兔炎症部位白细胞介素- 1 β的生物合成:动力学和生成细胞。

F Goto, K Goto, S Mori, S Ohkawara, M Yoshinaga
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引用次数: 0

摘要

研究炎症性腹膜渗出细胞(PEC)合成白细胞介素- 1 β (il - 1 β)的生物活性(胸腺细胞共丝分裂测定)、il - 1 β mRNA表达(细胞质槽点印迹分析)和免疫反应性il - 1 β分子检测(免疫细胞化学)。我们的研究结果表明,仅在早期炎症部位的PEC中观察到il - 1 β的表达,并且炎症过程中il - 1 β活性的动力学特征可以通过il - 1 β mRNA的表达来解释,即炎症渗出细胞的重新合成。在单细胞水平上,我们明确地证明了在酪蛋白诱导的兔急性炎症过程中,多形核白细胞是il - 1 β的主要产生者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biosynthesis of interleukin-I beta at inflammatory site in rabbits: kinetics and producing cells.

Biosynthesis of interleukin-I beta (IL-I beta) by inflammatory peritoneal exudate cells (PEC) was studied in terms of biological activity (thymocyte co-mitogenic assay), IL-I beta mRNA expression (cytoplasmic slot blot analysis) and detection of immunoreactive IL-I beta molecule (immunocytochemistry). Our findings were taken to conclude that IL-I beta expression was observed only in PEC harvested from early inflammatory site and the kinetic profile of the IL-I activity during the course of the inflammation was explained by IL-I beta mRNA expression, namely de-novo synthesis by inflammatory exudate cells. With respect to a single cell level, it was definitely proved that polymorphonuclear leucocytes were the major producer of IL-I beta during the casein-induced acute inflammation in rabbits.

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