Köhler Matthias, Fiebeler Anette, Hartwig Maite, Thiel Sebastian, Prehn Siegfried, Kettritz Ralph, Luft Friedrich C, Hartmann Enno
HELIOS Clinic / Franz Volhard Clinic at the Max Delbrueck Center, Medical Faculty of the Charité, Berlin, Germany.
Cell Physiol Biochem. 2002;12(5-6):335-44. doi: 10.1159/000067903.
We recently cloned six human importin a proteins that transport specific substrates in complex with importin beta into the nucleus. We now compared their absolute expression levels in different human cell lines. We examined their expression regulation during human cell proliferation and differentiation by means of specific antibodies. Proliferation inhibition by starvation of HeLa and HaCaT cells led to a marked decrease in the expression of various nuclear transport factors. In contrast, re-addition of serum increased alpha-importin expression. We analyzed two models for cell differentiation and found differential importin regulation. Stimulation of rat pancreatic AR42J cell differentiation towards a neuroendocrine phenotype with activin A or towards an acinar phenotype with dexamethasone, caused strong upregulation of importin alpha3 and alpha4 expression. Phorbol ester-induced differentiation of human leukemia (HL60) cells towards a macrophage phenotype led to downregulation of importin alpha1 and alpha4 expression after 72 hours. Similarly, importins alpha1 and alpha4 displayed a strong downregulation when HL60 cells were directed towards a neutrophil phenotype by DMSO treatment. This study is the first to assess all the human importin alpha isoforms in documenting differential nuclear transport factor regulation during cell proliferation and differentiation.
我们最近克隆了六种人类输入蛋白α,它们与输入蛋白β形成复合物,将特定底物转运到细胞核中。我们现在比较了它们在不同人类细胞系中的绝对表达水平。我们通过特异性抗体研究了它们在人类细胞增殖和分化过程中的表达调控。饥饿抑制HeLa和HaCaT细胞增殖导致多种核转运因子的表达显著降低。相反,重新添加血清会增加α-输入蛋白的表达。我们分析了两种细胞分化模型,发现输入蛋白的调控存在差异。用激活素A刺激大鼠胰腺AR42J细胞向神经内分泌表型分化,或用地塞米松刺激其向腺泡表型分化,都会导致输入蛋白α3和α4表达的强烈上调。佛波酯诱导人白血病(HL60)细胞向巨噬细胞表型分化,72小时后导致输入蛋白α1和α4表达下调。同样,当HL60细胞通过二甲基亚砜处理定向分化为中性粒细胞表型时,输入蛋白α1和α4也表现出强烈下调。本研究首次评估了所有人类输入蛋白α异构体,以记录细胞增殖和分化过程中核转运因子的差异调控。