TY - JOUR
T1 - Platelet lysate as an autologous alternative for fetal bovine serum in cardiovascular tissue engineering
AU - Riem Vis, P.W.
AU - Bouten, C.V.C.
AU - Sluijter, J.P.G.
AU - Herwerden, van, L.A.
AU - Kluin, J.
PY - 2010
Y1 - 2010
N2 - There is an ongoing search for alternative tissue culture sera to engineer autologous tissues, since use of fetal bovine serum (FBS) is limited under Good Tissue Practice (GTP) guidelines. We compared FBS with human Platelet-lysate (PL) in media for in vitro cell culture. A threefold increase in duplication rate was found when human, saphenous vein-derived myofibroblasts were cultured in PL, while expression of marker proteins (a-smooth muscle actin, vimentin, desmin and non-muscle myosin heavy chain) was similar. Hsp47 mRNA-expression was increased in PL-cells and type III collagen fibers were seen on PL-cell monolayers, but not on cells cultured in FBS. These results imply a more efficient collagen fiber production. We also found higher levels of proteins involved in tissue repair and collagen remodeling, which could explain increased production of proteases and protease inhibitors by PL-cells. Our findings indicate that PL is beneficial because of the increased duplication rate, in addition to the increased matrix production and remodeling. This could lead to production of strong tissue with properly organized collagen fibers, which is important for heart valve tissue engineering.
AB - There is an ongoing search for alternative tissue culture sera to engineer autologous tissues, since use of fetal bovine serum (FBS) is limited under Good Tissue Practice (GTP) guidelines. We compared FBS with human Platelet-lysate (PL) in media for in vitro cell culture. A threefold increase in duplication rate was found when human, saphenous vein-derived myofibroblasts were cultured in PL, while expression of marker proteins (a-smooth muscle actin, vimentin, desmin and non-muscle myosin heavy chain) was similar. Hsp47 mRNA-expression was increased in PL-cells and type III collagen fibers were seen on PL-cell monolayers, but not on cells cultured in FBS. These results imply a more efficient collagen fiber production. We also found higher levels of proteins involved in tissue repair and collagen remodeling, which could explain increased production of proteases and protease inhibitors by PL-cells. Our findings indicate that PL is beneficial because of the increased duplication rate, in addition to the increased matrix production and remodeling. This could lead to production of strong tissue with properly organized collagen fibers, which is important for heart valve tissue engineering.
U2 - 10.1089/ten.TEA.2009.0331
DO - 10.1089/ten.TEA.2009.0331
M3 - Article
C2 - 19908968
SN - 1937-3341
VL - 16
SP - 1317
EP - 1327
JO - Tissue engineering. Part A
JF - Tissue engineering. Part A
IS - 4
ER -