• 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

硝苯地平对人骨髓或月经血来源间充质干细胞及软骨细胞成软骨分化的影响。

The Effect of CaV1.2 Inhibitor Nifedipine on Chondrogenic Differentiation of Human Bone Marrow or Menstrual Blood-Derived Mesenchymal Stem Cells and Chondrocytes.

机构信息

Department of Regenerative Medicine, State Research Institute Centre for Innovative Medicine, 08406 Vilnius, Lithuania.

Research Unit of Health Sciences and Technology, Faculty of Medicine, University of Oulu, 90014 Oulu, Finland.

出版信息

Int J Mol Sci. 2023 Apr 4;24(7):6730. doi: 10.3390/ijms24076730.

DOI:10.3390/ijms24076730
PMID:37047701
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10095444/
Abstract

Cartilage is an avascular tissue and sensitive to mechanical trauma and/or age-related degenerative processes leading to the development of osteoarthritis (OA). Therefore, it is important to investigate the mesenchymal cell-based chondrogenic regenerating mechanisms and possible their regulation. The aim of this study was to investigate the role of intracellular calcium (iCa) and its regulation through voltage-operated calcium channels (VOCC) on chondrogenic differentiation of mesenchymal stem/stromal cells derived from human bone marrow (BMMSCs) and menstrual blood (MenSCs) in comparison to OA chondrocytes. The level of iCa was highest in chondrocytes, whereas iCa store capacity was biggest in MenSCs and they proliferated better as compared to other cells. The level of CaV1.2 channels was also highest in OA chondrocytes than in other cells. CaV1.2 antagonist nifedipine slightly suppressed iCa, Cav1.2 and the proliferation of all cells and affected iCa stores, particularly in BMMSCs. The expression of the CaV1.2 gene during 21 days of chondrogenic differentiation was highest in MenSCs, showing the weakest chondrogenic differentiation, which was stimulated by the nifedipine. The best chondrogenic differentiation potential showed BMMSCs ( and expression); however, purposeful iCa and VOCC regulation by blockers can stimulate a chondrogenic response at least in MenSCs.

摘要

软骨是一种无血管组织,对机械性创伤和/或与年龄相关的退行性过程敏感,导致骨关节炎(OA)的发生。因此,研究基于间充质细胞的软骨再生机制及其可能的调节作用非常重要。本研究旨在研究细胞内钙(iCa)及其通过电压门控钙通道(VOCC)的调节在骨髓间充质干细胞(BMMSCs)和月经血间充质干细胞(MenSCs)向软骨细胞分化中的作用,并与 OA 软骨细胞进行比较。iCa 水平在软骨细胞中最高,而 iCa 储存能力在 MenSCs 中最大,它们的增殖能力比其他细胞更好。CaV1.2 通道的水平在 OA 软骨细胞中也高于其他细胞。CaV1.2 拮抗剂硝苯地平轻微抑制 iCa、Cav1.2 和所有细胞的增殖,并影响 iCa 储存,特别是在 BMMSCs 中。在 21 天的软骨分化过程中,CaV1.2 基因的表达在 MenSCs 中最高,但其软骨分化能力最弱,这一过程被硝苯地平刺激。BMMSCs 表现出最强的软骨分化潜力(和 表达);然而,通过阻断剂有目的地调节 iCa 和 VOCC 可以至少在 MenSCs 中刺激软骨反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4a/10095444/5968fb7357eb/ijms-24-06730-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4a/10095444/c06459ba4597/ijms-24-06730-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4a/10095444/83d3f5fe6ff1/ijms-24-06730-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4a/10095444/784070716686/ijms-24-06730-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4a/10095444/884021c53aac/ijms-24-06730-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4a/10095444/d26b630a10ca/ijms-24-06730-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4a/10095444/58fd39072669/ijms-24-06730-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4a/10095444/5968fb7357eb/ijms-24-06730-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4a/10095444/c06459ba4597/ijms-24-06730-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4a/10095444/83d3f5fe6ff1/ijms-24-06730-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4a/10095444/784070716686/ijms-24-06730-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4a/10095444/884021c53aac/ijms-24-06730-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4a/10095444/d26b630a10ca/ijms-24-06730-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4a/10095444/58fd39072669/ijms-24-06730-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4a/10095444/5968fb7357eb/ijms-24-06730-g007.jpg

相似文献

1
The Effect of CaV1.2 Inhibitor Nifedipine on Chondrogenic Differentiation of Human Bone Marrow or Menstrual Blood-Derived Mesenchymal Stem Cells and Chondrocytes.硝苯地平对人骨髓或月经血来源间充质干细胞及软骨细胞成软骨分化的影响。
Int J Mol Sci. 2023 Apr 4;24(7):6730. doi: 10.3390/ijms24076730.
2
Different phenotypes and chondrogenic responses of human menstrual blood and bone marrow mesenchymal stem cells to activin A and TGF-β3.人月经血和骨髓间充质干细胞对激活素 A 和 TGF-β3 的不同表型和软骨生成反应。
Stem Cell Res Ther. 2021 Apr 29;12(1):251. doi: 10.1186/s13287-021-02286-w.
3
The Effects of Mechanical Load on Chondrogenic Responses of Bone Marrow Mesenchymal Stem Cells and Chondrocytes Encapsulated in Chondroitin Sulfate-Based Hydrogel.机械载荷对包埋于硫酸软骨素水凝胶中的骨髓间充质干细胞和软骨细胞的软骨生成反应的影响。
Int J Mol Sci. 2023 Feb 2;24(3):2915. doi: 10.3390/ijms24032915.
4
Oral Administration of Strontium Gluconate Effectively Reduces Articular Cartilage Degeneration Through Enhanced Anabolic Activity of Chondrocytes and Chondrogenetic Differentiation of Mesenchymal Stromal Cells.口服葡萄糖酸锶通过增强软骨细胞的合成代谢活性和间充质基质细胞的软骨分化作用,有效减轻关节软骨退变。
Biol Trace Elem Res. 2020 Feb;193(2):422-433. doi: 10.1007/s12011-019-01711-9. Epub 2019 May 3.
5
Characterization and use of Equine Bone Marrow Mesenchymal Stem Cells in Equine Cartilage Engineering. Study of their Hyaline Cartilage Forming Potential when Cultured under Hypoxia within a Biomaterial in the Presence of BMP-2 and TGF-ß1.马骨髓间充质干细胞的特性及其在马软骨工程中的应用。研究在 BMP-2 和 TGF-ß1 存在的情况下,在生物材料中于低氧条件下培养时其形成透明软骨的潜力。
Stem Cell Rev Rep. 2017 Oct;13(5):611-630. doi: 10.1007/s12015-017-9748-y.
6
Menstrual Blood-Derived Stem Cell Paracrine Factors Possess Stimulatory Effects on Chondrogenesis In Vitro and Diminish the Degradation of Articular Cartilage during Osteoarthritis.月经血源性干细胞旁分泌因子对体外软骨生成具有刺激作用,并可减轻骨关节炎期间关节软骨的降解。
Bioengineering (Basel). 2023 Aug 24;10(9):1001. doi: 10.3390/bioengineering10091001.
7
The Antihypertensive Drug Nifedipine Modulates the Metabolism of Chondrocytes and Human Bone Marrow-Derived Mesenchymal Stem Cells.抗高血压药物硝苯地平调节软骨细胞和人骨髓间充质干细胞的代谢。
Front Endocrinol (Lausanne). 2019 Nov 8;10:756. doi: 10.3389/fendo.2019.00756. eCollection 2019.
8
Chondrogenic induction of human osteoarthritic cartilage-derived mesenchymal stem cells activates mineralization and hypertrophic and osteogenic gene expression through a mechanomiR.人骨性关节炎软骨来源间充质干细胞的软骨诱导通过机械 microRNA 激活矿化及肥大和成骨基因表达。
Arthritis Res Ther. 2019 Jul 8;21(1):167. doi: 10.1186/s13075-019-1949-0.
9
Chondrogenic differentiation of bovine bone marrow mesenchymal stem cells (MSCs) in different hydrogels: influence of collagen type II extracellular matrix on MSC chondrogenesis.牛骨髓间充质干细胞(MSCs)在不同水凝胶中的软骨分化:II型胶原细胞外基质对MSCs软骨形成的影响
Biotechnol Bioeng. 2006 Apr 20;93(6):1152-63. doi: 10.1002/bit.20828.
10
Comparison of the Chondrogenic Potential of Mesenchymal Stem Cells Derived from Bone Marrow and Umbilical Cord Blood Intended for Cartilage Tissue Engineering.比较骨髓和脐带来源的间充质干细胞在软骨组织工程中的成软骨潜力。
Stem Cell Rev Rep. 2020 Feb;16(1):126-143. doi: 10.1007/s12015-019-09914-2.

引用本文的文献

1
The Effect of TGF-β3 and IL-1β on L-Type Voltage-Operated Calcium Channels and Calcium Ion Homeostasis in Osteoarthritic Chondrocytes and Human Bone Marrow-Derived Mesenchymal Stem Cells During Chondrogenesis.转化生长因子-β3(TGF-β3)和白细胞介素-1β(IL-1β)对骨关节炎软骨细胞和人骨髓间充质干细胞软骨形成过程中L型电压门控钙通道及钙离子稳态的影响
Pharmaceutics. 2025 Mar 7;17(3):343. doi: 10.3390/pharmaceutics17030343.
2
The study on bone marrow mesenchymal stem cell-derived extracellular matrix promoting the repair of damaged chondrocytes by regulating the Notch1/RBPJ pathway.骨髓间充质干细胞衍生的细胞外基质通过调节Notch1/RBPJ通路促进受损软骨细胞修复的研究
Cytotechnology. 2025 Feb;77(1):35. doi: 10.1007/s10616-024-00702-6. Epub 2025 Jan 4.
3

本文引用的文献

1
Chondroitin Sulfate-Tyramine-Based Hydrogels for Cartilage Tissue Repair.用于软骨组织修复的硫酸软骨素-酪胺基水凝胶
Int J Mol Sci. 2023 Feb 9;24(4):3451. doi: 10.3390/ijms24043451.
2
The Effects of Mechanical Load on Chondrogenic Responses of Bone Marrow Mesenchymal Stem Cells and Chondrocytes Encapsulated in Chondroitin Sulfate-Based Hydrogel.机械载荷对包埋于硫酸软骨素水凝胶中的骨髓间充质干细胞和软骨细胞的软骨生成反应的影响。
Int J Mol Sci. 2023 Feb 2;24(3):2915. doi: 10.3390/ijms24032915.
3
The Emerging Role of Menstrual-Blood-Derived Stem Cells in Endometriosis.
Regulation of pain neurotransmitters and chondrocytes metabolism mediated by voltage-gated ion channels: A narrative review.电压门控离子通道介导的疼痛神经递质调节与软骨细胞代谢:一篇叙述性综述。
Heliyon. 2023 Jul 5;9(7):e17989. doi: 10.1016/j.heliyon.2023.e17989. eCollection 2023 Jul.
经血来源干细胞在子宫内膜异位症中的新作用
Biomedicines. 2022 Dec 24;11(1):39. doi: 10.3390/biomedicines11010039.
4
Differences in the intrinsic chondrogenic potential of human mesenchymal stromal cells and iPSC-derived multipotent cells.人骨髓间充质基质细胞与 iPSC 来源的多能细胞内在的软骨生成潜能的差异。
Clin Transl Med. 2022 Dec;12(12):e1112. doi: 10.1002/ctm2.1112.
5
Integrins, cadherins and channels in cartilage mechanotransduction: perspectives for future regeneration strategies.软骨机械转导中的整合素、钙黏蛋白和通道:未来再生策略的展望。
Expert Rev Mol Med. 2021 Oct 27;23:e14. doi: 10.1017/erm.2021.16.
6
Cardiovascular Drugs and Osteoarthritis: Effects of Targeting Ion Channels.心血管药物与骨关节炎:靶向离子通道的作用。
Cells. 2021 Sep 28;10(10):2572. doi: 10.3390/cells10102572.
7
Different phenotypes and chondrogenic responses of human menstrual blood and bone marrow mesenchymal stem cells to activin A and TGF-β3.人月经血和骨髓间充质干细胞对激活素 A 和 TGF-β3 的不同表型和软骨生成反应。
Stem Cell Res Ther. 2021 Apr 29;12(1):251. doi: 10.1186/s13287-021-02286-w.
8
Various Aspects of Calcium Signaling in the Regulation of Apoptosis, Autophagy, Cell Proliferation, and Cancer.钙信号在细胞凋亡、自噬、细胞增殖和癌症调控中的各种作用。
Int J Mol Sci. 2020 Nov 6;21(21):8323. doi: 10.3390/ijms21218323.
9
Expansion and Chondrogenic Differentiation of Human Bone Marrow-Derived Mesenchymal Stromal Cells.人骨髓间充质基质细胞的扩增和软骨分化。
Methods Mol Biol. 2021;2221:15-28. doi: 10.1007/978-1-0716-0989-7_2.
10
Physiopathology of the Permeability Transition Pore: Molecular Mechanisms in Human Pathology.通透性转换孔的病理生理学:人类病理学中的分子机制。
Biomolecules. 2020 Jul 4;10(7):998. doi: 10.3390/biom10070998.