• 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

骨关节炎诱导的软骨钙化的分子机制研究。

The molecular mechanism research of cartilage calcification induced by osteoarthritis.

机构信息

Department of Sports Medicine, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.

Department of Orthopedics Surgery, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.

出版信息

Bioengineered. 2022 May;13(5):13082-13088. doi: 10.1080/21655979.2022.2078025.

DOI:10.1080/21655979.2022.2078025
PMID:35611765
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9276012/
Abstract

To explore the molecular mechanism of cartilage calcification induced by osteoarthritis (OA) based on distal-less homeobox gene 5 - alkaline phosphatase - integrin-binding sialoprotein - ecto-nucleotide pyrophosphatase 1 (DLX5-ALPL-IBSP-ENPP1) signal axis. Twenty-four rabbits were selected to build models of cartilage calcification induced by OA and randomly divided into 3 groups. The first group was the normal group whose rabbits were injected into 0.9% saline (0.3 mL), and the second group was model group. The third group was model group whose rabbits were injected into DLX5 antibody by caudal vein. Alizarin red calcium staining was used to analyze calcium deposition of cartilage matrix. Immunohistochemical staining was used to analyze the relative expression levels of proteins DLX5 and ENPP1, and western blot was used to analyze the DLX5, ALPL, IBSP, and ENPP1 expression. Calcium salt precipitation was the most serious, and the calcification area increased in the model group. Although calcified nodules appeared in the anti-DLX5 group, they were relatively few. Immunohistochemical staining analysis showed that the protein DLX5 located in the nucleus and the protein ENPP1 located in the extracellular matrix. Western blot analysis showed that the expressions of proteins DLX5, ALPL, IBSP, and ENPP1 were the highest in OA Model group than that of NC group, followed by anti-DLX5 group. The proteins DLX5, ALPL, IBSP, and ENPP1 can promote cartilage calcification induced by OA based on DLX5-ALPL-IBSP-ENPP1 signal axis.

摘要

探讨基于远侧板状同源框基因 5-碱性磷酸酶-整合素结合唾液蛋白-外核苷酸焦磷酸酶 1(DLX5-ALPL-IBSP-ENPP1)信号轴的骨关节炎(OA)诱导软骨钙化的分子机制。选择 24 只兔子建立 OA 诱导的软骨钙化模型,并随机分为 3 组。第 1 组为正常组,兔子注射 0.9%生理盐水(0.3 mL);第 2 组为模型组;第 3 组为模型组,尾静脉注射 DLX5 抗体。茜素红钙染色分析软骨基质钙沉积,免疫组化染色分析蛋白 DLX5 和 ENPP1 的相对表达水平,Western blot 分析 DLX5、ALPL、IBSP 和 ENPP1 的表达。模型组钙盐沉淀最严重,钙化面积增加。虽然抗-DLX5 组出现钙化结节,但相对较少。免疫组化染色分析显示,蛋白 DLX5 位于细胞核内,蛋白 ENPP1 位于细胞外基质中。Western blot 分析显示,OA 模型组中蛋白 DLX5、ALPL、IBSP 和 ENPP1 的表达均高于 NC 组,其次是抗-DLX5 组。蛋白 DLX5、ALPL、IBSP 和 ENPP1 可通过 DLX5-ALPL-IBSP-ENPP1 信号轴促进 OA 诱导的软骨钙化。

相似文献

1
The molecular mechanism research of cartilage calcification induced by osteoarthritis.骨关节炎诱导的软骨钙化的分子机制研究。
Bioengineered. 2022 May;13(5):13082-13088. doi: 10.1080/21655979.2022.2078025.
2
Inhibition of nucleotide pyrophosphatase/phosphodiesterase 1: implications for developing a calcium pyrophosphate deposition disease modifying drug.核苷酸焦磷酸酶/磷酸二酯酶 1 的抑制作用:开发焦磷酸钙沉积病修饰药物的意义。
Rheumatology (Oxford). 2018 Aug 1;57(8):1472-1480. doi: 10.1093/rheumatology/key092.
3
inhibits ectopic joint calcification and maintains articular chondrocytes by repressing hedgehog signaling.通过抑制 hedgehog 信号通路抑制异位关节钙化并维持关节软骨细胞。
Development. 2018 Sep 20;145(18):dev164830. doi: 10.1242/dev.164830.
4
Chondrocyte-derived exosomes promote cartilage calcification in temporomandibular joint osteoarthritis.软骨细胞来源的外泌体促进颞下颌关节骨关节炎的软骨钙化。
Arthritis Res Ther. 2022 Feb 14;24(1):44. doi: 10.1186/s13075-022-02738-5.
5
Anaphylatoxins and their corresponding receptors as potential drivers in cartilage calcification during osteoarthritis progression.过敏毒素及其相应受体作为骨关节炎进展过程中软骨钙化的潜在驱动因素。
Osteoarthritis Cartilage. 2024 May;32(5):514-525. doi: 10.1016/j.joca.2024.01.004. Epub 2024 Jan 17.
6
Adiponectin receptor agonist AdipoRon attenuates calcification of osteoarthritis chondrocytes by promoting autophagy.脂联素受体激动剂 AdipoRon 通过促进自噬来减轻骨关节炎软骨细胞的钙化。
J Cell Biochem. 2020 Jun;121(5-6):3333-3344. doi: 10.1002/jcb.29605. Epub 2020 Jan 3.
7
Abnormal Mechanical Loading Induces Cartilage Degeneration by Accelerating Meniscus Hypertrophy and Mineralization After ACL Injuries In Vivo.异常机械负荷通过加速前交叉韧带损伤后体内半月板肥大和矿化诱导软骨退变。
Am J Sports Med. 2016 Mar;44(3):652-63. doi: 10.1177/0363546515621285. Epub 2016 Jan 20.
8
Effects of GGCX overexpression on anterior cruciate ligament transection-induced osteoarthritis in rabbits.过表达 GGCX 对兔前交叉韧带切断诱导的骨关节炎的影响。
Mol Med Rep. 2018 Mar;17(3):3821-3828. doi: 10.3892/mmr.2017.8304. Epub 2017 Dec 18.
9
[The role and mechanism of S100 calcium binding protein B in osteoarthritis cartilage damage repair].[S100钙结合蛋白B在骨关节炎软骨损伤修复中的作用及机制]
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2018 Nov 15;32(11):1429-1434. doi: 10.7507/1002-1892.201804060.
10
Meniscal calcification, pathogenesis and implications.半月板钙化,发病机制与意义。
Curr Opin Rheumatol. 2012 Mar;24(2):152-7. doi: 10.1097/BOR.0b013e32834e90c1.

引用本文的文献

1
Two Members of Vitamin-K-Dependent Proteins, Gla-Rich Protein (GRP) and Matrix Gla Protein (MGP), as Possible New Players in the Molecular Mechanism of Osteoarthritis.维生素K依赖蛋白的两个成员,富含γ-羧基谷氨酸蛋白(GRP)和基质γ-羧基谷氨酸蛋白(MGP),可能是骨关节炎分子机制中的新参与者。
J Clin Med. 2024 Aug 30;13(17):5159. doi: 10.3390/jcm13175159.
2
Epitranscriptomic regulation of lipid oxidation and liver fibrosis via ENPP1 mRNA mA modification.通过 ENPP1 mRNA mA 修饰对脂质氧化和肝纤维化的转录后调控。
Cell Mol Life Sci. 2024 Sep 9;81(1):387. doi: 10.1007/s00018-024-05420-y.
3
Osteoarthritis: Insights into Diagnosis, Pathophysiology, Therapeutic Avenues, and the Potential of Natural Extracts.

本文引用的文献

1
DLX5 promotes osteosarcoma progression via activation of the NOTCH signaling pathway.DLX5通过激活NOTCH信号通路促进骨肉瘤进展。
Am J Cancer Res. 2021 Jun 15;11(6):3354-3374. eCollection 2021.
2
A biphasic visco-hyperelastic damage model for articular cartilage: application to micromechanical modelling of the osteoarthritis-induced degradation behaviour.一种用于关节软骨的双相黏弹损伤模型:在骨关节炎诱导的降解行为的细观力学建模中的应用。
Biomech Model Mechanobiol. 2020 Jun;19(3):1055-1077. doi: 10.1007/s10237-019-01270-x. Epub 2019 Dec 4.
3
Immunohistochemical and ultrastructural evaluation of matrix components in mandibular condylar cartilage in comparison with growth plate cartilage in cartilage calcification insufficient rats.
骨关节炎:关于诊断、病理生理学、治疗途径及天然提取物潜力的见解
Curr Issues Mol Biol. 2024 Apr 29;46(5):4063-4105. doi: 10.3390/cimb46050251.
4
A new perspective on intervertebral disc calcification-from bench to bedside.椎间盘钙化的新视角——从基础到临床。
Bone Res. 2024 Jan 22;12(1):3. doi: 10.1038/s41413-023-00307-3.
5
Integrated single-cell and bulk RNA sequencing analysis identified pyroptosis-related signature for diagnosis and prognosis in osteoarthritis.单细胞和 bulk RNA 测序分析的综合分析确定了骨关节炎诊断和预后的焦亡相关特征。
Sci Rep. 2023 Oct 18;13(1):17757. doi: 10.1038/s41598-023-44724-0.
6
Excessive sulfur oxidation in endoplasmic reticulum drives an inflammatory reaction of chondrocytes in aging mice.内质网中过度的硫氧化会引发衰老小鼠软骨细胞的炎症反应。
Front Pharmacol. 2022 Oct 24;13:1058469. doi: 10.3389/fphar.2022.1058469. eCollection 2022.
7
Genes in the Development and Maintenance of the Vertebrate Skeleton: Implications for Human Pathologies.脊椎动物骨骼发育和维持中的基因:对人类病理学的影响。
Cells. 2022 Oct 18;11(20):3277. doi: 10.3390/cells11203277.
8
Roles of the calcified cartilage layer and its tissue engineering reconstruction in osteoarthritis treatment.钙化软骨层在骨关节炎治疗中的作用及其组织工程重建
Front Bioeng Biotechnol. 2022 Aug 31;10:911281. doi: 10.3389/fbioe.2022.911281. eCollection 2022.
与软骨钙化不足大鼠生长板软骨相比,下颌髁突软骨基质成分的免疫组织化学和超微结构评估
Anat Sci Int. 2020 Jan;95(1):54-66. doi: 10.1007/s12565-019-00493-3. Epub 2019 Jun 14.
4
Down-regulation of miR-339 promotes differentiation of BMSCs and alleviates osteoporosis by targeting DLX5.miR-339的下调通过靶向DLX5促进骨髓间充质干细胞分化并减轻骨质疏松症。
Eur Rev Med Pharmacol Sci. 2019 Jan;23(1):29-36. doi: 10.26355/eurrev_201901_16744.
5
A NIR-II fluorescent probe for articular cartilage degeneration imaging and osteoarthritis detection.用于关节软骨退变成像和骨关节炎检测的近红外二区荧光探针。
Biomater Sci. 2019 Feb 26;7(3):1043-1051. doi: 10.1039/c8bm01440j.
6
Study of Endochondral Ossification in Human Fetalcartilage Anlagen of Metacarpals: Comparative Morphology of Mineral Deposition in Cartilage and in the Periosteal Bone Matrix.人胎儿掌骨软骨原基中软骨内成骨的研究:软骨及骨膜骨基质中矿物质沉积的比较形态学
Anat Rec (Hoboken). 2018 Apr;301(4):571-580. doi: 10.1002/ar.23756. Epub 2018 Jan 18.
7
What drives osteoarthritis?-synovial versus subchondral bone pathology.什么导致了骨关节炎?——滑膜与软骨下骨病理学。
Rheumatology (Oxford). 2017 Sep 1;56(9):1461-1471. doi: 10.1093/rheumatology/kew389.
8
Bone microdamage, remodeling and bone fragility: how much damage is too much damage?骨微损伤、重塑与骨脆性:多少损伤算过度损伤?
Bonekey Rep. 2015 Mar 18;4:644. doi: 10.1038/bonekey.2015.11. eCollection 2015.
9
Establishment of a novel dwarf rat strain: cartilage calcification insufficient (CCI) rats.一种新型侏儒大鼠品系的建立:软骨钙化不足(CCI)大鼠。
Exp Anim. 2015;64(2):121-8. doi: 10.1538/expanim.14-0072. Epub 2014 Dec 20.
10
Bone remodelling in osteoarthritis.骨关节炎中的骨重建。
Nat Rev Rheumatol. 2012 Nov;8(11):665-73. doi: 10.1038/nrrheum.2012.130. Epub 2012 Aug 7.