• 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

成年人类关节软骨中的间充质祖细胞。

Mesenchymal progenitor cells in adult human articular cartilage.

作者信息

Hiraoka Koji, Grogan Shawn, Olee Tsaiwei, Lotz Martin

机构信息

Division of Arthritis Research, The Scripps Research Institute, La Jolla, CA 92037, USA.

出版信息

Biorheology. 2006;43(3,4):447-54.

PMID:16912416
Abstract

The transmembrane receptor Notch-1 regulates cell fate and differentiation and was suggested to identify a cell type with progenitor characteristics in newborn bovine articular cartilage. We show that Notch-1 is expressed on > 70% of BM-MSC in early passage monolayer culture. We also demonstrate that normal articular cartilage contains Notch-1+ cells and that the frequency is increased in OA. Most Notch-1+ cells in OA cartilage are located in the clusters of proliferating cells. These findings indicate that multipotential mesenchymal progenitor cells are present in articular cartilage from adult humans and that their frequency is increased in OA. This observation has implications for understanding the intrinsic repair capacity of articular cartilage and raises the possibility that these progenitor cells might be involved in the pathogenesis of arthritis.

摘要

跨膜受体Notch-1调节细胞命运和分化,有人提出它可识别新生牛关节软骨中具有祖细胞特征的细胞类型。我们发现,在早期传代的单层培养中,超过70%的骨髓间充质干细胞(BM-MSC)表达Notch-1。我们还证明,正常关节软骨含有Notch-1阳性细胞,且在骨关节炎(OA)中该频率增加。OA软骨中的大多数Notch-1阳性细胞位于增殖细胞簇中。这些发现表明,多能间充质祖细胞存在于成人关节软骨中,且在OA中其频率增加。这一观察结果对于理解关节软骨的内在修复能力具有重要意义,并增加了这些祖细胞可能参与关节炎发病机制的可能性。

相似文献

1
Mesenchymal progenitor cells in adult human articular cartilage.成年人类关节软骨中的间充质祖细胞。
Biorheology. 2006;43(3,4):447-54.
2
Age-related biological characterization of mesenchymal progenitor cells in human articular cartilage.人关节软骨中间充质祖细胞的年龄相关生物学特征
Orthopedics. 2011 Aug 8;34(8):e382-8. doi: 10.3928/01477447-20110627-06.
3
Progenitor Cells from Cartilage: Grade Specific Differences in Stem Cell Marker Expression.软骨来源的祖细胞:干细胞标志物表达的分级特异性差异
Int J Mol Sci. 2017 Aug 12;18(8):1759. doi: 10.3390/ijms18081759.
4
Identification of mesenchymal progenitor cells in normal and osteoarthritic human articular cartilage.正常和骨关节炎性人类关节软骨中间充质祖细胞的鉴定
Arthritis Rheum. 2004 May;50(5):1522-32. doi: 10.1002/art.20269.
5
Mesenchymal progenitor cell markers in human articular cartilage: normal distribution and changes in osteoarthritis.人关节软骨间充质祖细胞标志物:正常分布及在骨关节炎中的变化。
Arthritis Res Ther. 2009;11(3):R85. doi: 10.1186/ar2719. Epub 2009 Jun 5.
6
[Experimental study on CD105+/CD166+ cells and its chondrogenic potential in early osteoarthritis cartilage].[早期骨关节炎软骨中CD105+/CD166+细胞及其软骨形成潜能的实验研究]
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2013 Jul;27(7):793-9.
7
DCC is expressed in a CD166-positive subpopulation of chondrocytes in human osteoarthritic cartilage and modulates CRE activity.DCC在人类骨关节炎软骨中CD166阳性的软骨细胞亚群中表达,并调节CRE活性。
Int J Clin Exp Pathol. 2014 Apr 15;7(5):1947-56. eCollection 2014.
8
Relative percentage and zonal distribution of mesenchymal progenitor cells in human osteoarthritic and normal cartilage.人骨关节炎和正常软骨间充质祖细胞的相对百分比和分区分布。
Arthritis Res Ther. 2011 Apr 15;13(2):R64. doi: 10.1186/ar3320.
9
Characterization of human synovial fluid cells of 26 patients with osteoarthritis knee for cartilage repair therapy.对 26 例膝骨关节炎患者的滑液细胞进行特征分析,以用于软骨修复治疗。
Int J Rheum Dis. 2010 Feb 1;13(1):68-74. doi: 10.1111/j.1756-185X.2009.01456.x.
10
Restoration of the extracellular matrix in human osteoarthritic articular cartilage by overexpression of the transcription factor SOX9.通过转录因子SOX9的过表达恢复人骨关节炎关节软骨中的细胞外基质
Arthritis Rheum. 2007 Jan;56(1):158-67. doi: 10.1002/art.22299.

引用本文的文献

1
Glycosaminoglycans, Instructive Biomolecules That Regulate Cellular Activity and Synaptic Neuronal Control of Specific Tissue Functional Properties.糖胺聚糖,调节细胞活性和特定组织功能特性的突触神经元控制的指导性生物分子。
Int J Mol Sci. 2025 Mar 12;26(6):2554. doi: 10.3390/ijms26062554.
2
The application and progress of tissue engineering and biomaterial scaffolds for total auricular reconstruction in microtia.组织工程与生物材料支架在小耳畸形全耳再造中的应用与进展
Front Bioeng Biotechnol. 2023 Sep 22;11:1089031. doi: 10.3389/fbioe.2023.1089031. eCollection 2023.
3
From regeneration to osteoarthritis in the knee joint: The role shift of cartilage-derived progenitor cells.
从膝关节再生到骨关节炎:软骨来源祖细胞的角色转变
Front Cell Dev Biol. 2022 Oct 20;10:1010818. doi: 10.3389/fcell.2022.1010818. eCollection 2022.
4
Gene Expression and Chondrogenic Potential of Cartilage Cells: Osteoarthritis Grade Differences.软骨细胞的基因表达和软骨形成潜力:骨关节炎分级差异。
Int J Mol Sci. 2022 Sep 13;23(18):10610. doi: 10.3390/ijms231810610.
5
Endogenous repair theory enriches construction strategies for orthopaedic biomaterials: a narrative review.内源性修复理论丰富了骨科生物材料的构建策略:一项叙述性综述。
Biomater Transl. 2021 Dec 28;2(4):343-360. doi: 10.12336/biomatertransl.2021.04.008. eCollection 2021.
6
Increased migratory activity and cartilage regeneration by superficial-zone chondrocytes in enzymatically treated cartilage explants.酶处理软骨外植体中浅层区软骨细胞迁移活性和软骨再生增加。
BMC Musculoskelet Disord. 2022 Mar 16;23(1):256. doi: 10.1186/s12891-022-05210-2.
7
Meniscus Regeneration With Multipotent Stromal Cell Therapies.多能基质细胞疗法促进半月板再生
Front Bioeng Biotechnol. 2022 Feb 9;10:796408. doi: 10.3389/fbioe.2022.796408. eCollection 2022.
8
Novel cell sources for bone regeneration.用于骨再生的新型细胞来源。
MedComm (2020). 2021 May 4;2(2):145-174. doi: 10.1002/mco2.51. eCollection 2021 Jun.
9
Culture, Expansion and Differentiation of Mouse Bone-Derived Mesenchymal Stromal Cells.鼠源性骨髓间充质基质细胞的培养、扩增和分化。
Methods Mol Biol. 2021;2308:35-46. doi: 10.1007/978-1-0716-1425-9_3.
10
Comparison of the major cell populations among osteoarthritis, Kashin-Beck disease and healthy chondrocytes by single-cell RNA-seq analysis.单细胞 RNA 测序分析比较骨关节炎、大骨节病和健康软骨细胞中的主要细胞群体。
Cell Death Dis. 2021 May 27;12(6):551. doi: 10.1038/s41419-021-03832-3.