Low Molecular Weight Hyaluronic Acid Effect on Dental Pulp Stem Cells In Vitro

被引:20
|
作者
Schmidt, Jan [1 ,2 ]
Pilbauerova, Nela [1 ,2 ]
Soukup, Tomas [3 ]
Suchankova-Kleplova, Tereza [1 ,2 ]
Suchanek, Jakub [1 ,2 ]
机构
[1] Charles Univ Prague, Fac Med Hradec Kralove, Dept Dent, Hradec Kralove 50005, Czech Republic
[2] Univ Hosp, Hradec Kralove 50005, Czech Republic
[3] Charles Univ Prague, Fac Med Hradec Kralove, Dept Histol & Embryol, Hradec Kralove 50003, Czech Republic
关键词
hyaluronic acid; dental pulp stem cells; low molecular weight hyaluronic acid; tissue engineering; scaffold;
D O I
10.3390/biom11010022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hyaluronic acid (HA) and dental pulp stem cells (DPSCs) are attractive research topics, and their combined use in the field of tissue engineering seems to be very promising. HA is a natural extracellular biopolymer found in various tissues, including dental pulp, and due to its biocompatibility and biodegradability, it is also a suitable scaffold material. However, low molecular weight (LMW) fragments, produced by enzymatic cleavage of HA, have different bioactive properties to high molecular weight (HMW) HA. Thus, the impact of HA must be assessed separately for each molecular weight fraction. In this study, we present the effect of three LMW-HA fragments (800, 1600, and 15,000 Da) on DPSCs in vitro. Discrete biological parameters such as DPSC viability, morphology, and cell surface marker expression were determined. Following treatment with LMW-HA, DPSCs initially presented with an acute reduction in proliferation (p < 0.0016) and soon recovered in subsequent passages. They displayed significant size reduction (p = 0.0078, p = 0.0019, p = 0.0098) while maintaining high expression of DPSC markers (CD29, CD44, CD73, CD90). However, in contrast to controls, a significant phenotypic shift (p < 0.05; CD29, CD34, CD90, CD106, CD117, CD146, CD166) of surface markers was observed. These findings provide a basis for further detailed investigations and present a strong argument for the importance of HA scaffold degradation kinetics analysis.
引用
收藏
页码:1 / 16
页数:16
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