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Dental pulp stem cell-derived extracellular matrix: autologous tool boosting bone regeneration.
Alksne, Milda; Kalvaityte, Migle; Simoliunas, Egidijus; Gendviliene, Ieva; Barasa, Povilas; Rinkunaite, Ieva; Kaupinis, Algirdas; Seinin, Dmitrij; Rutkunas, Vygandas; Bukelskiene, Virginija.
  • Alksne M; Institute of Biochemistry, Life Sciences Center, Vilnius University, Vilnius, Lithuania. Electronic address: milda.peciukaityte@gf.vu.lt.
  • Kalvaityte M; Institute of Biochemistry, Life Sciences Center, Vilnius University, Vilnius, Lithuania.
  • Simoliunas E; Institute of Biochemistry, Life Sciences Center, Vilnius University, Vilnius, Lithuania.
  • Gendviliene I; Institute of Odontology, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
  • Barasa P; Institute of Biochemistry, Life Sciences Center, Vilnius University, Vilnius, Lithuania.
  • Rinkunaite I; Institute of Biochemistry, Life Sciences Center, Vilnius University, Vilnius, Lithuania.
  • Kaupinis A; Institute of Biochemistry, Life Sciences Center, Vilnius University, Vilnius, Lithuania.
  • Seinin D; National Center of Pathology, Affiliate of Vilnius University Hospital Santaros Klinikos, Vilnius, Lithuania.
  • Rutkunas V; Institute of Odontology, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
  • Bukelskiene V; Institute of Biochemistry, Life Sciences Center, Vilnius University, Vilnius, Lithuania.
Cytotherapy ; 24(6): 597-607, 2022 06.
Article en En | MEDLINE | ID: mdl-35304075
ABSTRACT
BACKGROUND

AIMS:

To facilitate artificial bone construct integration into a patient's body, scaffolds are enriched with different biologically active molecules. Among various scaffold decoration techniques, coating surfaces with cell-derived extracellular matrix (ECM) is a rapidly growing field of research. In this study, for the first time, this technology was applied using primary dental pulp stem cells (DPSCs) and tested for use in artificial bone tissue construction.

METHODS:

Rat DPSCs were grown on three-dimensional-printed porous polylactic acid scaffolds for 7 days. After the predetermined time, samples were decellularized, and the remaining ECM detailed proteomic analysis was performed. Further, DPSC-secreated ECM impact to mesenchymal stromal cells (MSC) behaviour as well as its role in osteoregeneration induction were analysed.

RESULTS:

It was identified that DPSC-specific ECM protein network ornamenting surface-enhanced MSC attachment, migration and proliferation and even promoted spontaneous stem cell osteogenesis. This protein network also demonstrated angiogenic properties and did not stimulate MSCs to secrete molecules associated with scaffold rejection. With regard to bone defects, DPSC-derived ECM recruited endogenous stem cells, initiating the bone self-healing process. Thus, the DPSC-secreted ECM network was able to significantly enhance artificial bone construct integration and induce successful tissue regeneration.

CONCLUSIONS:

DPSC-derived ECM can be a perfect tool for decoration of various biomaterials in the context of bone tissue engineering.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteómica / Andamios del Tejido Límite: Animals Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteómica / Andamios del Tejido Límite: Animals Idioma: En Año: 2022 Tipo del documento: Article