首页> 美国卫生研究院文献>International Journal of Biological Sciences >Two Closely Related Human Members of Chitinase-like Family CHI3L1 and CHI3L2 Activate ERK1/2 in 293 and U373 Cells but Have the Different Influence on Cell Proliferation
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Two Closely Related Human Members of Chitinase-like Family CHI3L1 and CHI3L2 Activate ERK1/2 in 293 and U373 Cells but Have the Different Influence on Cell Proliferation

机译:几丁质酶样家族的两个密切相关的人类成员CHI3L1和CHI3L2激活293和U373细胞中的ERK1 / 2但对细胞增殖的影响不同

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摘要

The activation of extracellular signal-regulated kinases (ERK1/2) has been associated with specific outcomes. Sustained activation of ERK1/2 by nerve growth factor (NGF) is associated with translocation of ERKs to the nucleus of PC12 cells and precedes their differentiation into sympathetic-like neurons whereas transient activation by epidermal growth factor (EGF) leads to cell proliferation. It was demonstrated that different growth factors initiating the same cellular signaling pathways may lead to the different cell destiny, either to proliferation or to the inhibition of mitogenesis and apoptosis. Thus, further investigation on kinetic differences in activation of certain signal cascades in different cell types by biologically different agents are necessary for understanding the mechanisms as to how cells make a choice between proliferation and differentiation.It was reported that chitinase 3-like 1 (CHI3L1) protein promotes the growth of human synovial cells as well as skin and fetal lung fibroblasts similarly to insulin-like growth factor 1 (IGF1). Both are involved in mediating the mitogenic response through the signal-regulated kinases ERK1/2. In addition, CHI3L1 which is highly expressed in different tumors including glioblastomas possesses oncogenic properties. As we found earlier, chitinase 3-like 2 (CHI3L2) most closely related to human CHI3L1 also showed increased expression in glial tumors at both the RNA and protein levels and stimulated the activation of the MAPK pathway through phosphorylation of ERK1/2 in 293 and U87 MG cells. The work described here demonstrates the influence of CHI3L2 and CHI3L1 on the duration of MAPK cellular signaling and phosphorylated ERK1/2 translocation to the nucleus. In contrast to the activation of ERK1/2 phosphorylation by CHI3L1 that leads to a proliferative signal (similar to the EGF effect in PC12 cells), activation of ERK1/2 phosphorylation by CHI3L2 (similar to NGF) inhibits cell mitogenesis and proliferation.
机译:细胞外信号调节激酶(ERK1 / 2)的激活与特定的结果有关。神经生长因子(NGF)对ERK1 / 2的持续激活与ERKs向PC12细胞核的移位有关,并先于它们分化为交感神经样细胞,而表皮生长因子(EGF)的瞬时激活导致细胞增殖。已证明启动相同细胞信号传导途径的不同生长因子可能导致不同的细胞命运,从而导致增殖或抑制有丝分裂和凋亡。因此,有必要进一步研究通过生物学不同的试剂激活不同细胞类型的某些信号级联反应的动力学差异,以了解细胞如何在增殖和分化之间做出选择的机制。据报道,几丁质酶3样1(CHI3L1蛋白质类似于胰岛素样生长因子1(IGF1)促进人滑膜细胞以及皮肤和胎儿肺成纤维细胞的生长。两者都参与通过信号调节激酶ERK1 / 2介导有丝分裂反应。另外,在包括胶质母细胞瘤在内的不同肿瘤中高表达的CHI3L1具有致癌特性。正如我们之前所发现的,与人类CHI3L1最密切相关的几丁质酶3样2(CHI3L2)在神经胶质瘤中的RNA和蛋白质水平均表达增加,并通过293和293中ERK1 / 2的磷酸化刺激了MAPK途径的激活。 U87 MG细胞。这里描述的工作证明了CHI3L2和CHI3L1对MAPK细胞信号传导持续时间和磷酸化ERK1 / 2易位至核的影响。与CHI3L1激活ERK1 / 2磷酸化导致增殖信号(类似于PC12细胞中的EGF效应)相反,CHI3L2激活ERK1 / 2磷酸化(类似于NGF)抑制细胞有丝分裂和增殖。

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