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A型核纤层蛋白在腰椎退行性疾病中的表达及其意义 被引量:1

Expression and significance of type A lamin in lumbar spinal degenerative disease
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摘要 目的初步探讨A型核纤层蛋白(Lamin A)在腰椎退行性疾病中的表达特点及意义。方法将74例腰椎退行性疾病患者分为腰椎间盘突出组(32例)及腰椎管狭窄组(42例),另设腰椎正常组(12例)作为对照。采用免疫组织化学检查(免疫组化)及蛋白免疫印迹法检测Lamin A在3组腰椎间盘组织标本中的表达情况。结果免疫组化显示Lamin A在3组的椎间盘细胞中均有表达,腰椎管狭窄组的Lamin A在椎间盘细胞中的表达较腰椎正常组及腰椎间盘突出组明显;蛋白免疫印迹法检测3组椎间盘的纤维环组织均有Lamin A的表达,腰椎管狭窄组Lamin A条带灰度值为3.55±0.16,腰椎间盘突出组为1.02±0.13,腰椎正常组为0.78±0.14,3组比较差异有统计学意义(F=14.326,P<0.01),腰椎管狭窄组与腰椎间盘突出组及腰椎正常组比较差异均有统计学意义(P均<0.001),腰椎间盘突出组与腰椎正常组比较差异尚未有统计学意义(P=0.134)。结论随着腰椎退行性疾病病程的发展,Lamin A的表达逐渐升高,其可能与腰椎退行性疾病的发生、发展有一定联系。 Objective To preliminarily explore the expression levels and clinical significance of type A lamin (lamin A)in lumbar spinal degenerative disease.Methods Seventy four patients diagnosed with lumbar spinal degenerative disease were divided into the lumbar disc herniation (n =32)and lumbar spinal stenosis groups (n =42)and healthy subjects were recruited into the control group (n =12).The expression of lamin A in the lumbar tissue samples from three groups was assessed by immunohistochemical examination and western blotting.Results Immunohistochemical analysis revealed that lamin A was expressed in the interver-tebral disk cells from all three groups.The staining of lamin A in the tissue from lumbar spinal stenosis group was stronger than those from the other two groups.Western blot demonstrated that lamin A was expressed in the fibrous ring tissue of intervertebral disk from all three groups.In the lumbar spinal stenosis group,the expres-sion level of lamin A was 3.55 ±0.16(gray level),1.02 ±0.13 in the lumbar disc herniation group and 0.78 ± 0.14 in the control group with statistical significance among three groups (F =14.326,P 〈0.01).Statistical significance was noted between the lumbar spinal stenosis and lumbar disc herniation group /the control group (both P 〈0.001).There was no statistically significant difference between the lumbar disc herniation and con-trol groups (P =0.134).Conclusions Over the progression of degenerative lumbar spinal disease,the ex-pression level of lamin A is gradually up-regulated,which is probably associated with the incidence and devel-opment of degenerative lumbar spinal disease.
出处 《新医学》 2015年第11期724-727,共4页 Journal of New Medicine
基金 广东省科技计划项目(2012B040304006) 2012年广东省大学生创新创业训练计划项目(1057112012)
关键词 A型核纤层蛋白 腰椎间盘突出 腰椎管狭窄 表达 Type A lamin Lumbar disc herniation Lumbar spinal stenosis Expression
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参考文献15

  • 1Sch:ipe J, Prausse S, Radmacher M, Stick R. Influence of lamin A on the mechanical properties of amphibian o- ocyte nuclei measured by atomic force microscopy. Bio- phys J, 2009, 96 (10): 4319-4325.
  • 2Funkhouser CM, Sknepnek R, Shimi T, Goldman AE, Goldman RD, Olvera de la Cruz M. Mechanical model of blebbing in nuclear lamin meshworks. Proc Natl Acad Sci U S A, 2013, 110 (9) : 3248-3253.
  • 3Espada J, Varela I, Flores I, Ugalde AP, Cadi anos J, Pend6s AM, Stewart CL, Tryggvason K, Blasco MA, Freije JM, L6pez-Ot:n C. Nuclear envelope defects cause stem cell dysfunction in premature-aging mice. J Cell Biol, 2008, 181 (1) : 27-35.
  • 4Sive JI, Baird P, Jeziorsk M, Watkins A, Hoyland JA, Freemont AJ. Expression of chondrocyte markers by cells of normal and degenerate intervertebral discs. Mol Pathol, 2002, 55 (2): 91-97.
  • 5Zhang YG, Zhang F, Sun Z, Guo W, Liu J, Liu M, Guo X. A controlled case study of the relationship be- tween environmental risk factors and apoptotic gene poly-morphism and lumbar disc 2013, 182 (1) : 56-63.
  • 6Sun Z, Ling M, Chang Y, herniation. Am J Pathol, Huo Y, Yang G, Ji Y, Li Y. Single-nucleotide gene.polymorphisms involving cell death pathways : a study of Chinese patients with lumbar disc herniation. Connect tissue Res, 2013, 54 (1) : 55-61.
  • 7范东伟,陈仲强,郭昭庆,齐强,李危石.周期性牵张应力对人椎间盘纤维环细胞合成和分解的影响[J].天津医药,2014,42(3):241-244. 被引量:6
  • 8Swift J, Ivanovska IL, Buxboim A, Harada T, Dingal PC, Pinter J, Pajerowski JD, Spinler KR, Shin JW, Tewari M, Rehfeldt F, Speicher DW, Discher DE. Nu- clear lamin-A scales with tissue stiffness and enhances matrix-directed differentiation. Science, 2013, 341 (6149) : 1240104.
  • 9Engler A J, Sen S, Sweeney HL, Discher DE. Matrix e- lasticity directs stem cell lineage specification. Cell, 2006, 126 (4): 677-689.
  • 10Duque G, Rivas D. Age-related changes in lamin A/C expression in the osteoarticular system: laminopathies as a potential new aging mechanism. Mech Ageing Dev, 2006, 127 (4): 378-383.

二级参考文献25

  • 1赛佳明,胡有谷,王德春.椎间盘髓核细胞组织块法原代培养[J].脊柱外科杂志,2006,4(5):315-316. 被引量:10
  • 2吴在德 吴肇汉.外科学[M]6版[M].北京:人民卫生出版社,2003.267-268.
  • 3AGRAWAL A, GAJGHATE S, SMITH H, et al. Cited2 modulates hypoxia-inducible factor-dependent expression of vascular endothelial growth factor in nucleus pulposus cells of the rat intervertebral disc [ J ]. Arthritis Rheum, 2008, 58 (12) : 3798-3808.
  • 4Buckwalter J A. Aging and degeneration of the human intervertebral disc[J]. Spine, 1995, 20 (11): 1307- 1314.
  • 5HUTI'ON W C, ADAMS M A. The biomechanics of disc degeneration[J]. Acta Orthop Belg, 1987, 53 (2) : 143 -147.
  • 6GRUBER H E, STASKY A A, HANLEY EN J R. Characterization and phenotypic stability of human disc cels in vitrn[]. Matrix Biol, 1997, 16 (5) : 285-288.
  • 7GRUBER H E, FISHER EC, J R. , DESAI B, et al. Human intervertebral disc cells from the annulus: three- dimensional culture in agarose or alginate and respon- siveness to TGF-betal [J]. Exp Cell Res, 1997, 235 (1): 13-21.
  • 8WANG F, WU X T, ZHUANG S Y, et al. Ex vivo ob- servation of human nucleus pulposus chondrocytes isola- ted from degenerated intervertebral discs [ J ]. Asian Spine J, 2011, 5 (2): 73-81.
  • 9HUTTON W C, ELMER W A, BRYCE L M, et al. Do the intervertebral disc cells respond to different levels of hydrostatic pressure? [J]. Clin Biomech (Bristol, Avon) , 2001, 16 (9): 728-734.
  • 10RAZAQ S, WILKINS R J, URBAN J P. The effect of extracellular pH on matrix turnover by cells of the bovine nucleus pulposus [ J ]. European Spine Journal, 2003, 12 (4): 341-349.

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