TY - JOUR
T1 - Human blood-derived fibrin releasates
T2 - Composition and use for the culture of cell lines and human primary cells
AU - Burnouf, Thierry
AU - Lee, Chang Yu
AU - Luo, Chin Wan
AU - Kuo, Ya Po
AU - Chou, Ming Li
AU - Wu, Yu Wen
AU - Tseng, Yu Hong
AU - Su, Chen Yao
N1 - Funding Information:
This work was supported in part by the National Science Council of Taiwan (NSC-99-2811-B-038-021 ) to TB as a Foreign Specialist and as a Visiting Professor to Taipei Medical University
PY - 2012/1
Y1 - 2012/1
N2 - We have evaluated the capacity of two human blood fractions to substitute for FBS as growth medium supplement for human and animal cell cultures. Non-anticoagulated blood from volunteer donors (N = 13) was centrifuged to isolate a supernatant serum (SS) and a platelet-rich fibrin (PRF) clot which was squeezed to extract the releasate (PRFR). Both materials were characterized for the content in PDGF-AB, TGF-β1, VEGF, bFGF, EGF, IGF, total protein, albumin, IgG, IgM IgA, fibrinogen, cholesterol, triglycerides, various chemistry analytes and hemoglobin. Cell growth promoting activity of pooled SS and PRFR at 1, 5, and 10% in growth medium was evaluated over 7 days using human (HEK293, MG-63) and animal (SIRC, 3T3) cell lines and two human primary cultures (gingival fibroblasts and periodontal ligaments). Viable cell count was compared to that in cultures in FBS free-medium and 10% FBS supplement. SS and PRFR at 1-10% stimulated cell growth significantly more than FBS-free medium and in a way similar to 10% FBS in all cultures apart from 3T3. These two human blood-derived fibrin releasates are equally efficient to substitute for FBS as supplement for cell cultures and could be useful for specialized applications in regenerative medicine, dentistry and oral implantology, or cell therapy.
AB - We have evaluated the capacity of two human blood fractions to substitute for FBS as growth medium supplement for human and animal cell cultures. Non-anticoagulated blood from volunteer donors (N = 13) was centrifuged to isolate a supernatant serum (SS) and a platelet-rich fibrin (PRF) clot which was squeezed to extract the releasate (PRFR). Both materials were characterized for the content in PDGF-AB, TGF-β1, VEGF, bFGF, EGF, IGF, total protein, albumin, IgG, IgM IgA, fibrinogen, cholesterol, triglycerides, various chemistry analytes and hemoglobin. Cell growth promoting activity of pooled SS and PRFR at 1, 5, and 10% in growth medium was evaluated over 7 days using human (HEK293, MG-63) and animal (SIRC, 3T3) cell lines and two human primary cultures (gingival fibroblasts and periodontal ligaments). Viable cell count was compared to that in cultures in FBS free-medium and 10% FBS supplement. SS and PRFR at 1-10% stimulated cell growth significantly more than FBS-free medium and in a way similar to 10% FBS in all cultures apart from 3T3. These two human blood-derived fibrin releasates are equally efficient to substitute for FBS as supplement for cell cultures and could be useful for specialized applications in regenerative medicine, dentistry and oral implantology, or cell therapy.
KW - Blood
KW - Cell culture
KW - FBS
KW - Growth factors
KW - Platelet
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U2 - 10.1016/j.biologicals.2011.09.017
DO - 10.1016/j.biologicals.2011.09.017
M3 - Article
C2 - 22027351
AN - SCOPUS:84856418736
SN - 1045-1056
VL - 40
SP - 21
EP - 30
JO - Biologicals
JF - Biologicals
IS - 1
ER -