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植物血凝素和白细胞介素-1转导信号之间的相互关系。

Interrelationship between signals transduced by phytohemagglutinin and interleukin 1.

作者信息

Mills G B, Hill M, McGill M, May C, Stanley J, Stewart D J, Mellors A, Gelfand E W

机构信息

Oncology Research, Toronto General Hospital, Ontario, Canada.

出版信息

J Cell Physiol. 1990 Mar;142(3):539-51. doi: 10.1002/jcp.1041420313.

Abstract

In the murine cell line LBRM-331A5, phytohemagglutinin (PHA) induces secretion of the T cell growth factor interleukin 2 (IL2). IL1 augments PHA-induced IL2 production. In this cell line, PHA stimulates a number of biochemical changes including phospholipid hydrolysis, increases in cytosolic free calcium [( Ca2+]i), membrane hyperpolarization, cytosolic alkalinization, and tyrosine phosphorylation of specific substrates. Using LBRM cells, we have studied the interrelationship between these events and the secretion of IL2. Increases in [Ca2+]i triggered by PHA or following addition of ionomycin result in membrane hyperpolarization but are not required for PHA-induced cytosolic alkalinization or tyrosine phosphorylation. Addition of IL1 to PHA-stimulated cells did not affect any of the biochemical parameters, although it significantly augmented PHA-induced IL2 secretion. Increasing [Ca2+]i with ionomycin did not trigger IL2 secretion, increases in cytosolic pH, or tyrosine phosphorylation in the presence or absence of IL1. Preventing increases in cytosolic pH did not alter PHA-induced changes in [Ca2+]i or membrane potential. These data are compatible with PHA including activation of phospholipase C and production of inositol phosphates resulting in both release of Ca2+ from internal stores and transmembrane uptake of Ca2+ as well as activation of protein kinase C. However, unlike other growth factor or mitogen-stimulated systems, the changes stimulated by PHA and IL1 in LBRM cells including IL2 secretion are not regulated by a pertussis toxin-sensitive G protein.

摘要

在鼠细胞系LBRM - 331A5中,植物血凝素(PHA)可诱导T细胞生长因子白细胞介素2(IL2)的分泌。IL1可增强PHA诱导的IL2产生。在该细胞系中,PHA可刺激一些生化变化,包括磷脂水解、胞质游离钙([Ca2+]i)增加、膜超极化、胞质碱化以及特定底物的酪氨酸磷酸化。利用LBRM细胞,我们研究了这些事件与IL2分泌之间的相互关系。PHA引发的或添加离子霉素后[Ca2+]i的增加会导致膜超极化,但PHA诱导的胞质碱化或酪氨酸磷酸化并不需要[Ca2+]i的增加。向PHA刺激的细胞中添加IL1并不影响任何生化参数,尽管它显著增强了PHA诱导的IL2分泌。在有或没有IL1存在的情况下,用离子霉素增加[Ca2+]i均不会引发IL2分泌、胞质pH升高或酪氨酸磷酸化。阻止胞质pH升高并不会改变PHA诱导的[Ca2+]i或膜电位变化。这些数据与PHA包括激活磷脂酶C和产生肌醇磷酸,从而导致Ca2+从内部储存库释放以及Ca2+跨膜摄取以及蛋白激酶C的激活是一致的。然而,与其他生长因子或有丝分裂原刺激的系统不同,PHA和IL1在LBRM细胞中刺激的变化,包括IL2分泌,不受百日咳毒素敏感G蛋白的调节。

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