期刊文献+

脂多糖刺激小鼠成骨细胞表达白细胞介素-23的实验研究 被引量:2

The in vitro study of LPS-induced IL-23 expression in murine osteoblast
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摘要 目的研究小鼠成骨细胞能否在细菌毒素产物脂多糖刺激下表达白介素-23(IL-23)。方法分别以小鼠骨髓基质干细胞(BMSCs)及小鼠成骨前体细胞系MC3T3-E1体外诱导为成骨细胞后,加以10ng/ml LPS刺激,采用ELISA法检测IL-23的蛋白表达。并采用RT-PCR方法检测脂多糖刺激下小鼠BMSCs诱导成骨细胞IL-23两亚基p19和p40 mRNA的表达。结果 10ng/ml脂多糖刺激下,小鼠BMSCs诱导成骨细胞和MC3T3-E1诱导成骨细胞均表达IL-23蛋白,BMSCs诱导成骨细胞表达IL-23两亚基p19及p40 mRNA。结论脂多糖能刺激小鼠成骨细胞表达IL-23。 Objective To examine if murine osteoblasts could express IL-23 when stimulated by lipopolysaccharide(LPS).Methods Murine bone marrow stromal cells(BMSCs) and MC3T3-E1 cells were cultured to drive osteoblasts in vitro,and stimulated by LPS.ELISA was used to test IL-23 protein expression in BMSCs and MC3T3-E1 derived osteoblasts.RT-PCR was used to examine the two chain of IL-23,p19 and p40 mRNA expression in BMSCs derived osteoblasts.Results Both BMSCs and MC3T3-E1 derived osteoblasts expressed more IL-23 protein than control(P0.05).The two chain of IL-23,p19 and p40 mRNA were expressed in BMSCs derived osteoblasts.ConclusionOsteobalst could express IL-23 when stimulated by LPS.
出处 《北京口腔医学》 CAS 2011年第3期125-127,共3页 Beijing Journal of Stomatology
基金 国家留学基金委博士后奖学金
关键词 IL-23 成骨细胞 脂多糖 IL-23 Osteoblast LPS
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参考文献15

  • 1Duey P,Schinke T,Karsenty G.The osteobalst:a sophisticated fibroblast under central surveillance.Science,2000,289(5484):1501-1504.
  • 2Teitelbaum SL Bone resorption by osteoclasts.Science,2000,289(5484):1504-1508.
  • 3Pihlstmm BL,Michalowicz BS,Johnson NW.Periodontal diseases.Lancet,2005,366(9499):1809-1820.
  • 4Schwartz Z,Goultschin J,Dean DD,et al.Mechanisms of alveolar bone destruction in periodontitis.Periodontol 2000,1997,14:158-172.
  • 5Tato CM,Cua DJ.Reconciling id,ego,and superego within interleukin-23.Immunol Rev,2008,226(1):103-111.
  • 6Hoemann CD,EI-Gabalawy H,Mckee MD.In vitro osteogenesis assays:Influenceof the primary cell source on alkaline phosphates activity and mineralization Pathol Bio (Paris),2009,57(4):318-323.
  • 7徐展望,张建新,刘亚娟,许波.体外培养骨髓基质细胞向成骨细胞的分化[J].中国组织工程研究与临床康复,2009,13(32):6295-6298. 被引量:2
  • 8王琳,刘德瑜,石心泉,裴开颜,李东,贾孟春.体外诱导小鼠骨髓基质干细胞向成骨细胞分化相关基因表达的研究[J].中华创伤骨科杂志,2006,8(11):1062-1066. 被引量:2
  • 9Tbeill L,Boyle W,Pemunger J.RANK-L and RANK:T cells,bone loss and mammalian evolution Annu Rev Immunol,2002,20:795-823.
  • 10Grecevic D,Katavic V,Lukic I,et al.Cellular and molecular interactions between immune system and bone.Croat Med J,2001,42:384-392.

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  • 1Ohyama H, Kato-Kogoe N, Kuhara A, et al. The involve- ment of IL-23 and the Thl7 pathway in periodontitis[ J]. J Dent Res, 2009, 88(7) :633 -638.
  • 2Park YD, Kim YS, Jung YM, et al. Porphyromonas gingi- valis lipopolysaccharide regulates intedeukin ( IL)- 17 and IL-23 expression via SIRT1 modulation in human periodontal ligament cells[ J]. Cytokine, 2012, 60 ( 1 ) :284 - 293.
  • 3Guo J, Yang D, Okamura H, et al. Calcium hydroxide sup- presses Porphyromonas endodontalis lipopolysaccharide-in- duced bone destruction[ J]. J Dent Res, 2014, 93(5) :508 -513.
  • 4Grivennikov SI, Wang K, Mucida D, et al. Adenoma- linked barrier defects and microbial products drive IL-23/IL- 17-mediated tumour growth [ J ]. Nature, 2012, 491 ( 7423 ) :254 - 258.
  • 5Hong CY, Lin SK, Kok SH, et al. The role of lipopolysac- charide in infectious bone resorption of periapical lesion [ J]. J Oral Pathol Med, 2004, 33(3) :162 -169.
  • 6Gaston JS, Goodall JC, Baeten D. Interleukin-23: A cen- tral cytokine in the pathogenesis of spondylarthritis[ J]. Ar- thritis Rheum, 2011, 63(12) :3668-3671.
  • 7Zhu L, Wu Y, Wei H, et al. Up-regulation of IL-23 p19 expression in human periodontal ligament fibroblasts by IL- l 13 via concurrent activation of the NF-KB and MAPKs/AP- 1 pathways [ J ]. Cytokine, 2012, 60 ( 1 ) : 171 - 178.
  • 8Martin M, Schifferle RE, Cuesta N, et al. Role of the phos- phatidylinositol 3 kinase- Akt pathway in the regulation of IL- 10 and IL-12 by Porphyromonas gingivalis lipopolysaccha- ride[J]. J Immunol, 2003, 171(2):717 -725.
  • 9Schaper K, Kietzmann M, Baumer W. Sphingosine-1-phos- phate differently regulates the cytokine production of IL-12, IL-23 and IL-27 in activated murine bone marrow derived dendritic cells[ J]. Mol Immunol, 2014, 59( 1 ) : 10 - 18.
  • 10Kuwabara T, Tanaka Y, Ishikawa F, et al. CCR7 ligands up-regulate IL-23 through PI3-kinase and NF-K B pathway in dendritic cells[J]. J Leukoc Biol, 2012, 92(2):309 - 318.

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