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星形胶质细胞释放的一种产物对培养的脑内皮细胞中γ-谷氨酰转肽酶的诱导作用。

Induction of gamma-glutamyl transpeptidase in cultured cerebral endothelial cells by a product released by astrocytes.

作者信息

Maxwell K, Berliner J A, Cancilla P A

出版信息

Brain Res. 1987 May 5;410(2):309-14. doi: 10.1016/0006-8993(87)90329-5.

Abstract

gamma-Glutamyl transpeptidase (gamma GTP) is an enzyme found in cerebral capillary endothelial cells, the presumed site of the blood-brain barrier, but not in endothelial cells lining blood vessels in other parts of the body. Using a line of mouse cerebral microvessel endothelial cells (ME-ly cells) and a sensitive colorimetric assay to measure gamma GTP levels we demonstrated that primary cultures of mouse astrocytes and a line of rat C6 glioma cells released a soluble product(s) that induced the production of gamma GTP in cultured endothelial cells by 34% and 39%, respectively, over control levels. Cerebrovascular smooth muscle cells had no significant effect on gamma GTP levels in ME-ly cells, and the astrocyte product(s) had no effect on rabbit aortic endothelial cells. The induction of gamma GTP levels in ME-ly cells was apparent after one day of exposure to the astrocyte product(s) and increased in magnitude with increasing time of exposure of the ME-ly cells to the product(s). Removal of the product(s) from the ME-ly cells resulted in a return to control levels of gamma GTP in the ME-ly cells within 2 days. The presence of a protein synthesis inhibitor during incubation with the product(s) blocked the induction of gamma GTP in ME-ly cells, and treatment of the product(s) with 200 U/ml TPCK-trypsin destroyed its inductive properties.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

γ-谷氨酰转肽酶(γ-GTP)是一种存在于脑毛细血管内皮细胞中的酶,脑毛细血管内皮细胞被认为是血脑屏障的所在部位,但在身体其他部位的血管内皮细胞中不存在。我们使用小鼠脑微血管内皮细胞系(ME-ly细胞)和一种灵敏的比色测定法来测量γ-GTP水平,结果表明,原代培养的小鼠星形胶质细胞系和大鼠C6胶质瘤细胞释放出一种可溶性产物,该产物可使培养的内皮细胞中γ-GTP的产生量分别比对照水平提高34%和39%。脑血管平滑肌细胞对ME-ly细胞中γ-GTP水平无显著影响,星形胶质细胞产物对兔主动脉内皮细胞也无影响。ME-ly细胞在接触星形胶质细胞产物一天后,γ-GTP水平的诱导作用就很明显,并且随着ME-ly细胞接触该产物时间的增加,诱导作用的幅度也增大。从ME-ly细胞中去除该产物后,ME-ly细胞中的γ-GTP水平在2天内恢复到对照水平。在与该产物孵育期间加入蛋白质合成抑制剂可阻断ME-ly细胞中γ-GTP的诱导作用,用200 U/ml的TPCK-胰蛋白酶处理该产物会破坏其诱导特性。(摘要截短于250字)

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