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兔椎间盘髓核细胞体外生物学特性的实验研究 被引量:3

EXPERIMENTAL STUDY ON BIOLOGICAL FEATURE OF RABBIT INTERVERTEBRAL DISC NUCLEUS PULPOSUS IN VITRO
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摘要 目的对兔椎间盘髓核细胞进行体外培养,观察细胞的形态、表型及超微结构改变,研究其体外生物学特性。方法取2周龄健康新西兰白兔椎间盘髓核组织,在含有15%灭活FBS的DMEM/F12培养液中培养,倒置相差显微镜下观察原代和传代细胞形态。分别在取材后、原代、第1代、第2代细胞培养期间,进行髓核细胞活力测定;爬片培养后进行甲苯胺蓝、HE、聚集蛋白聚糖番红O、Ⅰ型及Ⅱ型胶原免疫组织化学染色观察;MTT法绘制髓核细胞生长曲线,并行原代及第2代细胞透射电镜观察,对体外细胞的生物学特性进行研究。结果倒置相差显微镜见原代髓核细胞呈类圆形,折光性较强;5d开始有细胞贴壁,细胞呈多角形或短梭形;6~8d细胞生长进入指数生长期;约17d时,细胞长满瓶壁,可进行传代;随传代次数增加,细胞形态逐渐由多角形、短梭形向长梭形改变。髓核细胞活力测定在刚分离完成后细胞活力为95%~97%,原代培养期间为98%~100%,第1代培养期间仍能维持为100%,第2代细胞活力下降较为明显,为75%~80%。髓核细胞甲苯胺蓝染色呈强阳性;HE染色见细胞核、细胞质着色明显。第1代髓核细胞Ⅰ型胶原免疫组织化学染色呈阴性,Ⅱ型胶原免疫组织化学染色呈阳性,聚集蛋白聚糖番红O染色呈阳性;第2代细胞Ⅰ型胶原免疫组织化学染色呈阳性,Ⅱ型胶原免疫组织化学染色呈弱阳性,聚集蛋白多糖番红O染色着色较浅。MTT生长曲线与体外细胞培养时生长过程相符。透射电镜显示原代髓核细胞内线粒体少,胞质内有大量糖原颗粒,随传代次数增加,糖原颗粒减少,线粒体数量增多,细胞器开始肿胀。结论明确了兔髓核细胞体外生物学特性变迁,为组织工程髓核的种子细胞研究提供了实验依据。 Objective To research the biological feature of intervertebral disc nucleus pulposus cells (NPCs) by observing cell morphous, phenotype and ultramicrostructure. Methods The NPCs from 2-week-old healthy rabbit were cultured in DMEM/F 12 medium with 15% FBS. The cell biological features were observed by inverted phase contrast microscope, light microscope, electron microscope, cell vitality assay, cell growth curve and cells staining after harvest and during the periods of culturing the primary, the 1st passage and 2nd passage. Results The results of inverted phase contrast microscope showed that the primary passage adhered at 5 days, grew exponentially at 6-8 days, and were subcultured after covering the bottom at 17 days. The phenotype of the NPCs changed from polygon to long fusiform with passage increased; the vitality assay showed that there was about 95%-97%, 98%-100%, 100% and 75%-80% NPCs survived just after isolation from intervertebral disc, during the period of culturing the primary, the 1st passage and the 2nd passage, respectively. The toluidine blue staining of the NPCs was strongly positive, and HE staining showed clear cell nucleus and cytoplasm, The Ⅰ collagen immunohistochemical staining showed negative results in the 1st passage, but Ⅱ collagen immunohistochemical staining and safranin O staining showed positive results. However, the Ⅰ collagen immunohistochemical staining showed positive result in the 2nd passage, and Ⅱ collagen immunohistochemical staining and safranin O staining showed weakly positive results. The cell growth curve showed the same as the growth course of cell cultured in vitro. The results of TEM showed that there were many glycogen particles and less chondriosomes in the primary passage. With the increased passage, the glycogen particles decreased and the chondriosomes increased, and cell organ became swell. Conclusion This study clarifies the biological feature of NPCs in vitro, providing the experimental basis for the seed cell research of the nuclues pulposus tissue.
出处 《中国修复重建外科杂志》 CAS CSCD 北大核心 2008年第9期1121-1125,共5页 Chinese Journal of Reparative and Reconstructive Surgery
基金 重庆市自然科学基金资助项目(2007BB5056)~~
关键词 组织工程 髓核细胞 体外培养 生物学特性 Tissue engineering Nucleus pulposus cells Culture in vitro Biological feature Rabbit
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参考文献22

  • 1胡有谷.腰椎间盘突出症.2版.北京:人民卫生出版社,1995.
  • 2孟壮志,朱青安,范真,赵卫东,欧阳钧,钟世镇.腰骶部椎间盘髓核摘除对脊柱稳定性影响的生物力学研究[J].中国临床解剖学杂志,1999,17(1):75-76. 被引量:33
  • 3Roughleya P, Hoemann C, DesRosiers E, et al. The potential of chitosan-based gels containing intervertebral disc cells for nucleus pulposus supplementation. Biomaterials, 2006, 27(3): 388-396.
  • 4Anderson DG, Risbud MV, Shapiro IM, et al. Cell-based therapy for disc repair. Spine J, 2005, 5(6 Suppl): 297S-303S.
  • 5Sobajima S, Vadala G, Shimer A, et al. Feasibility of a stem cell therapy for intervertebral disc degeneration. Spine ], 2007. [Epub ahead of print]
  • 6Gruber HE, Hanley EN Jr. Recent advances in disc cell biology. Spine, 2003, 28(2): 186-193.
  • 7Roughley PJ,Alini M, Antoniou J. The role of proteoglycans in aging, degeneration and repair of the intervertebral disc. Biochem Soc Trans, 2002, 30(Pt 6): 869-874.
  • 8Gan JC, Ducheyne P, Vresilovic E, et al. Bioactive glass serves as a substrate for maintenance of phenotype of nucleus pulposus cells of the intervertebral disc. J Biomed Mater Res, 2000, 51(4): 596-604.
  • 9张传志,周跃,李长青.兔髓核细胞体外最佳培养条件的探索[J].中国矫形外科杂志,2005,13(14):1093-1096. 被引量:22
  • 10Gan JC, Ducheyne P, Vresilovic EJ, et al. Intervertebral disc tissue engineering Ⅱ cultures of nucleus pulposus cells. Clin Orthop Relat Res, 2003, (411): 315-324.

二级参考文献29

共引文献105

同被引文献34

  • 1王文波,赵勇,卢宇,李雪松,赵哲,于长水.骨形态发生蛋白-2对椎间盘细胞软骨特异性基因mRNA的调节作用[J].中华实验外科杂志,2005,22(6):719-721. 被引量:2
  • 2Walker BF.The prevalence of low back pain:a systematic review of the literature from 1966 to 1998[J].J Spinal Disord,2000,13:205-217.
  • 3Amit A,Sachin G,Makarand VR,et al.Cited2Modulates Hypoxia-In-ducible Factor-Dependent Expression of Vascular Endothelial Growth Factor in Nucleus Pulposus Cells of the Rat Intervertebral Disc[J].Arthritis rheumatism,2008,58(12):3798-3808.
  • 4Yan Z,Keith GD,Makarand VR,et al.HIF-1alpha is a regulator of ga-lectin-3expression in the intervertebral disc[J].J Bone Miner Res,2007,22(12):1851-1861.
  • 5Makarand VR,Asha G,Irving MS,et al.Nucleus pulposus cells expre-ss HIF-1alpha under normoxic culture conditions:A metabolic adapta-tion to the intervertebral disc microenvironment[J].J Cell Biochem,2006,98:152-159.
  • 6Renata S,Dessislava M,Makarand VR,et al.Hypoxia-Inducible Fact-or Regulation of ANK Expression in Nucleus Pulposus Cells[J].Arthr-itis rheumatism,2010,62(9):2707-2715.
  • 7Song C,Sanford EE,Ming P.Coculture of synovium-derived stem cel-ls and nucleus pulposus cells in serum-free defined medium with supp-lementation of transforming growth factor-beta1:a potential applicati-on of tissue-specific stem cells in disc regeneration[J].Spine(Phila Pa 1976),2009,34(12):1272-1280.
  • 8Akihiko H,Daisuke S,Joji M,et al.Enhancement of Intervertebral Disc Cell Senescence by WNT/-Catenin Signaling-Induced Matrix Metalloproteinase Expression[J].Arthritis&Rheumatism,2010,62(10):3036-3047.
  • 9Maitre CL,Pockert A,Hoyland JA,et al.Matrix synthesis and degrad-ation in human intervertebral disc degeneration[J].Biochem Soc Tra-ns,2007,35(4):652-655.
  • 10Ha KY,Koh IJ,Han CW,et al.The expression of hypoxia inducible factor-1alpha and apoptosis in herniated discs[J].Spine(Phila Pa1976),2006,31(12):1309-1313.

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