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Expression of Mo3e antigen by cultured human umbilical vein endothelial cells (HUVEC) stimulated by phorbol myristate acetate (PMA) and related pharmacological inducers of protein kinase C

机译:培养的人脐静脉内皮细胞(HUVEC)刺激蛋白激酶C刺激的培养人脐静脉内皮细胞(HUVEC)的表达。蛋白激酶C的相关药理学诱导剂

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摘要

Mo3e is a protease-sensitive membrane antigen (p75,50) selectively expressed by human monocytic cells (monocytes and U-937 cells) stimulated in vitro by exposure to a variety of activating factors, including phorbol diester compounds, bacterial lipopolysaccharide (LPS), and muramyl dipeptide (MDP) (R. F. Todd et al., J. Immunol. 135, 3869, 1985). Here we report that primary and multiply-passaged cultures of HUVEC also express the Mo3e determinant after stimulation by phorbol myristate acetate (PMA) and related inducers of protein kinase C. As measured in a radioimmunoassay of anti-Mo3e antibody binding to monolayer cultures of HUVEC, unstimulated cells bore little if any Mo3e. After culture for 4-120 hr in medium containing PMA, 4[beta]-phorbol dibutyrate, 4[beta]-phorbol didecanoate, or mezerein (each at a conentration of 81 nM), or 1-oleoyl-2-acetoyl-sn-3-glycerol (1 mM), HUVEC were found to selectively express the Mo3e determinant. The magnitude of expression was dependent upon the concentration of the stimulus, maximal by 24 hr, and inhibited by cycloheximide. The combination of PMA and the calcium ionophore, ionomycin, had an additive or synergistic effect on HUVEC Mo3e expression. The biologically inactive phorbol compounds 4[beta]-phorbol and 4[alpha]-phorbol didecanoate failed to stimulate Mo3e expression. Also inactive as inducers of HUVEC Mo3e expression were crude lymphokine and monokine supernatants, recombinant human lymphokines (interferon-[gamma] and interleukin-2), recombinant human monokines (interleukin-1 and tumor necrosis factor), bacterial cell wall products including LPS and MDP, pharmacologic agents that increase intracellular cyclic adenosine monophosphate (prostaglandin E2, cholera toxin, theophylline, isoproterenol and isobutylmethylxanthine), lectins (Con A and PHA), and heparin. These results indicate that Mo3e is an inducible plasma membrane antigen of not only mononuclear phagocytes but also cultured HUVEC.
机译:Mo3e是一个蛋白酶敏感的膜抗原(p75,50)由人单核细胞(单核细胞和U-937细胞)中选择性表达在体外刺激通过暴露于多种活化因素,包括佛波醇二酯化合物,细菌脂多糖(LPS),和胞壁酰二肽(MDP)(RF Todd等人,免疫学杂志。135,3869,1985)。这里,我们报告HUVEC的初级和乘法 - 传代培养物中也表达刺激后Mo3e行列式由佛波醇肉豆蔻乙酸酯(PMA)和蛋白质的诱导相关激酶C.如抗Mo3e抗体的放射免疫法测定结合到HUVEC的单层培养物未受刺激的细胞孔几乎没有任何Mo3e。含PMA,4培养4-120小时在介质后的β--phorbol二丁酸酯,4-β-phorbol二癸,或瑞香(每个在81 nM的conentration),或1-油酰-2- acetoyl-SN -3-甘油(1毫米),HUVEC被发现以选择性表达Mo3e决定因素。表达的大小是依赖于刺激的浓度,最大24小时,然后用放线菌酮抑制。 PMA和钙离子载体的结合,离子霉素,对HUVEC Mo3e表达累加或协同效应。无生物活性化合物佛波醇4β] -phorbol和4-α-phorbol二癸未能刺激Mo3e表达。也无活性如HUVEC Mo3e表达的诱导物是粗糙的淋巴因子和单核因子的上清液,重组人淋巴因子(干扰素-γ和白细胞介素-2),重组人单核因子(白介素-1和肿瘤坏死因子),细菌细胞壁产品,包括LPS和MDP,增加细胞内环磷酸腺苷药物制剂(前列腺素E2,霍乱毒素,茶碱,异丙肾上腺素和异丁基),凝集素(Con A的和PHA),和肝素。这些结果表明,Mo3e不仅单核吞噬细胞的可诱导的血浆膜抗原,而且培养HUVEC。

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