南方医科大学学报 ›› 2015, Vol. 35 ›› Issue (09): 1245-.

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核因子I-C 降低皮肤成纤维细胞对TGF-β的敏感性

张亮平,王洋,雷睿,沈辉,沈毅忱,吴智南,徐靖宏   

  • 出版日期:2015-09-20 发布日期:2015-09-20

Nuclear factor I-C inhibits platelet-derived growth factor-induced enhancement of
dermal fibroblast sensitivity to TGF-β

  • Online:2015-09-20 Published:2015-09-20

摘要: 目的探讨核因子I-C(NFI-C)对血小板源性生长因子(PDGF)促进皮肤成纤维细胞表达TGF-β受体Ⅱ(TβRⅡ)作用的影
响。方法含有NFI-C序列的慢病毒转染人皮肤成纤维细胞(HFF-1);根据细胞生长活性及转染效率筛选最佳转染复数(MOI);
PDGF-BB刺激体外培养的HFF-1细胞、转染NFI-C的HFF-1细胞以及转染阴性病毒的HFF-1细胞,并设立转染NFI-C但不用
PDGF处理的细胞;以不做任何处理的HFF-1 细胞作为空白对照组;采用western blot、RT-qPCR测定各组细胞TβRⅡ的表达。
数据采用单因素方差分析、LSD-t及SNK-q检验对各组数据进行分析。结果慢病毒转染HFF-1最适MOI为50。PDGF处理的
HFF-1细胞表达TβRⅡ高于空白对照组(P<0.05);在PDGF作用下,转染NFI-C的HFF-1细胞表达TβRⅡ低于未转染的细胞(P<
0.05);阴性病毒无明显抑制作用(P>0.05);单纯转染NFI-C的HFF-1细胞表达TβRⅡ与空白对照组无显著性差异(P>0.05)。结
论NFI-C能抑制PDGF对TβRⅡ的上调作用,降低皮肤成纤维细胞对TGF-β的敏感性。

Abstract: Objective To investigate the effect of nuclear factor I-C (NFI-C) on platelet-derived growth factor (PDGF)-induced
up-regulation of TGF-β receptor II (TβRII) in dermal fibroblasts. Methods A lentiviral vector containing NFI-C sequence
(Lenti-GFP-NFI-C) was transfected into a human foreskin fibroblast cell line (HFF-1). Cultured HFF-1 cells, cells transfected
with Lenti-GFP-NFI-C, and cells transfected with a negative virus were stimulated with PDGF-BB, and Western blotting and
RT-qPCR were used to detect the expression levels of TβRII in the treated cells. Results PDGF treatment significantly increased
the expression level of TβRII in HFF-1 cells (P<0.05). The cells transfected with Lenti-GFP-NFI-C expressed a significantly
lower level of TβRII than non-transfected cells in response to PDGF stimulation (P<0.05), but the negative virus showed no
such inhibitory effect (P>0.05). No significant difference was found in the expression level of TβRII protein between cells
transfected with Lenti-GFP-NFI-C-transfection before PDGF stimulation and the blank control cells. Conclusion NFI-C can
inhibit PDGF-induced up-regulation of TβRII and thus reduce the sensitivity of the dermal fibroblasts to TGF-β.