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RhoA/ Rho激酶对类风湿关节炎患者成纤维样滑膜细胞迁移、侵袭及增殖的调控作用

[Modulation of RhoA/Rho kinase on migration, invasion and proliferation of fibroblast like synoviocytes from patients with rheumatoid arthritis].

作者信息

Liang Liu-qin, Huang Ming-cheng, Qiu Qian, Xiao You-jun, Sun Meng-ying, Zhan Zhong-ping, Ye Yu-jin, Fan Jin-jin, Yang Xiu-yan, Xu Han-shi

机构信息

Department of Rheumatology, First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2013 May 7;93(17):1345-8.

Abstract

OBJECTIVE

To evaluate the modulation of RhoA/Rho kinase (ROCK), a small Rho GTPase, on migration, invasion and proliferation of fibroblast like synoviocytes (FLS) from rheumatoid arthritis (RA) patients.

METHODS

RA FLS were collected from active RA patients. And 10% fetal bovine serum (FBS) and interleukin-1β (IL-1β) were used as stimuli in migration and proliferation experiments respectively. RhoA activity was measured by pull down assay while ROCK activity by Western blot. FLS migration and invasion in vitro were measured by the Transwell chamber method. And thiazolyl blue tetrazolium bromide (MTT) test was used to detect cell proliferation.

RESULTS

There were increased activities of RhoA and ROCK in ex vivo FLS from RA versus OA patients and healthy control. The migrated cell number of FBS-induced, C3-treated and Y27632-treated groups was 85 ± 14, 51 ± 15 and 42 ± 11 respectively. The Matrigel invading cell number of 3 groups was 64 ± 13, 39 ± 12 and 26 ± 9 respectively. Statistical differences existed in cell number between FBS-induced, C3-treated or Y27632-treated group (P < 0.05) in above migration and invasion experiments. Inhibition of RhoA and ROCK activity also suppressed the cytoskeletal reorganization and proliferation of RA FLS.

CONCLUSION

Increased RhoA/ROCK activity may contribute to abnormal migration, invasion and proliferation of RA FLS. Thus inhibition of ROCK activity may be a new therapeutic target for RA.

摘要

目的

评估小Rho GTP酶RhoA/ Rho激酶(ROCK)对类风湿关节炎(RA)患者成纤维样滑膜细胞(FLS)迁移、侵袭及增殖的调控作用。

方法

从活动期RA患者中收集FLS。在迁移和增殖实验中,分别使用10%胎牛血清(FBS)和白细胞介素-1β(IL-1β)作为刺激物。通过下拉试验测量RhoA活性,通过蛋白质免疫印迹法测量ROCK活性。采用Transwell小室法测量FLS的体外迁移和侵袭能力。使用噻唑蓝四氮唑溴盐(MTT)试验检测细胞增殖。

结果

与骨关节炎(OA)患者和健康对照相比,RA患者离体FLS中RhoA和ROCK的活性增加。FBS诱导组、C3处理组和Y27632处理组的迁移细胞数分别为85±14、51±15和42±11。3组基质胶侵袭细胞数分别为64±13、39±12和26±9。在上述迁移和侵袭实验中,FBS诱导组、C3处理组或Y27632处理组之间的细胞数存在统计学差异(P<0.05)。抑制RhoA和ROCK活性也抑制了RA FLS的细胞骨架重组和增殖。

结论

RhoA/ROCK活性增加可能导致RA FLS异常迁移、侵袭和增殖。因此,抑制ROCK活性可能是RA的一个新治疗靶点。

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