IL-1、ICAM-1、LFA-3和氢化可的松对人胎儿胸腺上皮细胞分泌细胞因子的调节存在差异。

Thymus Pub Date : 1996-01-01
S Shu, P Naylor, J L Touraine, J W Hadden
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引用次数: 0

摘要

在无血清条件下培养人胎儿胸腺上皮细胞(TEC)。采用ELISA法检测TEC中14c标记肽的分泌情况以及IL-3、IL-6、IL-7、IL-8、GM-CSF、LIF、纤维连接蛋白和胸腺素α 1的分泌情况。这些TEC未检测到IL-3和IL-7。缺乏IL-7和胸腺素α 1和表面分子TE-4的存在将这些细胞描述为包膜下/髓质TEC。TEC组构性分泌IL-6、IL-8、纤维连接蛋白和胸腺素α 1,但不分泌LIF的GM-CSF。刺激物包括重组IL-1和表面粘附分子ICAM-1和af -3的单克隆抗体。此外,氢化可的松(2.7 x 10(-7) M)用于解剖分泌模式。重组IL-1、抗ICAM-1和抗LFA-3单独和共同诱导14c标记肽和IL-6和IL-8的分泌适度但显著增加,而HC不抑制这些分泌。重组IL-1而非抗ICAM-1和抗LFA-3诱导GM-CSF和LIF。HC抑制IL-1诱导的GM-CSF和LIF的分泌。没有一种兴奋剂增加纤维连接蛋白或胸腺素α 1的组成分泌,HC抑制胸腺素α 1的分泌。TEC分泌细胞因子,而不是胸腺素α 1和纤维连接蛋白,似乎以比迄今为止认识到的更复杂的方式调节。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
IL-1, ICAM-1, LFA-3, and hydrocortisone differentially regulate cytokine secretion by human fetal thymic epithelial cells.

Human fetal thymic epithelial cells (TEC) were cultured under serum-free conditions. The TEC were analyzed for the secretion of 14C-labelled peptides and of IL-3, IL-6 IL-7, IL-8, GM-CSF, LIF, fibronectin and thymosin alpha 1 by ELISA tests. IL-3 and IL-7 were not detected from these TEC. Lack of IL-7 and presence of thymosin alpha 1 and of the surface molecule TE-4 depicts these cells as subcapsular/medullary TEC. TEC secreted constitutively IL-6, IL-8, fibronectin and thymosin alpha 1 but not GM-CSF of LIF. Stimulants included recombinant IL-1 and monoclonal antibodies to the surface adhesion molecules ICAM-1 and LAF-3. In addition, hydrocortisone (2.7 x 10(-7) M) was used to dissect secretion patterns. Recombinant IL-1, anti ICAM-1, and anti LFA-3 alone and collectively induced modest but significant increases in the secretions of 14C-labelled peptides and of IL-6 and IL-8 which were not inhibited by HC. Recombinant IL-1 but not anti ICAM-1 and anti LFA-3 induced GM-CSF and LIF. HC inhibited the secretion of GM-CSF and LIF induced by IL-1. None of the stimulants augmented the constitutive secretion of fibronectin or thymosin alpha 1 and HC inhibited thymosin alpha 1 secretion. TEC secretion of cytokines but not thymosin alpha 1 and fibronectin appear to be regulated in a more complex manner than heretofore recognized.

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