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Dictyostelium stress-activated protein kinase alpha, a novel stress-activated mitogen-activated protein kinase kinase kinase-like kinase, is important for the proper regulation of the cytoskeleton

机译:Dictyostelium应激激活的蛋白激酶α,一种新型的应激激活的促分裂原激活的蛋白激酶激酶样激酶,对细胞骨架的适当调节很重要

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Mitogen-activated protein kinase cascades regulate various cellular functions, including growth, cell differentiation, development, and stress responses. We have identified a new Dictyostelium kinase (stress-activated protein kinase [SAPK]a), which is related to members of the mixed lineage kinase class of mitogen-activated protein kinase kinases. SAPKalpha is activated by osmotic stress, heat shock, and detachment from the substratum and by a membrane-permeable cGMP analog, a known regulator of stress responses in Dictyostelium. SAPKalpha is important for cellular resistance to stresses, because SAPKalpha null cells exhibit reduced viability in response to osmotic stress. We found that SAPKalpha mutants affect cellular processes requiring proper regulation of the actin cytoskeleton, including cell motility, morphogenesis, cytokinesis, and cell adhesion. Overexpression of SAPKalpha results in highly elevated basal and chemoattractant-stimulated F-actin levels and strong aggregation and developmental defects, including a failure to polarize and chemotax, and abnormal morphogenesis. These phenotypes require a kinase-active SAPKalpha. SAPKalpha null cells exhibit reduced chemoattractant-stimulated F-actin levels, cytokinesis, developmental and adhesion defects, and a motility defect that is less severe than that exhibited by SAPKalpha-overexpressing cells. SAPK colocalizes with F-actin in F-actin-enriched structures, including membrane ruffles and pseudopodia during chemotaxis. Although SAPKa is required for these F-actin-mediated processes, it is not detectably activated in response to chemoattractant stimulation. [References: 77]
机译:丝裂原活化的蛋白激酶级联反应调节各种细胞功能,包括生长,细胞分化,发育和应激反应。我们已经确定了一种新的Dictyostelium激酶(应激激活的蛋白激酶[SAPK] a),它与有丝分裂原激活的蛋白激酶激酶的混合谱系激酶成员有关。 SAPKalpha被渗透压,热休克和与基底的分离以及膜通透性cGMP类似物(已知的Dictyostelium应激反应调节剂)激活。 SAPKalpha对于细胞对压力的抵抗力很重要,因为SAPKalpha空细胞在对渗透压力的反应中表现出降低的生存能力。我们发现,SAPKalpha突变体影响需要适当调节肌动蛋白细胞骨架的细胞过程,包括细胞运动,形态发生,胞质分裂和细胞粘附。 SAPKalpha的过表达导致高度增加的基础和趋化因子刺激的F-肌动蛋白水平,以及强的聚集和发育缺陷,包括极化和化学趋化失败以及异常的形态发生。这些表型需要激酶活性的SAPKalpha。 SAPKalpha空细胞表现出降低的趋化因子刺激的F-肌动蛋白水平,胞质分裂,发育和粘附缺陷,以及运动性缺陷,其严重程度低于SAPKalpha过表达细胞。在趋化过程中,SAPK在富含F-肌动蛋白的结构(包括膜褶和伪足)中与F-肌动蛋白共定位。尽管SAPKa是这些F-肌动蛋白介导的过程所必需的,但它不能响应化学引诱剂刺激而被可检测地激活。 [参考:77]

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