Stem cell-mediated bone regeneration of marine-derived fibrinolytic compound (FGFC-1) loaded carboxymethyl chitosan hydrogels

IF 6.9 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Lakshmi Jeevithan , Wang Shuyue , Sabu Thomas , Jose Eduardo Mate Sanchez de Val , Wenhui Wu , Jeevithan Elango
{"title":"Stem cell-mediated bone regeneration of marine-derived fibrinolytic compound (FGFC-1) loaded carboxymethyl chitosan hydrogels","authors":"Lakshmi Jeevithan ,&nbsp;Wang Shuyue ,&nbsp;Sabu Thomas ,&nbsp;Jose Eduardo Mate Sanchez de Val ,&nbsp;Wenhui Wu ,&nbsp;Jeevithan Elango","doi":"10.1016/j.biopha.2025.118162","DOIUrl":null,"url":null,"abstract":"<div><div>Carboxymethyl chitosan (CMC)-based hydrogels (HG) have gained significant attention for therapeutic applications due to their biomimetic properties and biocompatibility. This study explores, for the first time, the regenerative and osteogenic potential of CMC-HG incorporated with a marine fungi-derived fibrinolytic compound, FGFC-1. The inclusion of FGFC-1 did not significantly alter the crucial characteristics of the HGs, including secondary structure, thermal stability, protein adhesion, and in vitro degradation. However, incorporation of FGFC1 increased the swelling capacity (from 132.88 % to 157.11 %) and decreased the mineral adhesion (0.416 at 0.1 mg/ml) and porosity (from 72.95 % to 54.29 %). In general, the bacterial adhesion was decreased by 44.3 % in HG than control., Optimal culture conditions for mesenchymal stem cells (MSCs) were achieved with 2 % CMC and FGFC-1 concentrations of 0.01–1 mg/ml (<span><span>Supplementary Fig. S2</span></span><strong>)</strong>, supporting significant MSC growth. SEM image proved more interconnected dense fibrillar clustered morphology of MSCs on HGs than 2D. FGFC-1 accelerated osteogenic differentiation of MSCs by increasing mRNA expression levels of Runx2 (4.98), collagen-1 alpha-1 (3.4), osteocalcin (3.62), and ALP (4.20), which was further validated through enhanced staining for alizarin red, von Kossa, and alkaline phosphatase, as well as immunostaining for osteocollagen and osteocalcin in differentiated MSCs within the hydrogels. Notably, FGFC-1 significantly induced osteogenic differentiation along with supplements. These findings highlight FGFC-1-loaded CMC hydrogels as a promising strategy for stem cell-mediated bone regeneration in biomedical applications.</div></div>","PeriodicalId":8966,"journal":{"name":"Biomedicine & Pharmacotherapy","volume":"188 ","pages":"Article 118162"},"PeriodicalIF":6.9000,"publicationDate":"2025-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomedicine & Pharmacotherapy","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0753332225003567","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0

Abstract

Carboxymethyl chitosan (CMC)-based hydrogels (HG) have gained significant attention for therapeutic applications due to their biomimetic properties and biocompatibility. This study explores, for the first time, the regenerative and osteogenic potential of CMC-HG incorporated with a marine fungi-derived fibrinolytic compound, FGFC-1. The inclusion of FGFC-1 did not significantly alter the crucial characteristics of the HGs, including secondary structure, thermal stability, protein adhesion, and in vitro degradation. However, incorporation of FGFC1 increased the swelling capacity (from 132.88 % to 157.11 %) and decreased the mineral adhesion (0.416 at 0.1 mg/ml) and porosity (from 72.95 % to 54.29 %). In general, the bacterial adhesion was decreased by 44.3 % in HG than control., Optimal culture conditions for mesenchymal stem cells (MSCs) were achieved with 2 % CMC and FGFC-1 concentrations of 0.01–1 mg/ml (Supplementary Fig. S2), supporting significant MSC growth. SEM image proved more interconnected dense fibrillar clustered morphology of MSCs on HGs than 2D. FGFC-1 accelerated osteogenic differentiation of MSCs by increasing mRNA expression levels of Runx2 (4.98), collagen-1 alpha-1 (3.4), osteocalcin (3.62), and ALP (4.20), which was further validated through enhanced staining for alizarin red, von Kossa, and alkaline phosphatase, as well as immunostaining for osteocollagen and osteocalcin in differentiated MSCs within the hydrogels. Notably, FGFC-1 significantly induced osteogenic differentiation along with supplements. These findings highlight FGFC-1-loaded CMC hydrogels as a promising strategy for stem cell-mediated bone regeneration in biomedical applications.
载羧甲基壳聚糖水凝胶的海洋纤维蛋白溶解化合物(FGFC-1)干细胞介导的骨再生
羧甲基壳聚糖(CMC)基水凝胶(HG)因其具有仿生性能和生物相容性而受到广泛关注。本研究首次探索了CMC-HG与海洋真菌来源的纤维蛋白溶解化合物FGFC-1结合的再生和成骨潜力。FGFC-1的加入并没有显著改变HGs的关键特性,包括二级结构、热稳定性、蛋白质粘附性和体外降解。然而,FGFC1的掺入增加了溶胀能力(从132.88 %增加到157.11 %),降低了矿物粘附性(0.1 mg/ml时为0.416)和孔隙率(从72.95 %减少到54.29 %)。总体而言,HG组细菌粘附比对照组降低44.3% %。间充质干细胞(MSCs)的最佳培养条件为2 % CMC和0.01 - mg/ml的FGFC-1浓度(补充图S2),支持MSC的显著生长。扫描电镜图像显示,HGs上的间充质干细胞比二维图像更具有相互连接的致密纤维簇状形态。FGFC-1通过提高Runx2(4.98)、collagen-1 α -1(3.4)、osteocalcin(3.62)、ALP (4.20) mRNA的表达水平加速MSCs的成骨分化,并通过增强对水凝胶内分化的MSCs中alizarin red、von Kossa、碱性磷酸酶的染色,以及对骨胶原和骨钙素的免疫染色进一步验证了这一点。值得注意的是,FGFC-1显著诱导成骨分化。这些发现强调了负载fgfc -1的CMC水凝胶作为干细胞介导的骨再生在生物医学应用中的有前景的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
11.90
自引率
2.70%
发文量
1621
审稿时长
48 days
期刊介绍: Biomedicine & Pharmacotherapy stands as a multidisciplinary journal, presenting a spectrum of original research reports, reviews, and communications in the realms of clinical and basic medicine, as well as pharmacology. The journal spans various fields, including Cancer, Nutriceutics, Neurodegenerative, Cardiac, and Infectious Diseases.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信