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脂多糖诱导早孕滋养层细胞系中细胞因子的表达及翻译后表达

Induction and posttranslational expression of cytokines in a first-trimester trophoblast cell line by lipopolysaccharide.

作者信息

Svinarich D M, Bitonti O M, Romero R, Gonik B

机构信息

Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI 48201, USA.

出版信息

Am J Obstet Gynecol. 1996 Oct;175(4 Pt 1):970-3. doi: 10.1016/s0002-9378(96)80034-2.

Abstract

OBJECTIVES

The response to infection by human first-trimester trophoblasts is a poorly understood event. This study was undertaken to determine whether first-trimester trophoblasts are capable of responding to an infection stimulus and mediating an immune response.

STUDY DESIGN

HTR-8/SVneo cells were exposed to lipopolysaccharide (1 microgram/ml) or media alone for either 0, 2, 4, 6, 8, or 24 hours. Northern analysis was conducted by use of a panel of antisense cytokine probes. Enzyme-linked immunosorbent assays specific for either interleukin-1 alpha, interleukin-6, interleukin-8, or transforming growth factor-beta 1 were conducted on corresponding cell culture supernatants, and the kinetics of expression were determined.

RESULTS

Interleukin-1 alpha, interleukin-6, interleukin-8, and transforming growth factor-beta 1 transcription occurred maximally between 2 and 8 hours of culture in media containing lipopolysaccharide, with a subsequent diminution of response. Enzyme-linked immunosorbent assay analysis corroborated lipopolysaccharide induction seen at the level of transcription, with significant posttranslational expression of these cytokines being detected between 2 and 24 hours in culture (p < 0.01).

CONCLUSIONS

Expression of the proinflammatory cytokines interleukin-1 alpha, interleukin-6, interleukin-8 and transforming growth factor-beta 1 strongly support the contention that human first-trimester trophoblasts are capable of responding to an infection stimulus and eliciting an immune response through cytokine-based immune signaling.

摘要

目的

人类孕早期滋养层细胞对感染的反应是一个尚未被充分了解的过程。本研究旨在确定孕早期滋养层细胞是否能够对感染刺激做出反应并介导免疫反应。

研究设计

将HTR-8/SVneo细胞暴露于脂多糖(1微克/毫升)或单独的培养基中0、2、4、6、8或24小时。使用一组反义细胞因子探针进行Northern分析。对相应的细胞培养上清液进行针对白细胞介素-1α、白细胞介素-6、白细胞介素-8或转化生长因子-β1的酶联免疫吸附测定,并确定表达动力学。

结果

在含有脂多糖的培养基中培养2至8小时期间,白细胞介素-1α、白细胞介素-6、白细胞介素-8和转化生长因子-β1的转录达到最大值,随后反应减弱。酶联免疫吸附测定分析证实了在转录水平上观察到的脂多糖诱导,在培养2至24小时之间检测到这些细胞因子的显著翻译后表达(p < 0.01)。

结论

促炎细胞因子白细胞介素-1α、白细胞介素-6、白细胞介素-8和转化生长因子-β1的表达有力地支持了以下观点,即人类孕早期滋养层细胞能够对感染刺激做出反应,并通过基于细胞因子的免疫信号传导引发免疫反应。

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