Novel Chitosan-Gelatin Scaffold with Valproic Acid Augments In Vitro Osteoblast Differentiation of Mesenchymal Stem Cells

被引:1
作者
Alghofaily, Maha [1 ]
Alsalleeh, Fahd [1 ]
Alssum, Lamees [2 ]
Muthurangan, Manikandan [3 ]
Alfayez, Musaad [3 ]
Weir, Michael D. [4 ]
Xu, Hockin H. K. [4 ]
机构
[1] King Saud Univ, Coll Dent, Restorat Dent Sci, Riyadh 11541, Saudi Arabia
[2] King Saud Univ, Coll Dent, Dept Periodont & Community Dent, Riyadh 11545, Saudi Arabia
[3] King Saud Univ, Coll Med, Dept Anat, Stem Cell Unit, Riyadh 11461, Saudi Arabia
[4] Univ Maryland, Sch Dent, Dept Biomat & Regenerat Dent Med, Baltimore, MD 21201 USA
关键词
chitosan; gelatin; scaffolds; histone deacetylase inhibitors; stem cells; HISTONE; PROLIFERATION;
D O I
10.3390/jfb15090252
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The study aimed to develop a biodegradable scaffold incorporating valproic acid (VPA) for improved human bone marrow-derived mesenchymal stem cell (hBMSC) proliferation, differentiation, and bone mineral synthesis. A chitosan-gelatin (CH-G) scaffold was fabricated and loaded with varying concentrations of VPA (1, 3, 5 mM/L). In vitro studies assessed drug release, cell proliferation, morphology, mineralization, and gene expression. VPA was rapidly released from the scaffold, with over 90% cumulative release within seven days. Cells cultured on VPA-loaded scaffolds exhibited significantly enhanced proliferation and mineralization compared to the control. VPA treatment upregulated osteocalcin and runt-related transcription factor 2 (Runx-2) expression, key markers of osteogenic differentiation. The CH-G scaffold, particularly with 1 mM/L VPA, demonstrates excellent biocompatibility and promotes hBMSC-mediated bone regeneration. This novel approach holds promise for future applications in bone tissue engineering.
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页数:13
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