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退变颈椎椎间盘髓核中磷酸化p38 MAPK的表达 被引量:9

Expression of phosphorylated p38 MAPK in nucleus pulposus of degenerated cervical intervertebral disc
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摘要 目的观察不同退变程度颈椎病患者椎间盘髓核(nucleus pulposus,NP)的病理改变及磷酸化p38MAPK(phosphorylated p38mitogen activated protein kinase,p-p38MAPK)的表达差异,探讨颈椎椎间盘退变可能的分子机制。方法收集2008年10月至2009年5月在我院行手术治疗的35例颈椎病患者的NP组织,获取术前相应颈椎MRI(T2像正中矢状位)资料。其中男性25例,女性10例,年龄27~82岁,5例来自单间隙,18例来自两间隙,12例来自三间隙;4例为C3/4、12例为C4/5、14例为C5/6、5例为C6/7。19例NP组织用于普通病理和免疫组织化学染色,16例用于蛋白质印迹分析。采用颈椎椎间盘MRI退变分级系统评定术前NP组织标本相应MRI退变程度。观察不同退变程度时NP组织的病理改变及p-p38MAPK在NP组织中的定位;分析退变椎间盘中p-p38MAPK含量与其MRI退变程度间的关系。结果随着颈椎椎间盘退变程度加重,NP内胶原纤维逐渐增多、增粗、变性,甚至聚合成团,NP逐渐纤维化;p-p38MAPK定位于NP细胞胞核;NP细胞p-p38MAPK表达阳性率随颈椎椎间盘退变程度加重逐渐升高,不同退变等级阳性表达的程度(阴性、弱阳性、强阳性),组间差异均有统计学意义(P〈0.05);退变颈椎椎间盘中p-p38MAPK的表达量(因变量Y)与椎间盘退变程度(自变量X)间存在线性关系:Y=0.423X-0.675(P〈0.05)。结论随退变程度加重,退变NP组织中正常组织逐渐被纤维组织替代,趋于纤维化;p-p38MAPK定位于NP细胞胞核;其表达强度随退变加重而增强;p38MAPK信号通路的激活可能是人颈椎椎间盘退变的机制之一。 Objective To observe the pathological changes of nucleus pulposus(NP)in cervical spondylosis patients and the expression of phosphorylated p38 mitogen activated protein kinase(p-p38 MAPK)in NP with the progression of cervical disc degeneration,in an attempt to explore the mechanism behind cervical disc degeneration.Methods NP specimens were collected from 35 patients with cervical spondylosis,who received surgical treatment during October 2008 to May 2009 in our hospital.The preoperative MRI(T2-weighted midsagittal images)information of all patients was obtained.The 35 cases included 25 males and 10 females,with an age range of 27-82 years.Five specimens were from a single space,18 from two spaces,and 12 from three spaces;4 specimens were from C3/4,12 from C4/5,14 from C5/6,and 5 from C6/7.Nineteen specimens were used for pathology and immunohistochemistry study and 16 for Western blotting analysis.The degrees of disc degeneration were assessed by MRI grading system for cervical intervertebral disc degeneration.The pathological changes of NP of different degeneration grades and the location of p-p38 MAPK in NP were observed,and the relationship between the p-p38 MAPK and the degrees of MRI degeneration was analyzed.Results With the aggravation of discs degeneration,the collagen fibers within NP were increased,thickened,and degraded,forming clusters,and the NP gradually became fibrotic.Phosphorylated p38 MAPK located in the cell nucleus of NP tissues.The positive rate of p-p38 MAPK increased gradually with the aggravation of degeneration,and the expression degrees of p-p38 MAPK(negative,weakly positive,strongly positive)were significantly different between groups of different degeneration degrees(P0.05).A linear relationship was found between p-p38 MAPK expression and the degeneration degrees of cervical disc:Y=0.423X-0.675(P0.05).Conclusion Normal tissues are gradually replaced by fibrotic tissues in degenerated NP.Phosphorylated p38 MAPK is located in the cell nucleus of NP cells;the p-p38 MAPK plays important roles in the cervical intervertebral discs degeneration.Expression of phosphorylated p38 MAPK in NP increases with the aggravation of degeneration,suggesting that activation of p38 MAPK signaling pathway may be one of the mechanisms for cervical disc degeneration.
出处 《第二军医大学学报》 CAS CSCD 北大核心 2010年第7期739-743,共5页 Academic Journal of Second Military Medical University
基金 军队"十一五"医药卫生科研基金(06MA163)~~
关键词 颈椎病 髓核 P38丝裂原活化蛋白激酶类 椎间盘退变 cervical spondylosis nucleus pulposus p38 mitogen-activated protein kinases intervertebral disc degeneration
作者简介 [作者简介]杨志高,硕士生.Email:yangmu322301@yahoo.com.cn通讯作者(Corresponding author).Tel:021-81873396,E-mail:shenhxgk@126.com
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  • 1Borenstein D G. Epidemiology, etiology, diagnostic evaluation, and treatment of low back pain[J].Curr Opin Rheumatol, 2001,13:128 -134.
  • 2Jiang Y,Gram H,Zhao M,New L,Gu J,Feng L,et al. Characterization of the structure and function of the fourth member of p38 group mitogen-activated protein kinases, p38delta[J].J Biol Chem, 1997,272:30122-30128.
  • 3Studer R K, Gilbertson L G, Georgescu H, Sowa G, Vo N, Kang J D. p38 MAPK inhibition modulates rabbit nucleus pulposus cell response to IL-1[J].J Orthop Res, 2008,26 : 991-998.
  • 4Miyazaki M, Hong S W, Yoon S H, Morishita Y, Wang J C. Reliability of a magnetic resonance imaging based grading system for cervical intervertebral disc degeneration [J]. J Spinal Disord Tech, 2008,21 : 288-292.
  • 5Rousseau M A,Ulrich J A,Bass E C,Rodriguez A G,Liu J J, Lotz J C. Stab incision for inducing intervertebral disc degeneration in the rat[J]. Spine, 2007,32 : 17-24.
  • 6Kandel R,Roberts S,Urban J P. Tissue engineering and the in tervertebral disc : the challenges[J]. Eur Spine J, 2008,17 ( Suppl 4) :480-491.
  • 7Lurie J D, Berven S H, Gibson Chambers J, Tosteson T, Tosteson A, Hu S S, et al. Patient preferences and expectations for care: determinants in patients with lumbar intervertebral disc herniation[J].Spine, 2008,33 : 2663-2668.
  • 8顾宁,潘维,张海黔,袁春伟,韦钰,朱同银,沈家维,童明庆,周士枋.腰椎间盘中胶原的超微结构研究[J].中国医学影像技术,1995,11(6):401-404. 被引量:4
  • 9Moore R J,Vernon-Roberts B,Fraser R D,Osti O L,Schembri M. The origin and fate of herniated lumbar intervertebral disc tissue[J].Spine, 1996,21 : 2149-2155.
  • 10Brewster J L,de Valoir T,Dwyer N D,Winter E,Gustin M C. An osmosensing signal transduction pathway in yeast[J]. Science, 1993,259 :1760-1763.

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