Characterization of Biological Properties of Dental Pulp Stem Cells Grown on an Electrospun Poly(l-lactide-co-caprolactone) Scaffold

被引:8
作者
Bar, Julia K. [1 ]
Kowalczyk, Tomasz [2 ]
Grelewski, Piotr G. [1 ]
Stamnitz, Sandra [3 ]
Paprocka, Maria [3 ]
Lis, Joanna [4 ]
Lis-Nawara, Anna [1 ]
An, Seongpil [5 ,6 ]
Klimczak, Aleksandra [3 ]
机构
[1] Med Univ, Dept Immunopathol & Mol Biol, Bujwida 44, PL-50345 Wroclaw, Poland
[2] Polish Acad Sci, Inst Fundamental Technol Res IPPT PAN, Lab Polymers & Biomat, Adolfa Pawinskiego 5B St, PL-02106 Warsaw, Poland
[3] Polish Acad Sci, Hirszfeld Inst Immunol & Expt Therapy, Lab Biol Stem & Neoplast Cells, R Weigla 12, PL-53114 Wroclaw, Poland
[4] Med Univ, Dept Maxillofacial Orthopaed & Orthodont, Krakowska 26, PL-50425 Wroclaw, Poland
[5] Sungkyunkwan Univ SKKU, Dept Nano Engn, Suwon 16419, South Korea
[6] Sungkyunkwan Univ SKKU, SKKU Adv Inst Nanotechnol SAINT, Suwon 16419, South Korea
关键词
hDPSCs; poly(l-lactide-co-caprolactone); electrospun scaffold; biocompatibility; adhesion; proliferation; osteogenic differentiation; tissue engineering; EXFOLIATED DECIDUOUS TEETH; IN-VITRO; OSTEOGENIC DIFFERENTIATION; REGENERATION; ACID;
D O I
10.3390/ma15051900
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Poly(l-lactide-co-caprolactone) (PLCL) electrospun scaffolds with seeded stem cells have drawn great interest in tissue engineering. This study investigated the biological behavior of human dental pulp stem cells (hDPSCs) grown on a hydrolytically-modified PLCL nanofiber scaffold. The hDPSCs were seeded on PLCL, and their biological features such as viability, proliferation, adhesion, population doubling time, the immunophenotype of hDPSCs and osteogenic differentiation capacity were evaluated on scaffolds. The results showed that the PLCL scaffold significantly supported hDPSC viability/proliferation. The hDPSCs adhesion rate and spreading onto PLCL increased with time of culture. hDPSCs were able to migrate inside the PLCL electrospun scaffold after 7 days of seeding. No differences in morphology and immunophenotype of hDPSCs grown on PLCL and in flasks were observed. The mRNA levels of bone-related genes and their proteins were significantly higher in hDPSCs after osteogenic differentiation on PLCL compared with undifferentiated hDPSCs on PLCL. These results showed that the mechanical properties of a modified PLCL mat provide an appropriate environment that supports hDPSCs attachment, proliferation, migration and their osteogenic differentiation on the PLCL scaffold. The good PLCL biocompatibility with dental pulp stem cells indicates that this mat may be applied in designing a bioactive hDPSCs/PLCL construct for bone tissue engineering.
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页数:28
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