Effects of Oral Cavity Stem Cell Sources and Serum-Free Cell Culture on Hydrogel Encapsulation of Mesenchymal Stem Cells for Bone Regeneration: An In Vitro Investigation

被引:3
|
作者
Arpornmaeklong, Premjit [1 ]
Boonyuen, Supakorn [2 ]
Apinyauppatham, Komsan [1 ]
Pripatnanont, Prisana [3 ]
机构
[1] Thammasat Univ, Fac Dent, Rangsit Campus, Pathum Thani 12121, Thailand
[2] Thammasat Univ, Fac Sci & Technol, Dept Chem, Rangsit Campus, Pathum Thani 12121, Thailand
[3] Prince Songkla Univ, Fac Dent, Hat Yai 90110, Thailand
来源
BIOENGINEERING-BASEL | 2024年 / 11卷 / 01期
关键词
adipose stem cells; buccal fat pad; dental pulp stem cells; hydrogel cell encapsulation; periodontal ligament stem cells; serum-free condition; oral cavity stem cells; oral and maxillofacial osteogenesis and bone regeneration;
D O I
10.3390/bioengineering11010059
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: To develop a stem cell delivery model and improve the safety of stem cell transplantation for bone regeneration, this study aimed to determine the effects of stem cell sources, serum-free cell culture, and hydrogel cell encapsulation on the growth and osteogenic differentiation of mesenchymal stem cells (MSCs) from the oral cavity. Methods: The study groups were categorized according to stem cell sources into buccal fat pad adipose (hBFP-ADSCs) (Groups 1, 4, and 7), periodontal ligament (hPDLSCs) (Groups 2, 5, and 8), and dental pulp-derived stem cells (hDPSCs) (Groups 3, 6, and 9). MSCs from each source were isolated and expanded in three types of sera: fetal bovine serum (FBS) (Groups 1-3), human serum (HS) (Groups 4-6), and synthetic serum (SS) (StemPro (TM) MSC SFM) (Groups 7-9) for monolayer (m) and hydrogel cell encapsulation cultures (e). Following this, the morphology, expression of MSC cell surface antigens, growth, and osteogenic differentiation potential of the MSCs, and the expression of adhesion molecules were analyzed and compared. Results: SS decreased variations in the morphology and expression levels of cell surface antigens of MSCs from three cell sources (Groups 7m-9m). The levels of osteoblastic differentiation of the hPDLSCs and hBFP-ADSCs were increased in SS (Groups 8m and 7m) and the cell encapsulation model (Groups 1e, 4e, 7e-9e), but the promoting effects of SS were decreased in a cell encapsulation model (Groups 7e-9e). The expression levels of the alpha v beta 3 (ITG-alpha V beta 3) and beta 1 (ITG-beta 1) integrins in the encapsulated cells in FBS (Group 1e) were higher than those in the SS (Group 7e). Conclusions: Human PDLSCs and BFP-ADSCs were the optimum stem cell source for stem cell encapsulation by using nanohydroxyapatite-calcium carbonate microcapsule-chitosan/collagen hydrogel in serum-free conditions.
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页数:20
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