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Pigment epithelium-derived factor plays an inhibitory role in proliferation and migration of HaCaT cells

机译:色素上皮衍生因子在HaCaT细胞增殖和迁移中起抑制作用

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The normal vasculature is maintained by a balance between angiogenic factors and anti-angiogenic factors. Recent studies have shown that pigment epithelium-derived factor (PEDF) can induce differentiation and inhibit angiogenesis of tumors. This study was designed to investigate the expression of PEDF and its roles in proliferation, adhesion and migration of HaCaT cells, a human keratinocyte cell line. Our results have shown that PEDF is expressed in HaCaT cells at both mRNA and protein levels determined by RT-PCR and Western blot, separately. PEDF signal mainly localizes in the cytoplasm of HaCaT cell, as determined by immunofluorescence. Furthermore, expression of PEDF is decreased by 50 ng/ml of VEGF165. Proliferation and migration of HaCaT cells are decreased by PEDF, while adhesion of HaCaT cells is upregulated approximately by 29%. PEDF also induce the S phase accumulation of HaCaT cells. In addition, phosphorylation of ERK1/2, not JNK and p38, is decreased by PEDF. These results indicate that PEDF may play an inhibitory role on growth and migration of HaCaT cells through dephosphorylation of ERK1/2.
机译:通过血管生成因子和抗血管生成因子之间的平衡来维持正常的脉管系统。最近的研究表明,色素上皮衍生因子(PEDF)可以诱导分化并抑制肿瘤的血管生成。这项研究旨在调查PEDF的表达及其在人角质形成细胞系HaCaT细胞增殖,粘附和迁移中的作用。我们的结果表明,PEDF在HaCaT细胞中分别通过RT-PCR和Western blot测定在mRNA和蛋白水平上表达。通过免疫荧光测定,PEDF信号主要位于HaCaT细胞的细胞质中。此外,PEDF的表达降低了50 ng / ml的VEGF 165 。 PEDF减少了HaCaT细胞的增殖和迁移,而HaCaT细胞的粘附性则上调了约29%。 PEDF还诱导HaCaT细胞的S期积累。此外,PEDF可以减少ERK1 / 2而不是JNK和p38的磷酸化。这些结果表明,PEDF可能通过ERK1 / 2的去磷酸化对HaCaT细胞的生长和迁移起抑制作用。

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