期刊文献+

正常与退变髓核细胞的变形能力 被引量:3

Distortion capability of normal and degenerative nucleus pulposus cells
下载PDF
导出
摘要 背景:细胞的变形能力在较大程度上能反映出细胞结构与功能的改变,目前对髓核细胞在细胞力学方面的研究较少。目的:分析正常和退变髓核细胞的变形能力。方法:正常髓核组织和退变髓核组织分别取材于3例脊柱侧弯患者和3例椎间盘突出患者术中取出的废弃髓核组织,用胰蛋白酶和Ⅱ型胶原酶分离提取细胞,行原代培养,通过微管加载装置适宜负压下测量细胞在第4秒时吸入微管的长度,并行统计学处理。结果与结论:正常髓核细胞和退变髓核细胞所用的负压分别为(411.31±27.93)Pa,(434.24±46.26)Pa,差异有显著性意义(P<0.05)。在4s时吸入长度分别为(2.20±0.92)μm,(2.48±0.71)μm,差异无显著性意义(P>0.05)。结果可见在规定时间的情况下,吸入微管的长度基本相同时,退变髓核细胞所需要的负压较正常髓核细胞大,说明退变髓核细胞的变形能力比正常髓核细胞差。 BACKGROUND:The distortion capability of cells can reflect the changes of cell structure and function.To date,the studies on the cell mechanics of nucleus pulposus are rare.OBJECTIVE:To analyze the distortion capability of normal and degenerative nucleus pulposus in vitro.METHODS:The normal and degenerative nucleus pulposus cells were respectively obtained from discarded nucleus pulposus tissue of 3 scoliosis patients and 3 intervertebral disc hernitaion patients.Pancreatin and collagenase type Ⅱ were used to isolate the nucleus pulposus tissue and performed with primary culture.The micropipette aspiration test was used to measure the length of nucleus pulposus cells aspirated into micropipette at 4 seconds under suitable negative pressure,and the statistical analysis was performed.RESULTS AND CONCLUSION:The negative pressure of the normal and degenerative nucleus pulposus cells were(411.31±27.93) Pa and(434.24±46.26) Pa respectively,and the difference was significant(P 0.05).Within 4 seconds,the lengths of the normal and degenerative nucleus pulposus cells aspirated into micropipette were(2.20±0.92) μm and(2.48±0.71) μm,their differences were not significant(P 0.05).With the certain time and the same length of the normal and degenerative nucleus pulposus cells aspirated into micropipette,the degenerative nucleus pulposus cells needed greater negative pressure than normal nucleus pulposus cells.It indicates that the distortion capability of degenerative nucleus pulposus cells is worse than that of normal nucleus pulposus cells.
出处 《中国组织工程研究》 CAS CSCD 2012年第48期9030-9033,共4页 Chinese Journal of Tissue Engineering Research
基金 太原市中心医院科研基金项目(1120104) 项目名称:正常与退变髓核细胞拉伸 压缩试验研究~~
  • 相关文献

参考文献18

  • 1Kalichman L,Hunter DJ. The genetics of intervertebral disc degeneration.Associated genes[J].Joint Bone Spine:Revue du Rhumatisme,2008,(04):388-396.
  • 2Kaneyama S,Nishida K,Takada T. Fas ligand expression on human nucleus pulposus cel s decreases with disc degeneration processes[J].Journal of Orthopaedic Science,2008,(02):130-135.
  • 3Yang SH,Wu CC,Shih TT. In vitro study on interaction between human nucleus pulposus cel s and mesenchymal stem cel s through paracrine stimulation[J].Spine (Phila Pa 1976),2008,(18):1951-1957.
  • 4Jones P,Gardner L,Menage J. Intervertebral disc cel s as competent phagocytes in vitro:implications for cel death in disc degeneration[J].Arthritis Research &#x0026; Therapy,2008,(04):R86.
  • 5Moon SH,Nishida K,Gilbertson LG. Biologic response of human intervertebral disc cel s to gene therapy cocktail[J].Spine (Phila Pa 1976),2008,(17):1850-1855.
  • 6Pratsinis H,Kletsas D. Growth factors in intervertebral disc homeostasis[J].Connective Tissue Research,2008,(03):273-276.
  • 7Zhao CQ,Liu D,Li H. Expression of leptin and its functional receptor on disc cel s:contribution to cel proliferation[J].Spine (Phila Pa 1976),2008,(23):E858-E864.
  • 8Studer RK,Gilbertson LG,Georgescu H. p38 MAPK inhibition modulates rabbit nucleus pulposus cel response to IL-1[J].Journal of Orthopaedic Research,2008,(07):991-998.
  • 9Haefeli M,Kalberer F,Saegesser D. The course of macroscopic degeneration in the human lumbar intervertebral disc[J].Spine (Phila Pa 1976),2006,(14):1522-1531.
  • 10Cappel o R,Bird JL,Pfeiffer D. Notochordal cel produce and assemble extracel ular matrix in a distinct manner,which may be responsible for the maintenance of healthy nucleus pulposus[J].Spine (Phila Pa 1976),2006,(08):873-882.

二级参考文献19

  • 1阮狄克,何勍,丁宇,戈安星,侯黎升,李景云.颈椎间盘移植的临床研究[J].脊柱外科杂志,2003,1(1):12-14. 被引量:12
  • 2孙浩,郭超,张娟,董寅生,尹立红,林萍华,浦跃朴.骨组织工程用PLGA多孔支架的制备及细胞毒性研究[J].化工时刊,2005,19(10):1-4. 被引量:11
  • 3[1]Alini M,Li W,Markovic P,et al.The potential and limitations of a cell-seeded collagen/hyaluronan scaffold to engineer an inter-vertebral disc-like matrix[J].Spine,2003,28(5):446-454.
  • 4[2]Gries NC,Berlemann U,Moore RJ,et al.Early histolngic chan-ges in lower lumbar discs and facet joints and their correlation[J].Eur Spine J,2000,9(1):23-29.
  • 5[3]Sato M,Kiknehi M,Ishihara M,et al.Tissue engineering of the intervertebrel disc with cultured annulus fibrosus cells using atelo-collagen honeycomb-shaped scaffold with a membrane seal (ACHMS scaffold)[J].Med Biol Eng Comput,2003,41(3):365-371.
  • 6[4]Qin S,McLanghlin AP,De Vreis GW.Protection of RPE cells from oxidative injury by 15-deoxy-delta12,14-prostnglandin J2 by angmenting GSH and activating MAPK[J].Invest Ophthalmol Vis Sci,2006,47(11):5098 -5105.
  • 7[5]Yorimitsu E,Chiba K,Toyama Y,et al.Long-term ontcomes of standard discectomy for lumbar disc herniation:a follow-up study of more than 10 years[J].Spine,2001,26(6):652 -657.
  • 8[6]Loupasis GA,Stamus K,Katonis PG,et al.Seven-to 20-year ontcome of lumber disceetomy[J].Spine,1999,24(22):2313-2317.
  • 9[8]Ray CD.The PDN prosthetic disc-nucleus device[J].Eur Spine J,2002,11 Suppl 2:S137 -142.
  • 10[9]Mizuno H,Roy AK,Vacanti CA,et al.Tissue-engineered com-posites of anulus fibrosus and nucleus pulposus for intervertebral disc replacement[J].Spine,2004,29(12):1290-1297.

共引文献20

同被引文献97

引证文献3

二级引证文献39

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部