• 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

胰岛素样生长因子1诱导的人脐带华通氏胶间充质干细胞条件培养基(IGF1-hWJMSCs-CM)对骨关节炎的影响

Effect of Conditioned Medium from IGF1-Induced Human Wharton's Jelly Mesenchymal Stem Cells (IGF1-hWJMSCs-CM) on Osteoarthritis.

作者信息

Kusuma Hanna Sari Widya, Widowati Wahyu, Gunanegara Rimonta Febby, Juliandi Berry, Lister Nyoman Ehrich, Arumwardana Seila, Yusepany Dewani Tediana, Artie Dwi Surya, Nataya Enden Dea, Gunawan Kamila Yashfa, Sholihah Ika Adhani, Girsang Ermi, Ginting Chrismis Novalinda, Bachtiar Indra, Murti Harry

机构信息

Biomolecular and Biomedical Research Center, Aretha Medika, Utama, Bandung, West Java, Indonesia.

Faculty of Medicine, Maranatha Christian University, Bandung, West Java, Indonesia.

出版信息

Avicenna J Med Biotechnol. 2020 Jul-Sep;12(3):172-178.

PMID:32695280
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7368112/
Abstract

BACKGROUND

Osteoarthritis (OA) is a chronic disease that attacks joints and bones which can be caused by trauma or other joint diseases. Stem cell and Conditioned Medium (CM) of stem cells are developed for OA therapy, which is minimally invasive. It can decrease inflammation and be a replacement for knee surgery. This study aimed to utilize human Wharton's Jelly-Mesenchymal Stem Cells (hWJMSCs) as an alternative OA therapy.

METHODS

CM from hWJMSCs induced by IGF1 was collected. The OA cells model (IL1β-CHON002) culture was treated as follows: 1) with hWJMSCs-CM 15% (v/v); 2) with hWJMSCs-CM 30% (v/v); 3) with IGF1-hWJMSCs (IGF1-hWJMSCs-CM) 15% (v/v); 4) with IGF1-hWJMSCs-CM 30% (v/v). Parameters including inflammatory cytokines (IL10 and TNFα), extracellular matrix degradation (MMP3 expression), and chondrogenic marker ( expression) were determined.

RESULTS

The most significant increase in chondrogenic markers was found in IL1β-CHON002 treatment using 15% CM of hWJMSCs induced with IGF1. CM of hWJMSCs can reduce inflammatory cytokines (TNFα and IL10) and matrix degradation mediator MMP3. Better result was gained from IGF1-induced hWJMSCs-CM.

CONCLUSION

CM of IGF1-hWJMSCs reduce inflammation while repairing injured joint in the human chondrocyte OA model.

摘要

背景

骨关节炎(OA)是一种侵袭关节和骨骼的慢性疾病,可由创伤或其他关节疾病引起。干细胞和干细胞条件培养基(CM)被开发用于OA治疗,这种治疗微创,可减轻炎症,有望替代膝关节手术。本研究旨在利用人脐带华通氏胶间充质干细胞(hWJMSCs)作为OA的替代治疗方法。

方法

收集由IGF1诱导的hWJMSCs的CM。OA细胞模型(IL1β-CHON002)培养物按以下方式处理:1)用15%(v/v)的hWJMSCs-CM;2)用30%(v/v)的hWJMSCs-CM;3)用15%(v/v)的IGF1-hWJMSCs(IGF1-hWJMSCs-CM);4)用30%(v/v)的IGF1-hWJMSCs-CM。测定包括炎性细胞因子(IL10和TNFα)、细胞外基质降解(MMP3表达)和成软骨标志物(表达)等参数。

结果

在用IGF1诱导的hWJMSCs的15% CM处理IL1β-CHON002时,成软骨标志物的增加最为显著。hWJMSCs的CM可降低炎性细胞因子(TNFα和IL10)和基质降解介质MMP3。IGF1诱导的hWJMSCs-CM取得了更好的效果。

结论

IGF1-hWJMSCs的CM在修复人类软骨细胞OA模型中受损关节的同时减轻炎症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e53/7368112/17c8c28fdf85/AJMB-12-172-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e53/7368112/23ca3bbcd3c8/AJMB-12-172-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e53/7368112/182fe33bbd3b/AJMB-12-172-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e53/7368112/304248f3a7c9/AJMB-12-172-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e53/7368112/17c8c28fdf85/AJMB-12-172-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e53/7368112/23ca3bbcd3c8/AJMB-12-172-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e53/7368112/182fe33bbd3b/AJMB-12-172-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e53/7368112/304248f3a7c9/AJMB-12-172-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e53/7368112/17c8c28fdf85/AJMB-12-172-g004.jpg

相似文献

1
Effect of Conditioned Medium from IGF1-Induced Human Wharton's Jelly Mesenchymal Stem Cells (IGF1-hWJMSCs-CM) on Osteoarthritis.胰岛素样生长因子1诱导的人脐带华通氏胶间充质干细胞条件培养基(IGF1-hWJMSCs-CM)对骨关节炎的影响
Avicenna J Med Biotechnol. 2020 Jul-Sep;12(3):172-178.
2
Conditioned medium of IGF1-induced synovial membrane mesenchymal stem cells increases chondrogenic and chondroprotective markers in chondrocyte inflammation.IGF1 诱导的滑膜间充质干细胞条件培养基增加软骨细胞炎症中的软骨生成和软骨保护标志物。
Biosci Rep. 2021 Jul 30;41(7). doi: 10.1042/BSR20202038.
3
Effects of insulin-like growth factor-induced Wharton jelly mesenchymal stem cells toward chondrogenesis in an osteoarthritis model.胰岛素样生长因子诱导的华通氏胶间充质干细胞对骨关节炎模型软骨形成的影响。
Iran J Basic Med Sci. 2018 Jul;21(7):745-752. doi: 10.22038/IJBMS.2018.28205.6840.
4
In vitro differentiation process of human Wharton's jelly mesenchymal stem cells to male germ cells in the presence of gonadal and non-gonadal conditioned media with retinoic acid.在存在性腺和非性腺条件培养基及视黄酸的情况下,人脐带华通氏胶间充质干细胞向雄性生殖细胞的体外分化过程。
In Vitro Cell Dev Biol Anim. 2015 Nov;51(10):1093-101. doi: 10.1007/s11626-015-9929-4. Epub 2015 Oct 1.
5
Comparison of the Expression of Hepatic Genes by Human Wharton's Jelly Mesenchymal Stem Cells Cultured in 2D and 3D Collagen Culture Systems.二维和三维胶原蛋白培养系统中培养的人脐带华通氏胶间充质干细胞肝脏基因表达的比较
Iran J Med Sci. 2016 Jan;41(1):28-36.
6
Human umbilical cord Wharton's jelly mesenchymal stem cells combined with an acellular cartilage extracellular matrix scaffold improve cartilage repair compared with microfracture in a caprine model.人脐带华通氏胶间充质干细胞联合去细胞软骨细胞外基质支架修复软骨优于微骨折在山羊模型。
Osteoarthritis Cartilage. 2018 Jul;26(7):954-965. doi: 10.1016/j.joca.2018.01.019. Epub 2018 Jan 31.
7
Immune characterization of mesenchymal stem cells in human umbilical cord Wharton's jelly and derived cartilage cells.人脐带华通氏胶间充质干细胞及其衍生软骨细胞的免疫特性研究。
Cell Immunol. 2012 Jul-Aug;278(1-2):35-44. doi: 10.1016/j.cellimm.2012.06.010. Epub 2012 Jul 16.
8
MSCs can be differentially isolated from maternal, middle and fetal segments of the human umbilical cord.间充质干细胞可以从人脐带的母体段、中间段和胎儿段中进行差异性分离。
Cytotherapy. 2016 Dec;18(12):1493-1502. doi: 10.1016/j.jcyt.2016.08.003. Epub 2016 Oct 7.
9
Hepatogenic Differentiation Capacity of Human Wharton's Jelly Mesenchymal Stem Cell in a Co-culturing System with Endothelial Cells in Matrigel/collagen Scaffold in the Presence of Fetal Liver Extract.在含有胎肝提取物的基质胶/胶原蛋白支架中,人脐带华通氏胶间充质干细胞与内皮细胞共培养体系中的肝源性分化能力。
Int J Stem Cells. 2017 Nov 30;10(2):218-226. doi: 10.15283/ijsc17003.
10
Conditioned Medium of Wharton's Jelly Derived Stem Cells Can Enhance the Cartilage Specific Genes Expression by Chondrocytes in Monolayer and Mass Culture Systems.脐带来源干细胞的条件培养基可增强单层和团块培养系统中软骨细胞的软骨特异性基因表达。
Adv Pharm Bull. 2017 Apr;7(1):123-130. doi: 10.15171/apb.2017.016. Epub 2017 Apr 13.

引用本文的文献

1
Wharton's jelly and osteoarthritis of the knee.牙髓基质和膝关节骨关节炎。
Br Med Bull. 2024 Mar 13;149(1):13-31. doi: 10.1093/bmb/ldad030.
2
Conditioned Medium - Is it an Undervalued Lab Waste with the Potential for Osteoarthritis Management?条件培养基——它是一种被低估的实验室废物,具有治疗骨关节炎的潜力吗?
Stem Cell Rev Rep. 2023 Jul;19(5):1185-1213. doi: 10.1007/s12015-023-10517-1. Epub 2023 Feb 15.
3
Comprehensive analysis of potential ceRNA network and immune cell infiltration in intervertebral disc degeneration.椎间盘退变中 ceRNA 网络和免疫细胞浸润的综合分析

本文引用的文献

1
Effects of insulin-like growth factor-induced Wharton jelly mesenchymal stem cells toward chondrogenesis in an osteoarthritis model.胰岛素样生长因子诱导的华通氏胶间充质干细胞对骨关节炎模型软骨形成的影响。
Iran J Basic Med Sci. 2018 Jul;21(7):745-752. doi: 10.22038/IJBMS.2018.28205.6840.
2
Biomarkers of early stage osteoarthritis, rheumatoid arthritis and musculoskeletal health.早期骨关节炎、类风湿关节炎和肌肉骨骼健康的生物标志物。
Sci Rep. 2015 Mar 19;5:9259. doi: 10.1038/srep09259.
3
Green tea polyphenol treatment is chondroprotective, anti-inflammatory and palliative in a mouse post-traumatic osteoarthritis model.
J Orthop Surg Res. 2022 Sep 29;17(1):432. doi: 10.1186/s13018-022-03331-x.
4
Attenuation of osteoarthritis progression through intra-articular injection of a combination of synovial membrane-derived MSCs (SMMSCs), platelet-rich plasma (PRP) and conditioned medium (secretome).通过关节内注射滑膜来源的间充质干细胞(SMMSCs)、富血小板血浆(PRP)和条件培养基(分泌组)的混合物来抑制骨关节炎的进展。
J Orthop Surg Res. 2022 Feb 17;17(1):102. doi: 10.1186/s13018-021-02851-2.
5
Decreased Inhibition of Proliferation and Induction of Apoptosis in Breast Cancer Cell Lines (T47D and MCF7) from Treatment with Conditioned Medium Derived from Hypoxia-Treated Wharton's Jelly MSCs Compared with Normoxia-Treated MSCs.与常氧处理的沃顿胶间充质干细胞相比,低氧处理的沃顿胶间充质干细胞条件培养基处理乳腺癌细胞系(T47D和MCF7)后,对细胞增殖的抑制作用减弱,诱导凋亡的作用降低。
Int J Hematol Oncol Stem Cell Res. 2021 Apr 1;15(2):77-89. doi: 10.18502/ijhoscr.v15i2.6038.
6
Conditioned medium of IGF1-induced synovial membrane mesenchymal stem cells increases chondrogenic and chondroprotective markers in chondrocyte inflammation.IGF1 诱导的滑膜间充质干细胞条件培养基增加软骨细胞炎症中的软骨生成和软骨保护标志物。
Biosci Rep. 2021 Jul 30;41(7). doi: 10.1042/BSR20202038.
在小鼠创伤后骨关节炎模型中,绿茶多酚治疗具有软骨保护、抗炎和缓解作用。
Arthritis Res Ther. 2014 Dec 17;16(6):508. doi: 10.1186/s13075-014-0508-y.
4
The role of inflammatory and anti-inflammatory cytokines in the pathogenesis of osteoarthritis.炎症和抗炎细胞因子在骨关节炎发病机制中的作用。
Mediators Inflamm. 2014;2014:561459. doi: 10.1155/2014/561459. Epub 2014 Apr 30.
5
Protein synthesis and secretion in human mesenchymal cells derived from bone marrow, adipose tissue and Wharton's jelly.源自骨髓、脂肪组织和脐带华通氏胶的人间充质细胞中的蛋白质合成与分泌
Stem Cell Res Ther. 2014 Apr 16;5(2):53. doi: 10.1186/scrt442.
6
Mesenchymal stem cells for cartilage repair in osteoarthritis.用于骨关节炎软骨修复的间充质干细胞
Stem Cell Res Ther. 2012 Jul 9;3(4):25. doi: 10.1186/scrt116.
7
Direct transplantation of mesenchymal stem cells into the knee joints of Hartley strain guinea pigs with spontaneous osteoarthritis.将间充质干细胞直接移植到自发性骨关节炎哈特里株豚鼠膝关节中。
Arthritis Res Ther. 2012 Feb 7;14(1):R31. doi: 10.1186/ar3735.
8
Plasma proteins present in osteoarthritic synovial fluid can stimulate cytokine production via Toll-like receptor 4.骨关节炎滑液中存在的血浆蛋白可通过 Toll 样受体 4 刺激细胞因子产生。
Arthritis Res Ther. 2012 Jan 8;14(1):R7. doi: 10.1186/ar3555.
9
Time-dependent processes in stem cell-based tissue engineering of articular cartilage.基于干细胞的关节软骨组织工程中的时变过程。
Stem Cell Rev Rep. 2012 Sep;8(3):863-81. doi: 10.1007/s12015-011-9328-5.
10
Mesenchymal stem cell-based tissue engineering for chondrogenesis.基于间充质干细胞的软骨形成组织工程
J Biomed Biotechnol. 2011;2011:806891. doi: 10.1155/2011/806891. Epub 2011 Oct 9.