“…Therefore, therapeutic application of MSCs should be reconsidered in terms of the tissue source of these cells, the methods of isolation and the cell culture conditions that markedly modulate their biological properties and behavior. For example, CB-, BM-, Wharton's jelly-, placenta-, amniotic fluid/ membrane-and AT-derived MSCs differ with respect to their vasculogenic regulatory/stimulating capacity, adipogenic, bone or cartilage differentiation potential and other immunomodulatory functions such as the inhibition of T cell mitogenesis [da Silva Meirelles et al, 2006;Karagianni et al, 2013;Ketterl et al, 2015;Marquez-Curtis et al, 2015;Schäfer and Bieback, 2016]. In addition, the culture conditions of MSCs and preservation modes for their future use in therapeutic strategies should be standardized in order to determine the activities required, including those supporting or modulating/inhibiting vasculogenesis [Kang et al, 2011;Bieback, 2013;Kinzebach and Bieback, 2013].…”