Labadia M, Faanes R B, Rothlein R
Department of Immunology, Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, Connecticut 06877.
J Leukoc Biol. 1990 Nov;48(5):420-5. doi: 10.1002/jlb.48.5.420.
Adherence of peritoneal exudate cells (PEC) to plastic has been shown to activate several PEC functions, such as tumor cell lysis and membrane-associated interleukin-1 (mIL-1) expression. Several studies have demonstrated that leukocyte adherence is dependent on divalent cations. In this study, ethylenediaminetetraacetic acid (EDTA), a known chelator of divalent cations, was used to evaluate the role of cell attachment vs. spreading in adherence-induced mIL-1 activity on resident C57BL/6 mouse PEC. Significant inhibition of PEC spreading on plastic and mIL-1 expression was noted when PEC were cultured in the presence of 10 mM EDTA. However, PEC remained adherent in the presence of EDTA and were able to express mIL-1 activity in response to a soluble stimulus lipopolysaccharide (LPS) 1 microgram/ml. These results suggest that the divalent cation-dependent spreading of PEC on plastic initiates or enhances the expression of mIL-1 activity. Additionally, adhesion and LPS stimulate mIL-1 expression by independent mechanisms.
腹膜渗出细胞(PEC)对塑料的黏附已被证明可激活多种PEC功能,如肿瘤细胞裂解和膜相关白细胞介素-1(mIL-1)表达。多项研究表明白细胞黏附依赖于二价阳离子。在本研究中,已知的二价阳离子螯合剂乙二胺四乙酸(EDTA)被用于评估细胞附着与铺展在黏附诱导的mIL-1活性对驻留C57BL/6小鼠PEC中的作用。当PEC在10 mM EDTA存在下培养时,可观察到PEC在塑料上的铺展及mIL-1表达受到显著抑制。然而,PEC在EDTA存在下仍保持黏附,并能够对1微克/毫升的可溶性刺激脂多糖(LPS)作出反应表达mIL-1活性。这些结果表明,PEC在塑料上依赖二价阳离子的铺展启动或增强了mIL-1活性的表达。此外,黏附和LPS通过独立机制刺激mIL-1表达。