• 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

木糖基转移酶 I 介导具有长糖胺聚糖链的蛋白聚糖的合成,并控制生长板中的软骨细胞肥大和胶原纤维组织。

Xylosyltransferase I mediates the synthesis of proteoglycans with long glycosaminoglycan chains and controls chondrocyte hypertrophy and collagen fibers organization of in the growth plate.

机构信息

UMR 7365 CNRS-University of Lorraine, Biopôle, Faculty of Medicine, BP 20199, 54505, Vandoeuvre-lès-Nancy, CEDEX, France.

出版信息

Cell Death Dis. 2023 Jun 9;14(6):355. doi: 10.1038/s41419-023-05875-0.

DOI:10.1038/s41419-023-05875-0
PMID:37296099
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10256685/
Abstract

Genetic mutations in the Xylt1 gene are associated with Desbuquois dysplasia type II syndrome characterized by sever prenatal and postnatal short stature. However, the specific role of XylT-I in the growth plate is not completely understood. Here, we show that XylT-I is expressed and critical for the synthesis of proteoglycans in resting and proliferative but not in hypertrophic chondrocytes in the growth plate. We found that loss of XylT-I induces hypertrophic phenotype-like of chondrocytes associated with reduced interterritorial matrix. Mechanistically, deletion of XylT-I impairs the synthesis of long glycosaminoglycan chains leading to the formation of proteoglycans with shorter glycosaminoglycan chains. Histological and Second Harmonic Generation microscopy analysis revealed that deletion of XylT-I accelerated chondrocyte maturation and prevents chondrocytes columnar organization and arrangement in parallel of collagen fibers in the growth plate, suggesting that XylT-I controls chondrocyte maturation and matrix organization. Intriguingly, loss of XylT-I induced at embryonic stage E18.5 the migration of progenitor cells from the perichondrium next to the groove of Ranvier into the central part of epiphysis of E18.5 embryos. These cells characterized by higher expression of glycosaminoglycans exhibit circular organization then undergo hypertrophy and death creating a circular structure at the secondary ossification center location. Our study revealed an uncovered role of XylT-I in the synthesis of proteoglycans and provides evidence that the structure of glycosaminoglycan chains of proteoglycans controls chondrocyte maturation and matrix organization.

摘要

Xylt1 基因突变与 Desbuquois 发育不良 II 型综合征有关,该综合征的特征是严重的产前和产后身材矮小。然而,XylT-I 在生长板中的具体作用尚不完全清楚。在这里,我们表明 XylT-I 在生长板中的静止和增殖期软骨细胞中表达并对蛋白聚糖的合成至关重要,但在肥大期软骨细胞中则不然。我们发现,XylT-I 的缺失会诱导类似于肥大的软骨细胞表型,伴随着细胞外基质的减少。在机制上,XylT-I 的缺失会损害长糖胺聚糖链的合成,导致糖胺聚糖链较短的蛋白聚糖的形成。组织学和二次谐波产生显微镜分析显示,XylT-I 的缺失会加速软骨细胞成熟,并防止软骨细胞在生长板中沿胶原纤维平行排列成柱状组织和排列,表明 XylT-I 控制着软骨细胞的成熟和基质的组织。有趣的是,XylT-I 的缺失在胚胎期 E18.5 诱导了来自 Ranvier 沟旁的软骨膜祖细胞向 E18.5 胚胎骨骺中心的迁移。这些细胞表现出更高的糖胺聚糖表达,呈现出圆形组织,然后经历肥大和死亡,在二次骨化中心的位置形成一个圆形结构。我们的研究揭示了 XylT-I 在蛋白聚糖合成中的一个未被发现的作用,并提供了证据表明蛋白聚糖糖胺聚糖链的结构控制着软骨细胞的成熟和基质的组织。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8649/10256685/eaecbddd7439/41419_2023_5875_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8649/10256685/abf72b878ef7/41419_2023_5875_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8649/10256685/adbd1b518ed3/41419_2023_5875_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8649/10256685/376613e6aca0/41419_2023_5875_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8649/10256685/e9d198b41bd6/41419_2023_5875_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8649/10256685/e0ce79e0fc87/41419_2023_5875_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8649/10256685/a6c7f4cae81a/41419_2023_5875_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8649/10256685/eaecbddd7439/41419_2023_5875_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8649/10256685/abf72b878ef7/41419_2023_5875_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8649/10256685/adbd1b518ed3/41419_2023_5875_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8649/10256685/376613e6aca0/41419_2023_5875_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8649/10256685/e9d198b41bd6/41419_2023_5875_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8649/10256685/e0ce79e0fc87/41419_2023_5875_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8649/10256685/a6c7f4cae81a/41419_2023_5875_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8649/10256685/eaecbddd7439/41419_2023_5875_Fig7_HTML.jpg

相似文献

1
Xylosyltransferase I mediates the synthesis of proteoglycans with long glycosaminoglycan chains and controls chondrocyte hypertrophy and collagen fibers organization of in the growth plate.木糖基转移酶 I 介导具有长糖胺聚糖链的蛋白聚糖的合成,并控制生长板中的软骨细胞肥大和胶原纤维组织。
Cell Death Dis. 2023 Jun 9;14(6):355. doi: 10.1038/s41419-023-05875-0.
2
TMEM165 a new player in proteoglycan synthesis: loss of TMEM165 impairs elongation of chondroitin- and heparan-sulfate glycosaminoglycan chains of proteoglycans and triggers early chondrocyte differentiation and hypertrophy.TMEM165 是蛋白聚糖合成的新成员:TMEM165 的缺失会损害蛋白聚糖中软骨素和肝素硫酸糖胺聚糖链的延伸,并引发早期软骨细胞分化和肥大。
Cell Death Dis. 2021 Dec 20;13(1):11. doi: 10.1038/s41419-021-04458-1.
3
A dominant interference collagen X mutation disrupts hypertrophic chondrocyte pericellular matrix and glycosaminoglycan and proteoglycan distribution in transgenic mice.显性干扰性胶原蛋白X突变破坏转基因小鼠肥大软骨细胞的细胞周基质以及糖胺聚糖和蛋白聚糖的分布。
Am J Pathol. 2001 Dec;159(6):2257-69. doi: 10.1016/S0002-9440(10)63076-3.
4
Progression and recapitulation of the chondrocyte differentiation program: cartilage matrix protein is a marker for cartilage maturation.软骨细胞分化程序的进展与重现:软骨基质蛋白是软骨成熟的标志物。
Dev Biol. 1995 Nov;172(1):293-306. doi: 10.1006/dbio.1995.0024.
5
Microtubules are potential regulators of growth-plate chondrocyte differentiation and hypertrophy.微管是生长板软骨细胞分化和肥大的潜在调节因子。
Bone. 1999 Oct;25(4):405-12. doi: 10.1016/s8756-3282(99)00187-8.
6
Chondrocyte cell death and intracellular distribution of COMP and type IX collagen in the pseudoachondroplasia growth plate.假性软骨发育不全生长板中软骨细胞死亡及软骨寡聚基质蛋白(COMP)和IX型胶原的细胞内分布
J Orthop Res. 2004 Jul;22(4):759-67. doi: 10.1016/j.orthres.2003.11.010.
7
Developmental regulation of Wnt/beta-catenin signals is required for growth plate assembly, cartilage integrity, and endochondral ossification.Wnt/β-连环蛋白信号的发育调控对于生长板组装、软骨完整性和软骨内骨化是必需的。
J Biol Chem. 2005 May 13;280(19):19185-95. doi: 10.1074/jbc.M414275200. Epub 2005 Mar 10.
8
Cell Biological Assays for Measuring Chondrogenic Activities of CCN2 Protein.用于测量CCN2蛋白软骨生成活性的细胞生物学检测方法
Methods Mol Biol. 2017;1489:219-237. doi: 10.1007/978-1-4939-6430-7_21.
9
CANT1 deficiency in a mouse model of Desbuquois dysplasia impairs glycosaminoglycan synthesis and chondrocyte differentiation in growth plate cartilage.在 Desbuquois 发育不良的小鼠模型中 CANT1 缺乏会损害生长板软骨中的糖胺聚糖合成和软骨细胞分化。
FEBS Open Bio. 2020 Jun;10(6):1096-1103. doi: 10.1002/2211-5463.12859. Epub 2020 Apr 23.
10
Ascorbic acid-induced chondrocyte terminal differentiation: the role of the extracellular matrix and 1,25-dihydroxyvitamin D.抗坏血酸诱导的软骨细胞终末分化:细胞外基质和1,25-二羟维生素D的作用
Eur J Cell Biol. 1998 Jun;76(2):110-8. doi: 10.1016/s0171-9335(98)80023-x.

引用本文的文献

1
Deficiency of Human Mesenchymal Stem Cells: Impact on Osteogenic, Chondrogenic, and Adipogenic Differentiation.人骨髓间充质干细胞缺乏:对成骨、成软骨和成脂分化的影响。
Int J Mol Sci. 2025 Jul 30;26(15):7363. doi: 10.3390/ijms26157363.
2
CANT1 Is Involved in Collagen Fibrogenesis in Tendons by Regulating the Synthesis of Dermatan/Chondroitin Sulfate Attached to the Decorin Core Protein.CANT1通过调节附着于核心蛋白聚糖核心蛋白的硫酸皮肤素/硫酸软骨素的合成参与肌腱中的胶原纤维生成。
Int J Mol Sci. 2025 Mar 10;26(6):2463. doi: 10.3390/ijms26062463.
3
mRNA Degradation as a Therapeutic Solution for Mucopolysaccharidosis Type IIIC: Use of Antisense Oligonucleotides to Promote Downregulation of Heparan Sulfate Synthesis.

本文引用的文献

1
Regulation of Proliferation, Differentiation and Functions of Osteoblasts by Runx2.Runx2 对成骨细胞增殖、分化和功能的调节。
Int J Mol Sci. 2019 Apr 4;20(7):1694. doi: 10.3390/ijms20071694.
2
Periarticular Mesenchymal Progenitors Initiate and Contribute to Secondary Ossification Center Formation During Mouse Long Bone Development.关节周围间充质祖细胞在小鼠长骨发育过程中启动并有助于次生骨化中心的形成。
Stem Cells. 2019 May;37(5):677-689. doi: 10.1002/stem.2975. Epub 2019 Feb 6.
3
Possible Contribution of Wnt-Responsive Chondroprogenitors to the Postnatal Murine Growth Plate.
mRNA降解作为IIIC型黏多糖贮积症的一种治疗方案:使用反义寡核苷酸促进硫酸乙酰肝素合成的下调
Int J Mol Sci. 2025 Feb 1;26(3):1273. doi: 10.3390/ijms26031273.
4
Xylosyltransferase-Deficiency in Human Dermal Fibroblasts Induces Compensatory Myofibroblast Differentiation and Long-Term ECM Reduction.人皮肤成纤维细胞中的木糖基转移酶缺乏诱导代偿性肌成纤维细胞分化和长期细胞外基质减少。
Biomedicines. 2024 Mar 4;12(3):572. doi: 10.3390/biomedicines12030572.
5
Targeting FGFR3 signaling and drug repurposing for the treatment of SLC26A2-related chondrodysplasia in mouse model.靶向FGFR3信号通路及药物重新利用用于治疗小鼠模型中与SLC26A2相关的软骨发育不良
J Orthop Translat. 2024 Jan 6;44:88-101. doi: 10.1016/j.jot.2023.09.003. eCollection 2024 Jan.
Wnt反应性软骨祖细胞对出生后小鼠生长板的潜在贡献。
J Bone Miner Res. 2019 May;34(5):964-974. doi: 10.1002/jbmr.3658. Epub 2019 Jan 28.
4
In vitro and in vivo potentialities for cartilage repair from human advanced knee osteoarthritis synovial fluid-derived mesenchymal stem cells.人膝关节骨关节炎滑液来源间充质干细胞体外和体内修复软骨的潜能。
Stem Cell Res Ther. 2018 Nov 28;9(1):329. doi: 10.1186/s13287-018-1071-2.
5
Resting zone of the growth plate houses a unique class of skeletal stem cells.骺板静止区存在一类独特的骨骼干细胞。
Nature. 2018 Nov;563(7730):254-258. doi: 10.1038/s41586-018-0662-5. Epub 2018 Oct 31.
6
Quantitative Morphometry for Osteochondral Tissues Using Second Harmonic Generation Microscopy and Image Texture Information.基于二次谐波产生显微镜和图像纹理信息的软骨组织定量形态学研究
Sci Rep. 2018 Feb 12;8(1):2826. doi: 10.1038/s41598-018-21005-9.
7
Desbuquois dysplasia type II in a patient with a homozygous mutation in XYLT1 and new unusual findings.一名XYLT1基因纯合突变患者的II型德布凯发育不良及新的异常发现
Am J Med Genet A. 2016 Nov;170(11):3043-3047. doi: 10.1002/ajmg.a.37858. Epub 2016 Aug 2.
8
Tyrosine kinase inhibitor NVP-BGJ398 functionally improves FGFR3-related dwarfism in mouse model.酪氨酸激酶抑制剂NVP-BGJ398在小鼠模型中可有效改善与FGFR3相关的侏儒症。
J Clin Invest. 2016 May 2;126(5):1871-84. doi: 10.1172/JCI83926. Epub 2016 Apr 11.
9
The cartilage extracellular matrix as a transient developmental scaffold for growth plate maturation.软骨细胞外基质作为生长板成熟的短暂发育支架。
Matrix Biol. 2016 May-Jul;52-54:363-383. doi: 10.1016/j.matbio.2016.01.008. Epub 2016 Jan 23.
10
Structural and mechanical properties of the proliferative zone of the developing murine growth plate cartilage assessed by atomic force microscopy.通过原子力显微镜评估发育中小鼠生长板软骨增殖区的结构和力学性能。
Matrix Biol. 2016 Mar;50:1-15. doi: 10.1016/j.matbio.2015.10.001. Epub 2015 Oct 8.