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人近端肾小管上皮细胞体外白细胞介素6的产生:白细胞介素-1α(IL-1α)及其他细胞因子的作用分析

Interleukin 6 production by human proximal tubular epithelial cells in vitro: analysis of the effects of interleukin-1 alpha (IL-1 alpha) and other cytokines.

作者信息

Boswell R N, Yard B A, Schrama E, van Es L A, Daha M R, van der Woude F J

机构信息

Department of Nephrology, University Hospital, Leiden, The Netherlands.

出版信息

Nephrol Dial Transplant. 1994;9(6):599-606. doi: 10.1093/ndt/9.6.599.

Abstract

Proximal tubular epithelial cells (PTEC) from human renal tissue obtained from biopsy or nephrectomy were grown in monoculture and evaluated in vitro at passage 2-4 for interleukin 6 (IL-6) production in response to medium alone or to interleukin 1 alpha (IL-1 alpha), tumour necrosis factor alpha (TNF alpha), interleukin 2 (IL-2), interferon gamma (INF gamma) or lipopolysaccharide (LPS). IL-6 bioactivity was quantitated using the IL-6-dependent murine hybridoma cell line (B9) and expressed as IL-6 units/ml/10(5) PTEC. PTEC cell lines exposed to medium alone produced intermediate amounts of IL-6 with substantial variability between cell lines. Introduction of IL-1 alpha resulted in a dose- and time-dependent increase in IL-6 production by PTEC that was maximal at 1 ng/ml IL-1 alpha at 24 h. All PTEC cell lines showed an increased IL-6 production on exposure to IL-1 alpha varying from 1.3- to 24-fold increase over baseline production. This response was completely blocked by anti-rIL-1 alpha. No significant IL-6 production by PTEC could be induced by TNF alpha, IL-2, IFN gamma, or LPS over a broad dosage range. Cycloheximide inhibited IL-6 production without irreversible cell toxicity, indicating de-novo synthesis. IL-6 produced by PTEC had a molecular weight of 26-29 kDa as demonstrated by Western blot analysis. Using PCR analysis we could demonstrate upregulation by IL-1 alpha of IL-6 mRNA in a dose-response fashion, indicating that IL-1 alpha regulates IL-6 production at a pretranslational value of protein synthesis.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

从活检或肾切除获得的人肾组织中的近端肾小管上皮细胞(PTEC)进行单培养,并在传代2 - 4时进行体外评估,以检测其对单独培养基或白细胞介素1α(IL - 1α)、肿瘤坏死因子α(TNFα)、白细胞介素2(IL - 2)、干扰素γ(INFγ)或脂多糖(LPS)的白细胞介素6(IL - 6)产生情况。使用依赖IL - 6的小鼠杂交瘤细胞系(B9)对IL - 6生物活性进行定量,并表示为IL - 6单位/毫升/10⁵ PTEC。单独暴露于培养基的PTEC细胞系产生中等量的IL - 6,细胞系之间存在很大差异。引入IL - 1α导致PTEC产生IL - 6呈剂量和时间依赖性增加,在24小时时1 ng/ml IL - 1α时达到最大值。所有PTEC细胞系在暴露于IL - 1α时IL - 6产生增加,比基线产生增加1.3至24倍。该反应被抗rIL - 1α完全阻断。在广泛的剂量范围内,TNFα、IL - 2、IFNγ或LPS不能诱导PTEC产生显著的IL - 6。放线菌酮抑制IL - 6产生且无不可逆细胞毒性,表明是从头合成。蛋白质印迹分析表明,PTEC产生的IL - 6分子量为26 - 29 kDa。使用PCR分析,我们可以证明IL - 1α以剂量反应方式上调IL - 6 mRNA,表明IL - 1α在蛋白质合成的翻译前水平调节IL - 6的产生。(摘要截断于250字)

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