A method for the effective formation of hepatocyte spheroids using a biodegradable polymer nanosphere

被引:8
作者
Gwak, So-Jung
Choi, Dongho
Paik, Seung Sam
Cho, Seung-Woo
Kim, Sang-Soo
Choi, Cha Yong
Kim, Byung-Soo [1 ]
机构
[1] Hanyang Univ, Dept Bioengn, Seoul 133791, South Korea
[2] Seoul Natl Univ, Interdisciplinary Program Biochem Engn & Biotechn, Seoul, South Korea
[3] Hanyang Univ, Coll Engn, Dept Chem Engn, Seoul 133791, South Korea
[4] Soonchunhyang Univ, Coll Med, Dept Surg, Seoul, South Korea
[5] Hanyang Univ, Coll Med, Dept Surg, Seoul 133791, South Korea
[6] Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 151, South Korea
关键词
hepatocyte; poly(lactide-co-glycolide) nanosphere; spheroid;
D O I
10.1002/jbm.a.30687
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Cultures of hepatocytes in spheroid form are known to maintain higher cell viability and exhibit better hepatocyte functions than those in monolayer cultures. In this study, a method for the formation of hepatocyte spheroids was developed using biodegradable polymer nanospheres. The addition of poly(lactic-co-glycolic acid) nanospheres to hepatocyte cultures in spinner flasks increased the efficiency of hepatocyte spheroid formation (the number of cells in spheroids divided by the total cell number) as compared with hepatocyte cultures without nanospheres (control). The viability and mitochondrial activity of the hepatocyte spheroids in the nanosphere-added cultures were significantly higher than those in the control. In addition, the mRNA expression levels of albumin and phenylalanine hydroxylase, both of which are hepatocyte-specific proteins, were significantly higher in the nanosphere-added cultures than in the control. This new culture method improves upon the conventional method of forming hepatocyte spheroids in terms of spheroid formation efficiency, cell viability, and hepatocyte function. (c) 2006 Wiley Periodicals, Inc.
引用
收藏
页码:268 / 275
页数:8
相关论文
共 32 条
[1]
Dexamethasone effects on rat hepatocyte spheroid formation and function [J].
Abu-Absi, SF ;
Hu, WS ;
Hansen, LK .
TISSUE ENGINEERING, 2005, 11 (3-4) :415-426
[2]
Structural polarity and functional bile canaliculi in rat hepatocyte spheroids [J].
Abu-Absi, SF ;
Friend, JR ;
Hansen, LK ;
Hu, WS .
EXPERIMENTAL CELL RESEARCH, 2002, 274 (01) :56-67
[3]
Borel Rinkes IH, 1992, CELL TRANSPLANT, V1, P281
[4]
TOXICITY DETERMINED INVITRO BY MORPHOLOGICAL ALTERATIONS AND NEUTRAL RED ABSORPTION [J].
BORENFREUND, E ;
PUERNER, JA .
TOXICOLOGY LETTERS, 1985, 24 (2-3) :119-124
[5]
Bioartificial liver support devices: Historical perspectives [J].
Court, FG ;
Wemyss-Holden, SA ;
Dennison, AR ;
Maddern, GJ .
ANZ JOURNAL OF SURGERY, 2003, 73 (09) :739-748
[6]
Hybrid artificial liver using hepatocyte organoid culture [J].
Funatsu, K ;
Ijima, H ;
Nakazawa, K ;
Yamashita, Y ;
Shimada, M ;
Sugimachi, K .
ARTIFICIAL ORGANS, 2001, 25 (03) :194-200
[7]
Modeling mass transfer in hepatocyte spheroids via cell viability, spheroid size, and hepatocellular functions [J].
Glicklis, R ;
Merchuk, JC ;
Cohen, S .
BIOTECHNOLOGY AND BIOENGINEERING, 2004, 86 (06) :672-680
[8]
Expression of cell adhesion molecule and albumin genes in primary culture of rat hepatocytes [J].
Hou, DX ;
Arimura, M ;
Fukuda, M ;
Oka, T ;
Fujii, M .
CELL BIOLOGY INTERNATIONAL, 2001, 25 (03) :239-244
[9]
DISTRIBUTION OF PHENYLALANINE-HYDROXYLASE (EC-1.14.3.1) IN LIVER AND KIDNEY OF VERTEBRATES [J].
HSIEH, MC ;
BERRY, HK .
JOURNAL OF EXPERIMENTAL ZOOLOGY, 1979, 208 (02) :161-167
[10]
Hybrid bioartificial liver: Establishing a reversibly immortalized human hepatocyte line and developing a bioartificial liver for practical use [J].
Naoya Kobayashi ;
Teru Okitsu ;
Shuhei Nakaji ;
Noriaki Tanaka .
Journal of Artificial Organs, 2003, 6 (4) :236-244