TY - JOUR
T1 - Hybrid sponge comprised of galactosylated chitosan and hyaluronic acid mediates the co-culture of hepatocytes and endothelial cells
AU - Shang, Yi
AU - Tamai, Miho
AU - Ishii, Ryusei
AU - Nagaoka, Noriyuki
AU - Yoshida, Yasuhiro
AU - Ogasawara, Masamichi
AU - Yang, Jun
AU - Tagawa, Yoh ichi
N1 - Funding Information:
This study was supported by a Grant-in-Aid for Challenging Exploratory Research (no. 24650254 ) from the Japan Society for the Promotion of Science (JSPS) and a Grant-in-Aid for Scientific Research on Innovative Areas (no. 231190003 ) from the Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan. Yi Shang received the MEXT Scholarship from Japanese Government. We also thank all members of our laboratory for their excellent animal care.
PY - 2014/1
Y1 - 2014/1
N2 - When constructing an in vitro model of liver tissue to mimic the in vivo liver microenvironment, the major challenge is to preserve and maintain the hepatocyte phenotype. The aim of this study was to develop a novel intelligent hybrid sponge for use in a dense co-culture system designed to simulate the liver microenvironment. We prepared a galactosylated chitosan (GCs)/hyaluronic acid (HA) hybrid sponge using a freeze-drying technique for the co-culture of primary hepatocytes and endothelial cells. Subsequently, we investigated the biocompatibility of the GCs/HA scaffold with primary hepatocytes and endothelial cells in terms of cell attachment, morphology, bioactivity, and maintenance of specific liver functions. The GCs/HA-hybrid sponge demonstrated good biocompatibility not only with primary hepatocytes, but also with endothelial cells. In our model, primary hepatocytes exhibited superior bioactivity and higher levels of liver-specific functions in terms of hepatocyte-specific gene expression, urea production, and testosterone metabolism as compared to a monoculture system. We succeeded in constructing a liver tissue-like model using the GCs/HA-hybrid sponge. Therefore, we anticipate that GCs/HA-hybrid sponges may be a promising matrix for the co-culture of hepatocytes and endothelial cells in liver tissue engineering, and might be employed as a novel co-culture model for applications in toxicology and drug metabolism.
AB - When constructing an in vitro model of liver tissue to mimic the in vivo liver microenvironment, the major challenge is to preserve and maintain the hepatocyte phenotype. The aim of this study was to develop a novel intelligent hybrid sponge for use in a dense co-culture system designed to simulate the liver microenvironment. We prepared a galactosylated chitosan (GCs)/hyaluronic acid (HA) hybrid sponge using a freeze-drying technique for the co-culture of primary hepatocytes and endothelial cells. Subsequently, we investigated the biocompatibility of the GCs/HA scaffold with primary hepatocytes and endothelial cells in terms of cell attachment, morphology, bioactivity, and maintenance of specific liver functions. The GCs/HA-hybrid sponge demonstrated good biocompatibility not only with primary hepatocytes, but also with endothelial cells. In our model, primary hepatocytes exhibited superior bioactivity and higher levels of liver-specific functions in terms of hepatocyte-specific gene expression, urea production, and testosterone metabolism as compared to a monoculture system. We succeeded in constructing a liver tissue-like model using the GCs/HA-hybrid sponge. Therefore, we anticipate that GCs/HA-hybrid sponges may be a promising matrix for the co-culture of hepatocytes and endothelial cells in liver tissue engineering, and might be employed as a novel co-culture model for applications in toxicology and drug metabolism.
KW - Endothelial cell
KW - Galactosylated chitosan
KW - Hyaluronic acid
KW - Liver
KW - Primary hepatocyte
KW - Tissue
UR - http://www.scopus.com/inward/record.url?scp=84890128037&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84890128037&partnerID=8YFLogxK
U2 - 10.1016/j.jbiosc.2013.06.015
DO - 10.1016/j.jbiosc.2013.06.015
M3 - Article
C2 - 23896016
AN - SCOPUS:84890128037
SN - 1389-1723
VL - 117
SP - 99
EP - 106
JO - Journal of Bioscience and Bioengineering
JF - Journal of Bioscience and Bioengineering
IS - 1
ER -