Technique for the control of spheroid diameter using microfabricated chips

被引:83
作者
Sakai, Yusuke [1 ]
Nakazawa, Kohji [1 ]
机构
[1] Univ Kitakyushu, Dept Chem Proc & Environm, Fukuoka 8080135, Japan
关键词
HepG2; spheroid; microfabrication; polyethylene glycol; liver functions;
D O I
10.1016/j.actbio.2007.06.004
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
This paper describes a new technique for the control of spheroid diameter in.,liver-derived cell lines using microfabricated chips that were prepared by combining microfabrication with chemical surface modification. The chip possesses multicavities in a triangular arrangement in the central region (10 mm x 10 mm) of a polymethylinethacrylate (PMMA) plate (24 mm x 24 mm), and the surface of the chip was modified with polyethylene glycol, thereby producing a surface that is non-adhesive to cells. HepG2 cells, a model liver-derived cell line, inoculated onto the chip were trapped-within each cavity and proliferated to gradually form spheroids with smooth surfaces and high circularity. Although the spheroid diameters increased with cell proliferation during the initial 10 days of culture, they remained constant thereafter. The spheroid diameters were dependent on the scales of the multicavities on the chip, and the spheroid configuration with uniform diameter was maintained for at least I month. In particular, it was demonstrated using chips of various designs that the cavity diameter and the pitch between cavities were effective factors in controlling the spheroid diameter. Furthermore, the protein secretion activities of the spheroid formed on the chip were higher than those of the monolayers for at least 1 month of culture. These results indicate that this chip is a useful technique for the control of spheroid diameter and for the mass preparation of uniform spheroids. (C) 2007 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1033 / 1040
页数:8
相关论文
共 31 条
[1]   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
[2]   Hepatocyte polarity and the peroxisomal compartment: a comparative study [J].
Depreter, M ;
Walker, T ;
De Smet, K ;
Beken, S ;
Kerckaert, I ;
Rogiers, V ;
Roels, F .
HISTOCHEMICAL JOURNAL, 2002, 34 (3-4) :139-151
[3]   Novel hepatocyte culture system developed using microfabrication and collagen/polyethylene glycol microcontact printing [J].
Fukuda, J ;
Sakai, Y ;
Nakazawa, K .
BIOMATERIALS, 2006, 27 (07) :1061-1070
[4]   Orderly arrangement of hepatocyte spheroids on a microfabricated chip [J].
Fukuda, J ;
Nakazawa, K .
TISSUE ENGINEERING, 2005, 11 (7-8) :1254-1262
[5]   Efficacy of a polyurethane foam/spheroid artificial liver by using human hepatoblastoma cell line (Hep G2) [J].
Fukuda, J ;
Okamura, K ;
Nakazawa, K ;
Ijima, H ;
Yamashita, Y ;
Shimada, M ;
Shirabe, K ;
Tsujita, E ;
Sugimachi, K ;
Funatsu, K .
CELL TRANSPLANTATION, 2003, 12 (01) :51-58
[6]   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
[7]   The use of genomics technology to investigate gene expression changes in cultured human liver cells [J].
Harries, HM ;
Fletcher, ST ;
Duggan, CM ;
Baker, VA .
TOXICOLOGY IN VITRO, 2001, 15 (4-5) :399-405
[8]   Hepatocyte spheroids in polyurethane foams: Functional analysis and application for a hybrid artificial liver [J].
Ijima, H ;
Matsushita, T ;
Nakazawa, K ;
Fujii, Y ;
Funatsu, K .
TISSUE ENGINEERING, 1998, 4 (02) :213-226
[9]   Method for generation of homogeneous multicellular tumor spheroids applicable to a wide variety of cell types [J].
Kelm, JM ;
Timmins, NE ;
Brown, CJ ;
Fussenegger, M ;
Nielsen, LK .
BIOTECHNOLOGY AND BIOENGINEERING, 2003, 83 (02) :173-180
[10]   Human hepatocyte cell lines proliferating as cohesive spheroid colonies in alginate markedly upregulate both synthetic and detoxificatory liver function [J].
Khalil, M ;
Shariat-Panahi, A ;
Tootle, R ;
Ryder, T ;
McCloskey, P ;
Roberts, E ;
Hodgson, H ;
Selden, C .
JOURNAL OF HEPATOLOGY, 2001, 34 (01) :68-77