Li Lei, Jiang Wei, Wang Ji-yao, Yang Chang-qing
Department of Gastroenterology, Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Zhonghua Gan Zang Bing Za Zhi. 2010 Aug;18(8):581-4. doi: 10.3760/cma.j.issn.1007-3418.2010.08.008.
To evaluate the effects of collagens and growth factors TGFß1 and PDGF-BB on the cytoskeletal components and migration in cultured rat hepatic stellate cells (HSCs).
Primary rat hepatic stellate cells were isolated and cultured. A Transwell Chamber system was used to observe the changes of serum starved HSCs haptotactic migration (direct stimulation) and chemotactic migration (indirect stimulation) after collagens and growth factors treatment. Changes in actin cytoskeletal organization were visualized by fluorescence staining using FITC-labeled phalloidin and the fluorescence images were recorded using confocal microscopy.
TGFß1 enhanced significantly the motility of primary HSCs at 5 ng/ml: for haptotactic migration cells: 131.37+/-3.15 vs 102.93+/-1.01, F=40.84, P<0.05; for chemotactic migration cells: 210.17+/-1.78 vs 102.93+/-1.01, F=64.53, P<0.05. PDGF-BB enhanced significantly the motility of primary HSCs at 10 ng/ml (haptotactic migration cells: 203.67+/-7.54 vs 102.93+/-1.01, F=40.90, P<0.05; chemotactic migration cells: 319.56+/-11.71 vs 102.93+/-1.01, F=54.57, P<0.05); Both chemotactic and haptotactic stimuli with 100 microg/ml collagen type I significantly increased HSCs migration: for haptotactic migration cells: 127.20+/-6.47 VS 102.93+/-1.01, F=41.01, P is less than 0.05; for chemotactic migration cells: 201.52+/-11.28 vs 102.93+/-1.01, F=36.49, P<0.05; however, collagen type IV had no effect on HSCs migration. Serum-starved, untreated cells had a rounded-up morphology. PDGF-BB and TGFß1 induced a rapid morphological change concomitant with a robust reorganization of actin cytoskeleton in HSCs.
Collagen type I, PDGF-BB and TGFß1 could induce cell migration in HSCs, but collagen type IV has no such effect. PDGF-BB and TGFß1 could induce the actin cytoskeleton reorganization in HSCs.
评估胶原蛋白以及生长因子转化生长因子β1(TGFβ1)和血小板衍生生长因子BB(PDGF - BB)对培养的大鼠肝星状细胞(HSCs)细胞骨架成分及迁移的影响。
分离并培养原代大鼠肝星状细胞。使用Transwell小室系统观察胶原蛋白和生长因子处理后血清饥饿的HSCs的趋触性迁移(直接刺激)和趋化性迁移(间接刺激)的变化。使用异硫氰酸荧光素(FITC)标记的鬼笔环肽通过荧光染色观察肌动蛋白细胞骨架组织的变化,并用共聚焦显微镜记录荧光图像。
TGFβ1在5 ng/ml时显著增强原代HSCs的运动性:趋触性迁移细胞:131.37±3.15对102.93±1.01,F = 40.84,P<0.05;趋化性迁移细胞:210.17±1.78对102.93±1.01,F = 64.53,P<0.05。PDGF - BB在10 ng/ml时显著增强原代HSCs的运动性(趋触性迁移细胞:203.67±7.54对102.93±1.01,F = 40.90,P<0.05;趋化性迁移细胞:319.56±11.71对102.93±1.01,F = 54.57,P<0.05);100 μg/mlⅠ型胶原蛋白的趋化性和趋触性刺激均显著增加HSCs迁移:趋触性迁移细胞:127.20±6.47对102.93±1.01,F = 41.01,P<0.05;趋化性迁移细胞:201.52±11.28对102.93±1.01,F = 36.49,P<0.05;然而,Ⅳ型胶原蛋白对HSCs迁移无影响。血清饥饿的未处理细胞呈圆形。PDGF - BB和TGFβ1诱导HSCs快速发生形态变化,同时伴随肌动蛋白细胞骨架的强烈重组。
Ⅰ型胶原蛋白、PDGF - BB和TGFβ1可诱导HSCs细胞迁移,但Ⅳ型胶原蛋白无此作用。PDGF - BB和TGFβ1可诱导HSCs中肌动蛋白细胞骨架重组。