AIM: To determine the effect of pirfenidone on the activated human Müller cells by platelet-derived growth factor-BB(PDGF-BB). METHODS: The primary human Müller cells were separated from retinal tissues and ...AIM: To determine the effect of pirfenidone on the activated human Müller cells by platelet-derived growth factor-BB(PDGF-BB). METHODS: The primary human Müller cells were separated from retinal tissues and established the pathogenic model by stimulated with PDGF-BB. The Müller cells behaviour of normal group and the model group was measured by MTT assay, Trypan blue assay, cell migration assay, and collagen contraction assay. The expression of transforming growth factor(TGF)-β1,-β2, and pigment epithelium-derived factor(PEDF) was estimated with realtime polymerase chain reaction(PCR), Western blot and immunofluorescence analyses. RESULTS: A pathogenic/proliferative model of Müller cells was established by stimulating normal cultured Müller cells with 10 ng/mL PDGF-BB for 48 h. After treated with 0.2 and 0.3 mg/mL pirfenidone, the proliferation, migration and collagen contraction was statistically significantly depressed in the model group compared with the normal groups. The expression levels of TGF-β1 and TGF-β2 were significantly down-regulated, while the PEDF expression was significantly up-regulated after treated with 0.2 and 0.3 mg/mL pirfenidone in the model group. CONCLUSION: Pirfenidone effectively suppress the proliferation, migration and collagen contraction of the human Müller cells stimulated with PDGF-BB through down-regulation of TGF-β1/TGF-β2 and up-regulation of PEDF.展开更多
Background Although the migration of hepatic stellate cells （HSCs） is essential for hepatic fibrotic response, the detailed mechanisms involved are poorly understood. The aim of this study was to examine the role of...Background Although the migration of hepatic stellate cells （HSCs） is essential for hepatic fibrotic response, the detailed mechanisms involved are poorly understood. The aim of this study was to examine the role of Rho GTPases （especially RhoA） in platelet-derived growth factor （PDGF）-BB-induced migration of HSCs. Methods The migration of primary rat HSCs was evaluated using transwell Boyden chamber, while cytoskeletal changes were visualized by immunofluorescence staining of intracellular actins and vinculin. Quantitative real-time PCR and Western blotting analysis were used to detect the expression of Rho GTPases （RhoA, Racl and Cdc42） within HSCs and their activation was determined by glutathione S-transferase pull-down assay. Finally, the effects of RhoA on PDGF-BB-induced cell migration and cytoskeletal remodeling were analyzed using HSC-T6 cells stably transfected with constitutively active （CA, Q63L） or dominant negative （DN, T19N） RhoA mutants. Data were analyzed using SPSS 16.0 software. Student＇s t test was used to analyze differences between two groups and one-way analysis of variance （ANOVA） was used among multiple groups. Results Rapid cytoskeletal remodeling led to a significant increase in the motility of primary rat HSCs after haptotactic （direct） and chemotactic （indirect） stimulation by PDGF-BB： PDGF-BB caused a dramatic elevation in the levels of both total and active RhoA protein. However, the levels of mRNA for Rho GTPases, including RhoA, Racl and Cdc42, were unaffected. Furthermore, PDGF-BB induced increased formation of stress fibers and focal adhesions in HSC-T6 cells transfected with CA-RhoA, but not in HSC-T6 transfected with DN-RhoA. Surprisingly, both CA- and DN-RhoA-transfected HSC-T6 cells showed decreased migratory potential in the absence or presence of PDGF-BB compared with controls. Conclusions PDGF-BB induced cytoskeletal remodeling in rat HSCs and promoted their migration via regulation of intracellular RhoA. RhoA may be one of the determinants in PDGF-BB-induced HSC miaration.展开更多
目的观察大鼠正畸牙局部联合应用血小板衍生生长因子-BB(PDGF-BB)和转化生长因子-β1(TGF-β1)后正畸牙牙周膜中整合素β3表达的变化。方法按随机数字表法,将32只大鼠随机均分为4组。建立大鼠上颌第一磨牙近中移动正畸模型,隔日于施力...目的观察大鼠正畸牙局部联合应用血小板衍生生长因子-BB(PDGF-BB)和转化生长因子-β1(TGF-β1)后正畸牙牙周膜中整合素β3表达的变化。方法按随机数字表法,将32只大鼠随机均分为4组。建立大鼠上颌第一磨牙近中移动正畸模型,隔日于施力磨牙颊侧牙龈黏膜下分别注射1%PBS、10 ng PDGF-BB、5 ng TGF-β1、10 ng PDGF-BB和5 ng TGF-β1叠加剂量,注射体积均为0.1 mL。加力10 d后处死动物,取左上颌第一磨牙及其牙周组织,用免疫组织化学方法检测牙周组织中整合素β3的表达,进行阳性表达区域平均光密度值测量,对测量结果行方差分析,服从正态分布,再行组间t检验统计学分析。结果各实验组压力侧牙周膜细胞中整合素β3的表达强度均高于对照组(P<0.01),其中PDGF-BB+TGF-β1组与TGF-β1组或PDGF-BB组比较差异均有统计学意义(P<0.01)。实验组张力侧牙周膜细胞中整合素β3的表达强度均高于对照组(P<0.05),其中PDGF-BB+TGF-β1组整合素β3表达强度较强,与TGF-β1或PDGF-BB组比较差异无统计学意义(P>0.05)。结论局部联合应用外源性PDGF-BB和TGF-β1对大鼠正畸牙牙周组织中整合素β3的上调作用较单独运用PDGF-BB或TGF-β1组强,二者联合应用有协同效应,共同促进了正畸牙周组织改建。展开更多
文摘AIM: To determine the effect of pirfenidone on the activated human Müller cells by platelet-derived growth factor-BB(PDGF-BB). METHODS: The primary human Müller cells were separated from retinal tissues and established the pathogenic model by stimulated with PDGF-BB. The Müller cells behaviour of normal group and the model group was measured by MTT assay, Trypan blue assay, cell migration assay, and collagen contraction assay. The expression of transforming growth factor(TGF)-β1,-β2, and pigment epithelium-derived factor(PEDF) was estimated with realtime polymerase chain reaction(PCR), Western blot and immunofluorescence analyses. RESULTS: A pathogenic/proliferative model of Müller cells was established by stimulating normal cultured Müller cells with 10 ng/mL PDGF-BB for 48 h. After treated with 0.2 and 0.3 mg/mL pirfenidone, the proliferation, migration and collagen contraction was statistically significantly depressed in the model group compared with the normal groups. The expression levels of TGF-β1 and TGF-β2 were significantly down-regulated, while the PEDF expression was significantly up-regulated after treated with 0.2 and 0.3 mg/mL pirfenidone in the model group. CONCLUSION: Pirfenidone effectively suppress the proliferation, migration and collagen contraction of the human Müller cells stimulated with PDGF-BB through down-regulation of TGF-β1/TGF-β2 and up-regulation of PEDF.
基金This study was supported by a grant from the National Natural Science Foundation of China （No. 30300151 ）.
文摘Background Although the migration of hepatic stellate cells （HSCs） is essential for hepatic fibrotic response, the detailed mechanisms involved are poorly understood. The aim of this study was to examine the role of Rho GTPases （especially RhoA） in platelet-derived growth factor （PDGF）-BB-induced migration of HSCs. Methods The migration of primary rat HSCs was evaluated using transwell Boyden chamber, while cytoskeletal changes were visualized by immunofluorescence staining of intracellular actins and vinculin. Quantitative real-time PCR and Western blotting analysis were used to detect the expression of Rho GTPases （RhoA, Racl and Cdc42） within HSCs and their activation was determined by glutathione S-transferase pull-down assay. Finally, the effects of RhoA on PDGF-BB-induced cell migration and cytoskeletal remodeling were analyzed using HSC-T6 cells stably transfected with constitutively active （CA, Q63L） or dominant negative （DN, T19N） RhoA mutants. Data were analyzed using SPSS 16.0 software. Student＇s t test was used to analyze differences between two groups and one-way analysis of variance （ANOVA） was used among multiple groups. Results Rapid cytoskeletal remodeling led to a significant increase in the motility of primary rat HSCs after haptotactic （direct） and chemotactic （indirect） stimulation by PDGF-BB： PDGF-BB caused a dramatic elevation in the levels of both total and active RhoA protein. However, the levels of mRNA for Rho GTPases, including RhoA, Racl and Cdc42, were unaffected. Furthermore, PDGF-BB induced increased formation of stress fibers and focal adhesions in HSC-T6 cells transfected with CA-RhoA, but not in HSC-T6 transfected with DN-RhoA. Surprisingly, both CA- and DN-RhoA-transfected HSC-T6 cells showed decreased migratory potential in the absence or presence of PDGF-BB compared with controls. Conclusions PDGF-BB induced cytoskeletal remodeling in rat HSCs and promoted their migration via regulation of intracellular RhoA. RhoA may be one of the determinants in PDGF-BB-induced HSC miaration.
文摘目的观察大鼠正畸牙局部联合应用血小板衍生生长因子-BB(PDGF-BB)和转化生长因子-β1(TGF-β1)后正畸牙牙周膜中整合素β3表达的变化。方法按随机数字表法,将32只大鼠随机均分为4组。建立大鼠上颌第一磨牙近中移动正畸模型,隔日于施力磨牙颊侧牙龈黏膜下分别注射1%PBS、10 ng PDGF-BB、5 ng TGF-β1、10 ng PDGF-BB和5 ng TGF-β1叠加剂量,注射体积均为0.1 mL。加力10 d后处死动物,取左上颌第一磨牙及其牙周组织,用免疫组织化学方法检测牙周组织中整合素β3的表达,进行阳性表达区域平均光密度值测量,对测量结果行方差分析,服从正态分布,再行组间t检验统计学分析。结果各实验组压力侧牙周膜细胞中整合素β3的表达强度均高于对照组(P<0.01),其中PDGF-BB+TGF-β1组与TGF-β1组或PDGF-BB组比较差异均有统计学意义(P<0.01)。实验组张力侧牙周膜细胞中整合素β3的表达强度均高于对照组(P<0.05),其中PDGF-BB+TGF-β1组整合素β3表达强度较强,与TGF-β1或PDGF-BB组比较差异无统计学意义(P>0.05)。结论局部联合应用外源性PDGF-BB和TGF-β1对大鼠正畸牙牙周组织中整合素β3的上调作用较单独运用PDGF-BB或TGF-β1组强,二者联合应用有协同效应,共同促进了正畸牙周组织改建。
