TY - JOUR
T1 - Immunomodulatory properties of porcine, bone marrow-derived multipotent mesenchymal stromal cells and comparison with their human counterpart
AU - Comite, P
AU - Cobianchi, L
AU - Avanzini, M A
AU - Mantelli, M
AU - Achille, V
AU - Zonta, S
AU - Ferrari, C
AU - Alessiani, M
AU - De Silvestri, A
AU - Gandolfo, G M
AU - Inverardi, L
AU - Brescia, L
AU - Pietrabissa, A
AU - Dionigi, P
AU - Locatelli, Franco
AU - Bernardo, M E
PY - 2011
Y1 - 2011
N2 - : Thanks to their immunonodulatory properties, multipotent mesenchymal stromal cells (MSCs) are a promising strategy for preventing/reducing the risk of graft rejection after hematopoietic cell and solid organ transplantation. We have previously demonstrated that porcine MSCs (pMSCs) can be isolated from bone marrow and display similar morphology and differentiative capacity as compared to human MSC (hMSCs). In this study, we investigated the in vitro immunomodulatory properties (namely the ability to suppress lymphocyte proliferation in response to phytohemagglutinin and the cytokine production in the culture supernatants) of pMSCs from six Large White 6-month old piglets. Similarly to hMSCs, pMSCs reduced the phytohemagglutinin-induced lymphocyte proliferation. High levels of IL-6 were found in culture supernatants, whereas IL-10 and TGF-β were not detectable. In conclusion, ex vivo expanded pMSCs share selected biological/functional properties with hMSCs. pMSCs may be used in in vivo models to investigate novel approaches of prevention of graft rejection in solid organ transplantation.
AB - : Thanks to their immunonodulatory properties, multipotent mesenchymal stromal cells (MSCs) are a promising strategy for preventing/reducing the risk of graft rejection after hematopoietic cell and solid organ transplantation. We have previously demonstrated that porcine MSCs (pMSCs) can be isolated from bone marrow and display similar morphology and differentiative capacity as compared to human MSC (hMSCs). In this study, we investigated the in vitro immunomodulatory properties (namely the ability to suppress lymphocyte proliferation in response to phytohemagglutinin and the cytokine production in the culture supernatants) of pMSCs from six Large White 6-month old piglets. Similarly to hMSCs, pMSCs reduced the phytohemagglutinin-induced lymphocyte proliferation. High levels of IL-6 were found in culture supernatants, whereas IL-10 and TGF-β were not detectable. In conclusion, ex vivo expanded pMSCs share selected biological/functional properties with hMSCs. pMSCs may be used in in vivo models to investigate novel approaches of prevention of graft rejection in solid organ transplantation.
KW - N/A
KW - N/A
UR - https://publicatt.unicatt.it/handle/10807/249196
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=84856615062&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84856615062&origin=inward
U2 - 10.1170/185
DO - 10.1170/185
M3 - Article
SN - 0145-5680
VL - 57
SP - 1600
EP - 1605
JO - Cellular and Molecular Biology
JF - Cellular and Molecular Biology
IS - suppl 57
ER -