Amat M, Díaz C, Vila L
Santa Creu i Sant Pau Hospital, Barcelona, Spain.
Arthritis Rheum. 1998 Sep;41(9):1645-51. doi: 10.1002/1529-0131(199809)41:9<1645::AID-ART16>3.0.CO;2-Z.
To investigate the cooperation of chondrocytes and polymorphonuclear cells (PMN) in the biosynthesis of leukotrienes (LT).
PMN, resting and interleukin-1beta-stimulated cultured human chondrocytes, and mixtures of both cell types were incubated with A23187 and/or 14C-arachidonic acid (14C-AA). To explore the presence of LTC4 synthase and LTA4 hydrolase, the chondrocytes were incubated with authentic LTA4. Eicosanoids were analyzed using high performance liquid chromatography techniques.
Chondrocytes formed only prostaglandin E2 and minor amounts of 15-HETE and 11-HETE, the production of all of which was inhibited by 1 microM indomethacin. Incubation of PMN and chondrocytes produced more LTC4 from endogenous and exogenous AA, and more LTB4 from endogenous AA, than incubation of PMN alone, which was consistent with the presence of LTC4 synthase and LTA4 hydrolase activities in chondrocytes. Chondrocytes also slightly increased the level of PMN production of all 5-lipoxygenase (5-LO)-derived products from endogenous AA.
Human chondrocytes form eicosanoids from AA only by the cyclooxygenase pathway. Chondrocytes cooperate in the transcellular biosynthesis of LT since they possess LTA4 hydrolase and LTC4 synthase activities and increase metabolism by the 5-LO pathway in PMN.
研究软骨细胞与多形核细胞(PMN)在白三烯(LT)生物合成中的协作作用。
将PMN、静息及经白细胞介素-1β刺激培养的人软骨细胞,以及这两种细胞类型的混合物与A23187和/或14C-花生四烯酸(14C-AA)一起孵育。为探究白三烯C4合酶和白三烯A4水解酶的存在情况,将软骨细胞与真实的白三烯A4一起孵育。使用高效液相色谱技术分析类花生酸。
软骨细胞仅生成前列腺素E2以及少量的15-羟基二十碳四烯酸(15-HETE)和11-羟基二十碳四烯酸(11-HETE),所有这些产物的生成均受到1微摩尔消炎痛的抑制。与单独孵育PMN相比,PMN与软骨细胞一起孵育时,从内源性和外源性AA生成的白三烯C4更多,从内源性AA生成的白三烯B4更多,这与软骨细胞中存在白三烯C4合酶和白三烯A4水解酶活性一致。软骨细胞还略微增加了PMN从内源性AA生成的所有5-脂氧合酶(5-LO)衍生产物的水平。
人软骨细胞仅通过环氧化酶途径从AA生成类花生酸。软骨细胞在LT的跨细胞生物合成中发挥协作作用,因为它们具有白三烯A4水解酶和白三烯C4合酶活性,并增加了PMN中5-LO途径的代谢。