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Short Pretreatment with Calcitriol Is Far Superior to Continuous Treatment in Stimulating Proliferation and Osteogenic Differentiation of Human Adipose Stem Cells

OBJECTIVE: This study investigated whether short stimulation (30 minutes) of human adipose stem cells (hASCs) with 1,25-dihydroxyvitamin D3(calcitriol or 1,25-(OH)(2)VitD(3)), fitting within the surgical procedure time frame, suffices to induce osteogenic differentiation, and compared this with cont...

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Detalles Bibliográficos
Autores principales: Mokhtari-Jafari, Fatemeh, Amoabediny, Ghassem, Dehghan, Mohammad Mehdi, Helder, Marco N., Zandieh-Doulabi, Behrouz, Klein-Nulend, Jenneke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royan Institute 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6947014/
https://www.ncbi.nlm.nih.gov/pubmed/31863654
http://dx.doi.org/10.22074/cellj.2020.6773
Descripción
Sumario:OBJECTIVE: This study investigated whether short stimulation (30 minutes) of human adipose stem cells (hASCs) with 1,25-dihydroxyvitamin D3(calcitriol or 1,25-(OH)(2)VitD(3)), fitting within the surgical procedure time frame, suffices to induce osteogenic differentiation, and compared this with continuous treatment with 1,25-(OH)(2)VitD(3). MATERIALS AND METHODS: In this experimental study, hASCs were pretreated with/without 10 nM calcitriol for 30 minutes, seeded on biphasic calcium phosphate (BCP), and cultured for 3 weeks with/without 1,25-(OH)(2)VitD(3). Cell attachment was determined 30 minutes after cell seeding. AlamarBlue assay, alkaline phosphatase (ALP) assay, ALP staining, real-time polymerase chain reaction (PCR), and protein assay were used to evaluate the effect of short calcitriol pretreatment on proliferation and osteogenic differentiation of hASCs up to 3 weeks. RESULTS: Pretreatment with 1,25-(OH)(2)VitD(3)enhanced the attachment of hASCs to BCP by 1.5-fold compared to non- treated cells and increased the proliferation by 3.5-fold at day 14, and 2.6-fold at day 21. In contrast, continuous treatment increased the proliferation by 1.7-fold only at day 14. After 2 weeks, ALP activity was increased by 18.5-fold when hASCs were pretreated with 1,25-(OH)(2)VitD(3)for 30 minutes but increased only 2.6-fold when compared with its continuous counterpart. Moreover, after 14 days, pretreatment resulted in significant upregulation of the osteogenic markers RUNX2 and SPARC by 3.6-fold and 2.2-fold, respectively, while this was not observed upon continuous treatment. Finally, 30 minutes pretreatment of hASCs with 1,25-(OH)(2)VitD(3)increased VEGF(189) expression, which may contribute to the process of angiogenesis. CONCLUSION: This study is the first research showing that 30 minutes pretreatment of hASCs with 1,25-(OH)(2)VitD(3), not only enhanced cell attachment to the scaffold at seeding time, but also promoted the proliferation and osteogenic differentiation of hASCs more strongly than continuous treatment, suggesting that short pre-treatment with 1,25-(OH)(2)VitD(3)is a promising approach for the regeneration of bones in a one-step surgical procedure.