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Roles of PLC-β2 and -β3 and PI3Kγ in Chemoattractant-Mediated Signal Transduction

机译:PLC-β2和-β3和PI3Kγ在趋化因子介导的信号转导中的作用

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摘要

The roles of phosphoinositide 3-kinase (PI3K) and phospholipase C (PLC) in chemoattractant-elicited responses were studied in mice lacking these key enzymes. PI3Kγ was required for chemoattractant-induced production of phos-phatidylinositol 3,4,5-trisphosphate [PtdIns (3,4,5)P_3] and has an important role in chemoattractant-induced superoxide production and chemotaxis in mouse neutrophils and in production of T cell-independent antigen-specific antibodies composed of the immunoglobulin λ light chain (TI-Igλ_L). The study of the mice lacking PLC-β2 and -β3 revealed that the PLC pathways have an important role in chemoattractant-mediated production of superoxide and regulation of protein kinases, but not chemotaxis. The PLC pathways also appear to inhibit the chemotactic activity induced by certain chemoattractants and to suppress TI-Igλ_L production.
机译:在缺乏这些关键酶的小鼠中研究了磷酸肌醇3-激酶(PI3K)和磷脂酶C(PLC)在趋化因子引起的反应中的作用。 PI3Kγ是化学引诱剂诱导的磷脂酰肌醇3,4,5-三磷酸[PtdIns(3,4,5)P_3]所必需的,并且在化学诱导剂诱导的小鼠中性粒细胞的超氧化物的产生和趋化性以及在小鼠中性粒细胞的产生中具有重要作用。 T细胞非依赖性抗原特异性抗体,由免疫球蛋白λ轻链(TI-Igλ_L)组成。对缺乏PLC-β2和-β3的小鼠的研究表明,PLC途径在趋化因子介导的超氧化物的产生和蛋白激酶的调控中具有重要作用,但对趋化性没有影响。 PLC途径似乎也抑制某些趋化因子诱导的趋化活性并抑制TI-Igλ_L的产生。

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