TY - JOUR
T1 - Practical and functional culture technologies for primary hepatocytes
AU - Ijima, Hiroyuki
N1 - Funding Information:
This work was supported in part by a Grant-in-Aid for Scientific Research (B): 18360399 from the Ministry of Education, Culture, Sports, Science and Technology of Japan .
PY - 2010/2/15
Y1 - 2010/2/15
N2 - The liver is a central organ for metabolism in the body, and it is therefore important to develop effective culture methods for the expression of liver-specific functions. The development of effective primary hepatocyte culture methods for the expression of these functions has been attempted by focusing on cell-cell and cell-matrix interactions. Two-dimensional organoid culture methods using substrata with the immobilized arginine-glycine-aspartic acid sequence, a well-known cell-adhesive sequence, have been developed. Furthermore, a drug metabolism simulator and a hybrid-type blood purification system as applications of this type of two-dimensional organoid culture method have been developed. On the other hand, growth factor/heparin-immobilized culture substrata and cell-embedded hydrogels in extracellular matrix-filled biocompatible macroporous scaffold culture systems for liver tissue engineering have been developed. Promotion of organoid formation and high expression of the liver-specific functions of primary rat hepatocytes will be realized by using these substrata and culture systems.
AB - The liver is a central organ for metabolism in the body, and it is therefore important to develop effective culture methods for the expression of liver-specific functions. The development of effective primary hepatocyte culture methods for the expression of these functions has been attempted by focusing on cell-cell and cell-matrix interactions. Two-dimensional organoid culture methods using substrata with the immobilized arginine-glycine-aspartic acid sequence, a well-known cell-adhesive sequence, have been developed. Furthermore, a drug metabolism simulator and a hybrid-type blood purification system as applications of this type of two-dimensional organoid culture method have been developed. On the other hand, growth factor/heparin-immobilized culture substrata and cell-embedded hydrogels in extracellular matrix-filled biocompatible macroporous scaffold culture systems for liver tissue engineering have been developed. Promotion of organoid formation and high expression of the liver-specific functions of primary rat hepatocytes will be realized by using these substrata and culture systems.
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U2 - 10.1016/j.bej.2009.10.003
DO - 10.1016/j.bej.2009.10.003
M3 - Review article
AN - SCOPUS:75349100577
SN - 1369-703X
VL - 48
SP - 332
EP - 336
JO - Biochemical Engineering Journal
JF - Biochemical Engineering Journal
IS - 3
ER -