• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

正常和脊柱侧弯的人类椎间盘内X型胶原蛋白表达模式随年龄的变化

Variation with age in the pattern of type X collagen expression in normal and scoliotic human intervertebral discs.

作者信息

Aigner T, Gresk-otter K R, Fairbank J C, von der Mark K, Urban J P

机构信息

Department of Pathology, Friedrich-Alexander-University of Erlangen, Nurnberg, FRG.

出版信息

Calcif Tissue Int. 1998 Sep;63(3):263-8. doi: 10.1007/s002239900524.

DOI:10.1007/s002239900524
PMID:9701632
Abstract

The distribution and expression of type X collagen, a calcium-binding collagen, which is a marker of hypertrophic chondrocytes and thought to be involved in cartilage calcification, was examined in situ in nondegenerate (grade I or II) human discs taken at autopsy over a wide age range (fetal->80 years) and also in scoliotic discs removed at surgery. In the fetal vertebral column, type X collagen was strongly expressed in the hypertrophic chondrocytes of the endplate, but was not seen in other areas. In the cartilaginous endplate of adults, it was found over the whole age range examined, with intensity increasing with age. In the disc matrix itself, type X collagen was demonstrated around individual cells from all individuals older than 50 years, but not in any fetal or autopsy disc from individuals younger than 40 years. In scoliotic discs, however, focal type X collagen expression was seen in 3/8 patients younger than 40 years including one 12-year-old. No type X collagen was found in the outer annulus in any autopsy or scoliotic disc, supporting the idea that cells of the outer annulus are phenotypically distinct from cells of the inner annulus and the nucleus. Our results demonstrate for the first time that type X collagen is a possible gene product of the intervertebral disc cells and a potential biochemical component of the disc matrix. They indicate that with age or in scoliosis, some cells from the inner annulus or nucleus of the disc differentiate to the hypertrophic chondrocyte phenotype. This might be the initiating event for the abnormal calcification described in aged and scoliotic discs in other studies.

摘要

X型胶原是一种钙结合胶原,是肥大软骨细胞的标志物,被认为参与软骨钙化。我们对取自不同年龄(胎儿至80岁)尸体解剖的非退变(I级或II级)人类椎间盘以及手术切除的脊柱侧弯椎间盘进行了X型胶原分布和表达的原位检测。在胎儿脊柱中,X型胶原在终板的肥大软骨细胞中强烈表达,但在其他区域未见表达。在成人的软骨终板中,在整个检测年龄范围内均有发现,且强度随年龄增加。在椎间盘基质本身,X型胶原在所有50岁以上个体的单个细胞周围均有显示,但在40岁以下个体的任何胎儿或尸体解剖椎间盘中均未发现。然而,在脊柱侧弯椎间盘中,在3/8例40岁以下患者中观察到局灶性X型胶原表达,其中包括一名12岁患者。在任何尸体解剖或脊柱侧弯椎间盘中,在外环均未发现X型胶原,这支持了外环细胞在表型上与内环和髓核细胞不同的观点。我们的结果首次表明,X型胶原是椎间盘细胞可能的基因产物和椎间盘基质的潜在生化成分。结果表明,随着年龄增长或在脊柱侧弯情况下,椎间盘内环或髓核的一些细胞会分化为肥大软骨细胞表型。这可能是其他研究中描述的老年和脊柱侧弯椎间盘异常钙化的起始事件。

相似文献

1
Variation with age in the pattern of type X collagen expression in normal and scoliotic human intervertebral discs.正常和脊柱侧弯的人类椎间盘内X型胶原蛋白表达模式随年龄的变化
Calcif Tissue Int. 1998 Sep;63(3):263-8. doi: 10.1007/s002239900524.
2
Elevated synthetic activity in the convex side of scoliotic intervertebral discs and endplates compared with normal tissues.与正常组织相比,脊柱侧弯椎间盘和终板凸侧的合成活性升高。
Spine (Phila Pa 1976). 2001 May 15;26(10):E198-206. doi: 10.1097/00007632-200105150-00002.
3
[Primary study on collagen X gene expression in the apical disc of idiopathic scoliosis].[特发性脊柱侧凸顶椎椎间盘胶原X基因表达的初步研究]
Zhonghua Yi Xue Za Zhi. 2004 Oct 17;84(20):1681-5.
4
1997 Volvo Award winner in basic science studies. Immunohistologic markers for age-related changes of human lumbar intervertebral discs.1997年沃尔沃基础科学研究奖获得者。人类腰椎间盘退变的免疫组织学标志物。
Spine (Phila Pa 1976). 1997 Dec 15;22(24):2781-95. doi: 10.1097/00007632-199712150-00001.
5
Changes in collagen cross-linking in degenerative disc disease and scoliosis.退行性椎间盘疾病和脊柱侧弯中胶原蛋白交联的变化。
Spine (Phila Pa 1976). 1998 Dec 1;23(23):2545-51. doi: 10.1097/00007632-199812010-00009.
6
Immunolocalization of type X collagen in human lumbar intervertebral discs during ageing and degeneration.衰老和退变过程中人类腰椎间盘X型胶原蛋白的免疫定位
Histochem Cell Biol. 1997 Dec;108(6):471-80. doi: 10.1007/s004180050187.
7
Ultrastructural localization and distribution of proteoglycan in normal and scoliotic lumbar disc.蛋白聚糖在正常和脊柱侧弯腰椎间盘的超微结构定位与分布
Spine (Phila Pa 1976). 2005 Jun 1;30(11):1303-9. doi: 10.1097/01.brs.0000164284.17039.65.
8
[The expression of collagen IX in the apical disc of idiopathic scoliosis].[胶原蛋白IX在特发性脊柱侧凸顶椎椎间盘的表达]
Zhonghua Wai Ke Za Zhi. 2005 Apr 15;43(8):513-6.
9
Phenotypic characteristics of rabbit intervertebral disc cells. Comparison with cartilage cells from the same animals.兔椎间盘细胞的表型特征。与同一动物的软骨细胞的比较。
Spine (Phila Pa 1976). 1999 May 1;24(9):837-44. doi: 10.1097/00007632-199905010-00002.
10
Calcification in human intervertebral disc degeneration and scoliosis.人类椎间盘退变和脊柱侧凸中的钙化。
J Orthop Res. 2011 Dec;29(12):1888-95. doi: 10.1002/jor.21456. Epub 2011 May 16.

引用本文的文献

1
Cellular senescence and other age-related mechanisms in skeletal diseases.骨骼疾病中的细胞衰老及其他与年龄相关的机制。
Bone Res. 2025 Jul 7;13(1):68. doi: 10.1038/s41413-025-00448-7.
2
TNF induces catabolism in human cartilaginous endplate cells in 3D agarose culture under dynamic compression.肿瘤坏死因子(TNF)在动态压缩下的三维琼脂糖培养中诱导人软骨终板细胞发生分解代谢。
Sci Rep. 2025 May 6;15(1):15849. doi: 10.1038/s41598-025-00538-w.
3
Qualitative and Quantitative MR Imaging of the Cartilaginous Endplate: A Review.软骨终板的定性和定量磁共振成像:综述
J Magn Reson Imaging. 2025 Apr;61(4):1552-1571. doi: 10.1002/jmri.29562. Epub 2024 Aug 20.
4
Cartilaginous endplates: A comprehensive review on a neglected structure in intervertebral disc research.软骨终板:对椎间盘研究中一个被忽视结构的全面综述。
JOR Spine. 2023 Oct 21;6(4):e1294. doi: 10.1002/jsp2.1294. eCollection 2023 Dec.
5
Morphological alterations of lumbar intervertebral discs in patients with adolescent idiopathic scoliosis.青少年特发性脊柱侧凸患者腰椎间盘的形态学改变。
Spine J. 2024 Jan;24(1):172-184. doi: 10.1016/j.spinee.2023.08.012. Epub 2023 Aug 21.
6
Multiple nano-drug delivery systems for intervertebral disc degeneration: Current status and future perspectives.用于椎间盘退变的多种纳米药物递送系统:现状与未来展望。
Bioact Mater. 2022 Nov 20;23:274-299. doi: 10.1016/j.bioactmat.2022.11.006. eCollection 2023 May.
7
Suppression of Sost/Sclerostin and Dickkopf-1 Augment Intervertebral Disc Structure in Mice.抑制Sost/硬骨素和Dickkopf-1可增强小鼠椎间盘结构。
J Bone Miner Res. 2022 Jun;37(6):1156-1169. doi: 10.1002/jbmr.4546. Epub 2022 Apr 20.
8
Tea Polyphenol Attenuates Oxidative Stress-Induced Degeneration of Intervertebral Discs by Regulating the Keap1/Nrf2/ARE Pathway.茶多酚通过调节 Keap1/Nrf2/ARE 通路减轻氧化应激诱导的椎间盘退变。
Oxid Med Cell Longev. 2021 Jan 7;2021:6684147. doi: 10.1155/2021/6684147. eCollection 2021.
9
Characterization of bovine and canine animal model cartilage endplates and comparison to human cartilage endplate structure, matrix composition, and cell phenotype.牛和犬动物模型软骨终板的特征及其与人类软骨终板结构、基质组成和细胞表型的比较。
JOR Spine. 2020 Aug 12;3(4):e1116. doi: 10.1002/jsp2.1116. eCollection 2020 Dec.
10
Injectable ECM hydrogel for delivery of BMSCs enabled full-thickness meniscus repair in an orthotopic rat model.用于递送骨髓间充质干细胞的可注射细胞外基质水凝胶能够在原位大鼠模型中实现全层半月板修复。
Bioact Mater. 2020 Jun 30;5(4):871-879. doi: 10.1016/j.bioactmat.2020.06.008. eCollection 2020 Dec.