Todd R F, Bury M J, Alvarez P A, Brott D A, Liu D Y
Blood. 1986 Nov;68(5):1154-61.
Mo3e is a protein (p 50,80) that is expressed on the surface of human monocytic cells after exposure in vitro to soluble activating factors that include bacterial lipopolysaccharide, muramyl dipeptide, and phorbol myristate acetate (PMA). The surface expression of Mo3e may represent a cellular event that occurs in response to the formation of "secondary messengers" that include diacylglycerol, inositol trisphosphate, and calcium ions. This postulate is based on the stimulatory effect of agents that can mimic the activity of endogenous diacylglycerol (PMA and other biologically active phorbol compounds, mezerein, and L-alpha-1,2 dioctanoylglycerol) and inositol trisphosphate (ionomycin) on Mo3e expression by U-937 and HL-60 cells. The inhibitory effect of phospholipid-active calmodulin inhibitors (trifluoperazine, chlorpromazine, and dibucaine), calcium antagonists (nicardipine and TMB-8), and EGTA further support the involvement of phospholipid- and calcium-dependent protein kinase (protein kinase C) and calcium ions in the up-modulation of Mo3e surface expression.
Mo3e是一种蛋白质(分子量50,80),在体外暴露于包括细菌脂多糖、胞壁酰二肽和佛波醇肉豆蔻酸酯乙酸酯(PMA)在内的可溶性激活因子后,会在人单核细胞表面表达。Mo3e的表面表达可能代表一种细胞事件,它是对包括二酰基甘油、肌醇三磷酸和钙离子在内的“第二信使”形成的反应。这一假设基于能够模拟内源性二酰基甘油(PMA和其他生物活性佛波醇化合物、大戟二萜醇、L-α-1,2-二辛酰甘油)和肌醇三磷酸(离子霉素)活性的试剂对U-937和HL-60细胞中Mo3e表达的刺激作用。磷脂活性钙调蛋白抑制剂(三氟拉嗪、氯丙嗪和丁卡因)、钙拮抗剂(尼卡地平和平喘新)以及乙二醇双(2-氨基乙基醚)四乙酸(EGTA)的抑制作用进一步支持了磷脂依赖性和钙依赖性蛋白激酶(蛋白激酶C)以及钙离子参与Mo3e表面表达上调的过程。