• 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

腰椎间盘突出症组织中Fas配体的表达及椎间盘细胞凋亡

Expression of Fas ligand and apoptosis of disc cells in herniated lumbar disc tissue.

作者信息

Park J B, Chang H, Kim K W

机构信息

Department of Orthopaedic Surgery, Uijongbu St. Mary's Hospital, The Catholic University of Korea, Kyunggi-do.

出版信息

Spine (Phila Pa 1976). 2001 Mar 15;26(6):618-21. doi: 10.1097/00007632-200103150-00011.

DOI:10.1097/00007632-200103150-00011
PMID:11246372
Abstract

STUDY DESIGN

An examination of surgically obtained herniated lumbar disc tissues performed by using immunohistochemical staining and the DNA nick end labeling method.

OBJECTIVE

To investigate the cell type that expresses Fas ligand (FasL) and any evidence of apoptosis of the disc cells in herniated lumbar disc tissues.

SUMMARY OF BACKGROUND DATA

The Fas/FasL system is involved in delivering a death signal that rapidly commits the cells to apoptosis. In the authors' previous study, the expression of Fas on disc cells was identified in herniated lumbar disc tissue.

METHODS

Twenty-three herniated lumbar disc tissues (contained disc, n = 9; noncontained disc, n = 14) were examined to investigate the cell type that expresses FasL and any evidence of apoptosis of the disc cells by using immunohistochemical staining and the DNA nick end labeling method, respectively. The percentage of FasL-positive disc cells was calculated and compared with clinical and radiologic data.

RESULTS

FasL was expressed in the cytoplasm of the disc cells, and nuclear DNA fragmentation in a few disc cells was identified. A higher degree of FasL expression in disc cells was found in noncontained discs than in contained discs (P < 0.05). The percentage of FasL-positive disc cells significantly increased with the patient's age (P < 0.05), but not with the degree of disc degeneration (P > 0.05).

CONCLUSION

The current results indicate that disc cells, after herniation, undergo apoptotic cell death via autocrine or paracrine FasL mechanisms by the disc cells themselves.

摘要

研究设计

采用免疫组织化学染色和DNA缺口末端标记法对手术获取的腰椎间盘突出组织进行检查。

目的

研究腰椎间盘突出组织中表达Fas配体(FasL)的细胞类型以及椎间盘细胞凋亡的证据。

背景资料总结

Fas/FasL系统参与传递死亡信号,使细胞迅速发生凋亡。在作者之前的研究中,已在腰椎间盘突出组织中鉴定出Fas在椎间盘细胞上的表达。

方法

对23个腰椎间盘突出组织(包含椎间盘,n = 9;非包含椎间盘,n = 14)进行检查,分别采用免疫组织化学染色和DNA缺口末端标记法研究表达FasL的细胞类型以及椎间盘细胞凋亡的证据。计算FasL阳性椎间盘细胞的百分比,并与临床和放射学数据进行比较。

结果

FasL在椎间盘细胞的细胞质中表达,且在少数椎间盘细胞中鉴定出核DNA片段化。非包含椎间盘的椎间盘细胞中FasL表达程度高于包含椎间盘(P < 0.05)。FasL阳性椎间盘细胞的百分比随患者年龄显著增加(P < 0.05),但与椎间盘退变程度无关(P > 0.05)。

结论

目前的结果表明,椎间盘突出后,椎间盘细胞通过自分泌或旁分泌FasL机制自身发生凋亡性细胞死亡。

相似文献

1
Expression of Fas ligand and apoptosis of disc cells in herniated lumbar disc tissue.腰椎间盘突出症组织中Fas配体的表达及椎间盘细胞凋亡
Spine (Phila Pa 1976). 2001 Mar 15;26(6):618-21. doi: 10.1097/00007632-200103150-00011.
2
Expression of Fas receptor on disc cells in herniated lumbar disc tissue.腰椎间盘突出症组织中椎间盘细胞上Fas受体的表达
Spine (Phila Pa 1976). 2001 Jan 15;26(2):142-6. doi: 10.1097/00007632-200101150-00006.
3
The expression of Fas ligand on normal and stabbed-disc cells in a rabbit model of intervertebral disc degeneration: a possible pathogenesis.椎间盘退变兔模型中正常及针刺椎间盘细胞上Fas配体的表达:一种可能的发病机制
J Neurosurg Spine. 2007 May;6(5):425-30. doi: 10.3171/spi.2007.6.5.425.
4
Occurrence and regional distribution of apoptosis in scoliotic discs.脊柱侧弯椎间盘细胞凋亡的发生情况及区域分布
Spine (Phila Pa 1976). 2005 Mar 1;30(5):519-24. doi: 10.1097/01.brs.0000154652.96975.1f.
5
The occurrence and regional distribution of DR4 on herniated disc cells: a potential apoptosis pathway in lumbar intervertebral disc.DR4在椎间盘细胞上的发生及区域分布:腰椎间盘潜在的凋亡途径
Spine (Phila Pa 1976). 2008 Feb 15;33(4):422-7. doi: 10.1097/BRS.0b013e318163e036.
6
Nitric oxide mediates the change of proteoglycan synthesis in the human lumbar intervertebral disc in response to hydrostatic pressure.一氧化氮介导人腰椎间盘蛋白聚糖合成响应流体静压的变化。
Spine (Phila Pa 1976). 2001 Jan 15;26(2):134-41. doi: 10.1097/00007632-200101150-00005.
7
Types of lumbar herniated disc and clinical course.腰椎间盘突出症的类型及临床病程。
Spine (Phila Pa 1976). 2001 Mar 15;26(6):648-51. doi: 10.1097/00007632-200103150-00017.
8
Expression of ADAMTS-4 (aggrecanase-1) and possible involvement in regression of lumbar disc herniation.ADAMTS-4(软骨聚集蛋白聚糖酶-1)的表达及其在腰椎间盘突出症退变过程中的可能作用
Spine (Phila Pa 1976). 2006 Jun 1;31(13):1426-32. doi: 10.1097/01.brs.0000219954.67368.be.
9
Mitochondrial involvement in fas-mediated apoptosis of human lumbar disc cells.线粒体参与人腰椎间盘细胞的Fas介导的凋亡。
J Bone Joint Surg Am. 2005 Jun;87(6):1338-42. doi: 10.2106/JBJS.D.02527.
10
Herniated lumbar intervertebral discs spontaneously produce matrix metalloproteinases, nitric oxide, interleukin-6, and prostaglandin E2.腰椎间盘突出症会自发产生基质金属蛋白酶、一氧化氮、白细胞介素-6和前列腺素E2。
Spine (Phila Pa 1976). 1996 Feb 1;21(3):271-7. doi: 10.1097/00007632-199602010-00003.

引用本文的文献

1
Apoptotic Pathway in Intervertebral Disc Degeneration: From Molecular Pathways to Clinical Interventions.椎间盘退变中的凋亡途径:从分子途径到临床干预
Diagnostics (Basel). 2025 Jun 13;15(12):1510. doi: 10.3390/diagnostics15121510.
2
Unveiling the Therapeutic Potential of Baicalin in Intervertebral Disc Degeneration: Integrative Bulk and Single-Cell Transcriptome Analysis with Experimental Validation of PANoptosis Inhibition.揭示黄芩苷在椎间盘退变中的治疗潜力:基于全转录组和单细胞转录组分析并结合PAN凋亡抑制的实验验证
J Inflamm Res. 2025 May 30;18:6963-6981. doi: 10.2147/JIR.S519179. eCollection 2025.
3
Advancements in Degenerative Disc Disease Treatment: A Regenerative Medicine Approach.
退行性椎间盘疾病治疗的进展:一种再生医学方法。
Stem Cell Rev Rep. 2025 Apr 15. doi: 10.1007/s12015-025-10882-z.
4
Mechanistic insights into Guizhi Fuzi decoction for lumbar disc herniation: Integrating network pharmacology and bioinformatics approach.桂枝附子汤治疗腰椎间盘突出症的作用机制洞察:整合网络药理学与生物信息学方法
Medicine (Baltimore). 2025 Mar 21;104(12):e41917. doi: 10.1097/MD.0000000000041917.
5
Role of Embinin in the reabsorption of nucleus pulposus in lumbar disc herniation: Promotion of nucleus pulposus neovascularization and apoptosis of nucleus pulposus cells.恩宾宁在腰椎间盘突出症髓核重吸收中的作用:促进髓核新生血管形成及髓核细胞凋亡。
Open Life Sci. 2024 May 29;19(1):20220878. doi: 10.1515/biol-2022-0878. eCollection 2024.
6
Notochordal cells: A potential therapeutic option for intervertebral disc degeneration.脊索细胞:椎间盘退变的一种潜在治疗选择。
Cell Prolif. 2024 Feb;57(2):e13541. doi: 10.1111/cpr.13541. Epub 2023 Sep 11.
7
Autophagy in an extruded disc compared to the remaining disc after lumbar disc herniation in the same patient.在同一患者的腰椎间盘突出症中,比较突出的椎间盘与剩余椎间盘的自噬现象。
Eur Spine J. 2024 Jan;33(1):61-67. doi: 10.1007/s00586-023-07731-3. Epub 2023 Jun 9.
8
The role of oxidative stress in intervertebral disc cellular senescence.氧化应激在椎间盘细胞衰老中的作用。
Front Endocrinol (Lausanne). 2022 Dec 6;13:1038171. doi: 10.3389/fendo.2022.1038171. eCollection 2022.
9
Regulated cell death: Implications for intervertebral disc degeneration and therapy.程序性细胞死亡:对椎间盘退变及治疗的影响
J Orthop Translat. 2022 Nov 5;37:163-172. doi: 10.1016/j.jot.2022.10.009. eCollection 2022 Nov.
10
[Research progress of resorption of lumbar disc herniation].腰椎间盘突出症吸收的研究进展
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2022 Oct 15;36(10):1312-1316. doi: 10.7507/1002-1892.202204105.