释放的³H标记前列腺素。观察到一个与6-酮-前列环素F1α相对应的主峰活性。当单层细胞用环氧化酶抑制剂预处理时,该峰消失;当单层细胞用钙离子载体A23187刺激时,该峰增强。在一项检测前列环素样活性的生物测定中,周细胞悬液以及与花生四烯酸一起孵育的单层细胞的无细胞培养基抑制了二磷酸腺苷、胶原和花生四烯酸刺激的血小板聚集。这种抑制活性在室温下不稳定。通过放射免疫测定法测得,7.5至10×10⁵个周细胞(第7代接近汇合)的培养物释放出纳克量的6-酮-前列环素F1α。这些结果证明,前列环素是培养的牛视网膜毛细血管周细胞合成的主要前列腺素。周细胞可能通过产生和释放这种强效血管活性花生四烯酸代谢产物来影响微循环。