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新型粒细胞钙(++)/钙调蛋白依赖性激酶CKLiK的鉴定与特性分析

Identification and characterization of CKLiK, a novel granulocyte Ca(++)/calmodulin-dependent kinase.

作者信息

Verploegen S, Lammers J W, Koenderman L, Coffer P J

机构信息

Department of Pulmonary Diseases, University Medical Centre Utrecht, 3584 CX Utrecht, The Netherlands.

出版信息

Blood. 2000 Nov 1;96(9):3215-23.

Abstract

Human granulocytes are characterized by a variety of specific effector functions involved in host defense. Several widely expressed protein kinases have been implicated in the regulation of these effector functions. A polymerase chain reaction-based strategy was used to identify novel granulocyte-specific kinases. A novel protein kinase complementary DNA with an open reading frame of 357 amino acids was identified with homology to calcium-calmodulin-dependent kinase I (CaMKI). This has been termed CaMKI-like kinase (CKLiK). Analysis of CKLiK messenger RNA (mRNA) expression in hematopoietic cells demonstrated an almost exclusive expression in human polymorphonuclear leukocytes (PMN). Up-regulation of CKLiK mRNA occurs during neutrophilic differentiation of CD34(+) stem cells. CKLiK kinase activity was dependent on Ca(++) and calmodulin as analyzed by in vitro phosphorylation of cyclic adenosine monophosphate responsive element modulator (CREM). Furthermore, CKLiK- transfected cells treated with ionomycin demonstrated an induction of CRE- binding protein (CREB) transcriptional activity compared to control cells. Additionally, CaMK-kinasealpha enhanced CKLiK activity. In vivo activation of CKLiK was shown by addition of interleukin (IL)-8 to a myeloid cell line stably expressing CKLiK. Furthermore inducible activation of CKLiK was sufficient to induce extracellular signal-related kinase (ERK) mitogen-activated protein (MAP) kinase activity. These data identify a novel Ca(++)/calmodulin-dependent PMN- specific kinase that may play a role in Ca(++)-mediated regulation of human granulocyte functions.

摘要

人类粒细胞具有多种参与宿主防御的特定效应功能。几种广泛表达的蛋白激酶与这些效应功能的调节有关。采用基于聚合酶链反应的策略来鉴定新型粒细胞特异性激酶。鉴定出一种新型蛋白激酶互补DNA,其开放阅读框为357个氨基酸,与钙调蛋白依赖性激酶I(CaMKI)具有同源性。这被称为CaMKI样激酶(CKLiK)。对造血细胞中CKLiK信使核糖核酸(mRNA)表达的分析表明,其几乎只在人类多形核白细胞(PMN)中表达。在CD34(+)干细胞的嗜中性分化过程中,CKLiK mRNA上调。通过环磷酸腺苷反应元件调节剂(CREM)的体外磷酸化分析,CKLiK激酶活性依赖于Ca(++)和钙调蛋白。此外,与对照细胞相比,用离子霉素处理的CKLiK转染细胞显示出CRE结合蛋白(CREB)转录活性的诱导。另外,CaMK激酶α增强了CKLiK活性。向稳定表达CKLiK的髓系细胞系中添加白细胞介素(IL)-8可显示CKLiK在体内的激活。此外,CKLiK的诱导激活足以诱导细胞外信号相关激酶(ERK)丝裂原活化蛋白(MAP)激酶活性。这些数据鉴定出一种新型的Ca(++)/钙调蛋白依赖性PMN特异性激酶,其可能在Ca(++)介导的人类粒细胞功能调节中发挥作用。

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