TY - JOUR
T1 - Three-dimensional culture using human plasma-medium gel with fragmin/protamine microparticles for proliferation of various human cells
AU - Kishimoto, Satoko
AU - Ishihara, Masayuki
AU - Takikawa, Makoto
AU - Takikawa, Megumi
AU - Sumi, Yuki
AU - Nakamura, Shingo
AU - Fujita, Masanori
AU - Sato, Toshinori
AU - Kiyosawa, Tomoharu
N1 - Funding Information:
Acknowledgments This study was partially supported by the Ministry of Education, Culture, Sports, Science and Technology of Japan under Grant No. 23300181. Dr. Satoko Kishimoto was partially supported by Restart Postdoctoral (RPD) Fellowship of the Japan Society for the Promotion of Science.
Publisher Copyright:
© 2013, Springer Science+Business Media Dordrecht.
PY - 2014/10/1
Y1 - 2014/10/1
N2 - Fragmin/protamine microparticles (F/P MPs) have been used as carriers for the preservation and activation of cytokines in human plasma (HP)–Dulbecco’s modified Eagle’s medium (DMEM) gels. This study investigated a three-dimensional (3D) culture system using an HP–DMEM gel with 0.1 mg/mL F/P MPs and 5 ng/mL FGF-2 for the proliferation of human dermal fibroblast cells (DFCs), human microvascular endothelial cells (MVECs) and human coronary smooth muscle cells (SMCs), or 5 ng/mL interleukin (IL)-3/granulocyte-macrophage colony-stimulating factor (GM-CSF) for a human hematopoietic cell line (TF-1 cells). DFCs, MVECs, SMCs and TF-1 cells grew rapidly under 3D culture conditions using a low-concentration HP (2 %)–DMEM gel with F/P MPs and FGF-2 (for DFCs, MVECs and SMCs) or IL-3/GM-CSF (for TF-1 cells) at doubling times of 22, 23, 25 and 18 h, respectively, without the use of animal serum, compared to under 2D culture conditions using low-concentration human serum (2 %)–DMEM with 5 ng/mL FGF-2 or IL-3/GM-CSF on F/P MP-coated plates at doubling times of approximately 26, 25, 40 and 20 h, respectively.
AB - Fragmin/protamine microparticles (F/P MPs) have been used as carriers for the preservation and activation of cytokines in human plasma (HP)–Dulbecco’s modified Eagle’s medium (DMEM) gels. This study investigated a three-dimensional (3D) culture system using an HP–DMEM gel with 0.1 mg/mL F/P MPs and 5 ng/mL FGF-2 for the proliferation of human dermal fibroblast cells (DFCs), human microvascular endothelial cells (MVECs) and human coronary smooth muscle cells (SMCs), or 5 ng/mL interleukin (IL)-3/granulocyte-macrophage colony-stimulating factor (GM-CSF) for a human hematopoietic cell line (TF-1 cells). DFCs, MVECs, SMCs and TF-1 cells grew rapidly under 3D culture conditions using a low-concentration HP (2 %)–DMEM gel with F/P MPs and FGF-2 (for DFCs, MVECs and SMCs) or IL-3/GM-CSF (for TF-1 cells) at doubling times of 22, 23, 25 and 18 h, respectively, without the use of animal serum, compared to under 2D culture conditions using low-concentration human serum (2 %)–DMEM with 5 ng/mL FGF-2 or IL-3/GM-CSF on F/P MP-coated plates at doubling times of approximately 26, 25, 40 and 20 h, respectively.
KW - 3D culture
KW - Cytokine carrier
KW - Fragmin/protamine microparticles (F/P MPs)
KW - Plasma–medium gel
UR - http://www.scopus.com/inward/record.url?scp=84881419418&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84881419418&partnerID=8YFLogxK
U2 - 10.1007/s10616-013-9628-5
DO - 10.1007/s10616-013-9628-5
M3 - Article
AN - SCOPUS:84881419418
SN - 0920-9069
VL - 66
SP - 791
EP - 802
JO - Cytotechnology
JF - Cytotechnology
IS - 5
ER -