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人腹膜间皮细胞合成白细胞介素-6:由白细胞介素-1β和肿瘤坏死因子α诱导产生。

Human peritoneal mesothelial cells synthesize interleukin-6: induction by IL-1 beta and TNF alpha.

作者信息

Topley N, Jörres A, Luttmann W, Petersen M M, Lang M J, Thierauch K H, Müller C, Coles G A, Davies M, Williams J D

机构信息

Institute of Nephrology, University of Wales College of Medicine, Cardiff Royal Infirmary, Wales, United Kingdom.

出版信息

Kidney Int. 1993 Jan;43(1):226-33. doi: 10.1038/ki.1993.36.

Abstract

Recent studies have demonstrated increased levels of IL-6 in the peritoneal cavity during CAPD peritonitis. The current investigation was initiated (i) to examine the human peritoneal mesothelial cell (HPMC) as a possible source of this secreted IL-6 and (ii) to characterize the released product and examine its regulation by other cytokines. Unstimulated HPMC under growth arrested conditions released IL-6 in a time dependent manner. After 24-hour HPMC IL-6 release (mean +/- SEM, N = 13) (expressed as pg/micrograms cell protein) was 1.67 +/- 0.33. Stimulation of HPMC with IL-1 beta or TNF alpha resulted in a time (increasing up to 48 hr) and dose dependent IL-6 generation. After 24 hours the levels induced by IL-1 beta and TNF alpha (both at 1000 pg/ml) were (mean +/- SEM, N = 13) 19.08 +/- 2.98 and 6.62 +/- 1.72, respectively. Stimulation with combinations of IL-1 beta and TNF alpha resulted in additive increases in IL-6 release. This release could be inhibited by co-incubation with anti-IL-1 beta and/or anti-TNF alpha antibodies. The level of released HPMC IL-6 measured by immunometric assay (ELISA) correlated directly with that detected in the 7TD1 IL-6 bioassay (r = 0.63; P < 0.001). Western blot analysis of concentrated HPMC supernatants using specific anti-IL-6 antibody demonstrated immunoreactive bands at 23 and 28 Kd following IL-1 beta or TNF alpha treatment.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

最近的研究表明,持续性非卧床腹膜透析(CAPD)腹膜炎期间腹腔内白细胞介素-6(IL-6)水平升高。本研究旨在:(i)检测人腹膜间皮细胞(HPMC)是否可能是这种分泌型IL-6的来源;(ii)鉴定释放产物并检测其他细胞因子对其的调节作用。生长停滞条件下未受刺激的HPMC以时间依赖性方式释放IL-6。24小时后HPMC释放的IL-6(平均值±标准误,N = 13)(以pg/μg细胞蛋白表示)为1.67±0.33。用IL-1β或肿瘤坏死因子-α(TNF-α)刺激HPMC导致IL-6生成呈时间(至48小时增加)和剂量依赖性。24小时后,IL-1β和TNF-α(均为1000 pg/ml)诱导的水平(平均值±标准误,N = 13)分别为19.08±2.98和6.62±1.72。用IL-1β和TNF-α联合刺激导致IL-6释放呈累加性增加。这种释放可通过与抗IL-1β和/或抗TNF-α抗体共同孵育来抑制。通过免疫测定法(ELISA)测定的HPMC释放的IL-6水平与在7TD1 IL-6生物测定中检测到的水平直接相关(r = 0.63;P < 0.001)。使用特异性抗IL-6抗体对浓缩的HPMC上清液进行蛋白质印迹分析显示,IL-1β或TNF-α处理后在23和28 Kd处出现免疫反应条带。(摘要截短于250字)

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