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Application of whey protein isolate in bone regeneration: Effects on growth and osteogenic differentiation of bone-forming cells

  1. 1.
    SYSNO ASEP0489871
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleApplication of whey protein isolate in bone regeneration: Effects on growth and osteogenic differentiation of bone-forming cells
    Author(s) Douglas, T.E.L. (BE)
    Vandrovcová, Marta (FGU-C) RID, ORCID
    Kročilová, Nikola (FGU-C)
    Keppler, J. K. (DE)
    Zárubová, Jana (FGU-C) RID, ORCID
    Skirtach, A. G. (BE)
    Bačáková, Lucie (FGU-C) RID, ORCID
    Source TitleJournal of Dairy Science. - : Elsevier - ISSN 0022-0302
    Roč. 101, č. 1 (2018), s. 28-36
    Number of pages9 s.
    Languageeng - English
    CountryUS - United States
    Keywordswhey protein isolate ; cell proliferation ; osteogenic differentiation ; adipose-derived stem cell
    Subject RIVEI - Biotechnology ; Bionics
    OECD categoryBiomaterials (as related to medical implants, devices, sensors)
    R&D ProjectsNV15-33018A GA MZd - Ministry of Health (MZ)
    Institutional supportFGU-C - RVO:67985823
    UT WOS000418498800003
    EID SCOPUS85034433045
    DOI10.3168/jds.2017-13119
    AnnotationRecently, milk-derived proteins have attracted attention for applications in the biomedical field such as tissue regeneration. Whey protein isolate (WPI), especially its main component beta-lactoglobulin, can modulate immunity and acts as an antioxidant, antitumor, antiviral, and antibacterial agent. There are very few reports of the application of WPI in tissue engineering, especially in bone tissue engineering. In this study, we tested the influence of different concentrations of WPI on behavior of human osteoblast-like Saos-2 cells, human adipose tissue-derived stem cells (ASC), and human neonatal dermal fibroblasts (FIB ). The positive effect on growth was apparent for Saos-2 cells and FIB but not for ASC. However, the expression of markers characteristic for early osteogenic cell differentiation [type-I collagen (COLT) and alkaline phosphatase (ALP)] as well as ALP activity, increased dose-dependently in ASC. Importantly, Saos-2 cells were able to deposit calcium in the presence of WPI, even in a proliferation medium without other supplements that support osteogenic cell differentiation. The results indicate that, depending on the cell type, WPI can act as an enhancer of cell proliferation and osteogenic differentiation. Therefore, enrichment of biomaterials for bone regeneration with WPI seems a promising approach, especially due to the low cost of WPI.
    WorkplaceInstitute of Physiology
    ContactLucie Trajhanová, lucie.trajhanova@fgu.cas.cz, Tel.: 241 062 400
    Year of Publishing2019
Number of the records: 1  

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