Detail
Article
Online article
FT
Medvik - BMC
  • Something wrong with this record ?

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

J. Schmidt, N. Pilbauerova, T. Soukup, T. Suchankova-Kleplova, J. Suchanek

. 2020 ; 11 (1) : . [pub] 20201228

Language English Country Switzerland

Document type Journal Article, Research Support, Non-U.S. Gov't

Grant support
Progres Q40/06 Univerzita Karlova v Praze - International
Progres Q40/13 Univerzita Karlova v Praze - International

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.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc21019615
003      
CZ-PrNML
005      
20210830101213.0
007      
ta
008      
210728s2020 sz f 000 0|eng||
009      
AR
024    7_
$a 10.3390/biom11010022 $2 doi
035    __
$a (PubMed)33379324
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a sz
100    1_
$a Schmidt, Jan $u Department of Dentistry, Charles University, Faculty of Medicine in Hradec Kralove and University Hospital, 500 05 Hradec Kralove, Czech Republic
245    10
$a Low Molecular Weight Hyaluronic Acid Effect on Dental Pulp Stem Cells In Vitro / $c J. Schmidt, N. Pilbauerova, T. Soukup, T. Suchankova-Kleplova, J. Suchanek
520    9_
$a 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.
650    _2
$a buněčná diferenciace $x účinky léků $7 D002454
650    _2
$a proliferace buněk $x účinky léků $7 D049109
650    _2
$a kultivované buňky $7 D002478
650    _2
$a zubní dřeň $x účinky léků $x růst a vývoj $7 D003782
650    _2
$a lidé $7 D006801
650    _2
$a kyselina hyaluronová $x farmakologie $7 D006820
650    _2
$a molekulová hmotnost $7 D008970
650    _2
$a kmenové buňky $x cytologie $x účinky léků $7 D013234
650    _2
$a tkáňové inženýrství $7 D023822
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Pilbauerova, Nela $u Department of Dentistry, Charles University, Faculty of Medicine in Hradec Kralove and University Hospital, 500 05 Hradec Kralove, Czech Republic
700    1_
$a Soukup, Tomas $u Department of Histology and Embryology, Charles University, Faculty of Medicine in Hradec Kralove, 500 03 Hradec Králové, Czech Republic
700    1_
$a Suchankova-Kleplova, Tereza $u Department of Dentistry, Charles University, Faculty of Medicine in Hradec Kralove and University Hospital, 500 05 Hradec Kralove, Czech Republic
700    1_
$a Suchanek, Jakub $u Department of Dentistry, Charles University, Faculty of Medicine in Hradec Kralove and University Hospital, 500 05 Hradec Kralove, Czech Republic
773    0_
$w MED00188737 $t Biomolecules $x 2218-273X $g Roč. 11, č. 1 (2020)
856    41
$u https://pubmed.ncbi.nlm.nih.gov/33379324 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y p $z 0
990    __
$a 20210728 $b ABA008
991    __
$a 20210830101214 $b ABA008
999    __
$a ok $b bmc $g 1690439 $s 1140061
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2020 $b 11 $c 1 $e 20201228 $i 2218-273X $m Biomolecules $n Biomolecules $x MED00188737
GRA    __
$a Progres Q40/06 $p Univerzita Karlova v Praze $2 International
GRA    __
$a Progres Q40/13 $p Univerzita Karlova v Praze $2 International
LZP    __
$a Pubmed-20210728

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...