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不同浓度SDF1、bFGF、IL-8对骨髓间充质干细胞的趋化作用 被引量:2

Comparison of chemotaxis of different concentrations of SDF1,b FGF,IL-8 on bone marrow mesenchymal stem cell
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摘要 目的:研究比较不同趋化因子[骨髓基质细胞衍生因子1(stromal cell-derived factor-1,SDF-1)、碱性成纤维细胞生长因子(basic fibroblast growth factor,b FGF)和白介素8(interleukin-8,IL-8)]在多个浓度下对骨髓间充质干细胞(bone marrow mesenchymal stem cells,BMSCs)的趋化作用。方法:实验分为3组,即SDF1组、b FGF组、IL-8组,每组因子浓度为0(对照浓度)、10、50、100、200、400 ng/m L(实验浓度)。抽取SD大鼠骨髓,分离培养BMSCs,利用Transwell小室研究不同浓度SDF1、b FGF、IL-8对BMSCs的趋化作用,获得3种因子趋化BMSCs的最佳浓度。采用SPSS16.0软件包对数据进行统计学分析。结果:与0 ng/m L(对照浓度)组相比,3种因子均可趋化BMSCs(P<0.05);50、100、400 ng/m L浓度下,SDF1对BMSCs的趋化作用显著高于b FGF(P<0.05);200 ng/m L浓度下,SDF1对BMSCs的趋化作用强于IL-8;SDF1及IL-8对BMSCc趋化作用的最佳浓度均为100 ng/m L,b FGF的最佳浓度为200 ng/m L。结论:SDF-1、b FGF、IL-8均可趋化BMSCs,SDF-1与IL-8的趋化效果更佳。 PURPOSE: To investigate chemotaxis of different concentrations of chemokines stromal cell-derived factor-1 (SDF-1), basic fibroblast growth factor (bFGF) and interleukin-8 (IL-8)on bone marrow mesenchymal stem cells (BMSCs). METHODS: The experiment group was divided into 3 groups according to different culture media: SDF1, bFGF and IL-8. The chemokine concentrations of each group was 0 ng/mL (control concentration), 10 ng/mL, 50 ng/mL, 100 ng/mL, 200ng/ mL and 400 ng/mL (experimental concentration). BMSCs were isolated from SD rats and cultured in vitro. 24-well plates with an 8 μm pore size polycarbonate membrane were used to examine the chemotaxis of SDF1, bFGF, IL-8 on BMSCs, respectively, and to obtain the best chemotactic concentrations of 3 chemokines. The data was analyzed with SPSS 16.0 software package. RESULTS: Compared with 0 ng/mL group, all chemokines could ehemoattract BMSCs (P〈0.05). At the concentration of 50 ng/mL, 100 ng/mL and 400 ng/mL, SDF1 significantly recruited more cells than bFGF (P〈O.05); SDF1 significantly recruited more cells than IL-8 at the concentration of 200 ng/mL; The best chemotaetie concentration was 100 ng/mL for SDF1 and IL-8 and 200 ng/mL for bFGF. CONCLUSIONS: The use of SDFI,bFGF,IL-8 can ehemoattraet BMSCs. The ehemotaxis of SDF1 and IL-8 are better than bFGF.
出处 《上海口腔医学》 CAS CSCD 2015年第3期275-279,共5页 Shanghai Journal of Stomatology
基金 上海市科学技术委员会医学引导项目(124119b0101)~~
关键词 SDF1 b FGF IL-8 骨髓间充质干细胞 趋化作用 SDF1 BFGF IL-8 BMSCs Chemotaxis
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参考文献19

  • 1Jones GN, Moschidou D, Lay K, et al. Upregulating CXCR4 in human fetal mesenchymal stem ceils enhances engraftment and bone mechanics in a mouse model of osteogenesis imperfecta [J].Stem Cells Transl Med, 2011, 1(1): 70-78.
  • 2Doerks T, Copley RR, Schultz J, et al. Systematic identification of novel protein domain fami/ies associated with nuclear functions [J]. Genome Res, 2002, 12(1): 47-56.
  • 3Cui X, Chopp M, Zacharek A, et al. Chemokine, vascular and therapeutic effects of combination Simvastatin and BMSC treatment of stroke [J]. Neurobiol Dis, 2009, 36(1): 35-41.
  • 4Theiss HD, Vallaster M, Rischpler C, et al. Dual stem cell therapy after myocardial infarction acts specifically by enhanced homing via the SDF-1/CXCR4 axis[J]. Stem Cell Res, 2011, 7(3): 244-255.
  • 5Ghadge SK, Mtihlstedt S, Ozcelik C, et al. SDF-loL as a therapeutic stem cell homing factor in myocardial infarction [J]. Pharmacol Ther, 2011, 129(1): 97 - 108.
  • 6Lau TI?, Wang DA. Stromal cell-derived factor-1 (SDF-1): homing factor for engineered regenerative medicine [J]. Expert Opin Biol Ther, 2011, 11(2): 189-197.
  • 7Kitaori T, Ito H, Schwarz EM, et al. Stmmal cell-derived factor 1/CXCR4 signaling is critical for the recruitment of mesenchymal stem cells to the fracture site during skeletal repair in a mouse model H1. Arthritis Rheum 2009., 60(3):-813-823 .
  • 8Carr AN, Howard BW, Yang HT, et al. Efficacy of systemic administration of SDF-1 in a model of vascular insufficiency: support for an endothelium-dependent mechanism [J].Cardiovasc Res, 2006, 69(4): 925-935.
  • 9Kerfoot SM, Andonegui G, Bonder CS, et al. Exogenous stromal cell-derived factor-1 induces modest leukocyte recruitment in vivo [J]. Am J Physiol Heart Circ Physiol, 2008, 294(6): H2524-2534.
  • 10Tasso R, Gaetani M, Molino E, et al. The role of bFGF on the ability of MSC to activate endogenous regenerative mechanisms in an eetopic bone formation model [J]. Biomaterials, 2012, 33(7): 2086-2096.

二级参考文献9

  • 1Luan Q X,J Gifu Dent Soc,1999年,26卷,291页
  • 2Kapila Y L,J Periodontol,1998年,69卷,1008页
  • 3Nishimura F,J Dent Res,1996年,75卷,986页
  • 4Dunlevy J R,J Cell Sci,1995年,108卷,1期,311页
  • 5Yue T L,Eur J Pharmacol,1993年,240卷,81页
  • 6Michel G,FEBS Lett,1992年,305卷,241页
  • 7Somerman M J,J Periodontol,1989年,60卷,73页
  • 8Somerman M J,J Dent Res,1988年,67卷,66页
  • 9Baggiolini M,Prog Biochem Pharmacol,1988年,22卷,90页

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