Microfibrillated Cellulose Sheets Coating Oxygen-Permeable PDMS Membranes Induce Rat Hepatocytes 3D Aggregation into Stably-Attached 3D Hemispheroids

被引:20
作者
Evenou, Fanny [1 ]
Couderc, Sandrine [1 ]
Kim, Beomjoon [2 ]
Fujii, Teruo [2 ]
Sakai, Yasuyuki [2 ]
机构
[1] Univ Tokyo, Inst Ind Sci, Lab Integrated Micromech Syst LIMMS CNRS IIS, Meguro Ku, Tokyo 1538505, Japan
[2] Univ Tokyo, Inst Ind Sci IIS, Meguro Ku, Tokyo 1538505, Japan
关键词
Hepatocyte; 3D culture; multicellular aggregate; cellulose; oxygen; PDMS membrane; liver function; POLYMERIC MEMBRANES; MELANOMA-CELLS; LIVER; CULTURE; MAINTENANCE; SUBSTRATUM; SPHEROIDS; SURFACE; FIBROBLASTS; CONSUMPTION;
D O I
10.1163/092050610X513242
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Here we report the use of natural, chemically-unmodified, microfibrillated cellulose (MFC) as a matrix for hepatocyte culture. We developed an original cell-culture design composed of a thin 3D-microstructured fibrous substrate consisting of a MFC sheet coating a highly O-2-permeable polydimethylsiloxane (PDMS) membrane. The MFC-coated PDMS membranes were obtained according to a simple process where cellulose fibres were deposited from an aqueous suspension on the PDMS surfaces and the films were dried under mild conditions. To enable oxygen diffusion through the membranes, they were assembled on bottomless frames ('O-2+' condition). Rat hepatocytes primary-cultured on such MFC-PDMS membranes quickly organized themselves into large hemispherical 3D aggregates which were tightly anchored to the MFC sheets. In contrast, hepatocytes cultured on smooth PDMS membranes in the O-2+ system (O-2+, PDMS) organized into unstable 2D monolayers which easily detached from the surfaces. Hepatocyte 3D cultures obtained on MFC-PDMS membranes exhibited higher liver-specific functions over a 2-week culture period, as assessed by both the higher albumin secretion and urea synthesis rate. The MFC-PDMS membranes appear suitable for obtaining stably-attached and functional hepatocyte 3D cultures and appear interesting for drug/chemical screenings in a microplate format, but also for microfluidic applications. (C) Koninklijke Brill NV, Leiden, 2011
引用
收藏
页码:1509 / 1522
页数:14
相关论文
共 40 条
[1]
Modification of nanocellulose with a xyloglucan-RGD conjugate enhances adhesion and proliferation of endothelial cells: Implications for tissue engineering [J].
Bodin, Aase ;
Ahrenstedt, Lage ;
Fink, Helen ;
Brumer, Harry ;
Risberg, Bo ;
Gatenholm, Paul .
BIOMACROMOLECULES, 2007, 8 (12) :3697-3704
[2]
Induction of zone-like liver function gradients in HepG2 cells by varying culture medium height [J].
Camp, James P. ;
Capitano, Adam T. .
BIOTECHNOLOGY PROGRESS, 2007, 23 (06) :1485-1491
[3]
Polymeric membranes for hybrid liver support devices: The effect of membrane surface wettability on hepatocyte viability and functions [J].
Catapano, G ;
DiLorenzo, MC ;
DellaVolpe, C ;
DeBartolo, L ;
Migliaresi, C .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 1996, 7 (11) :1017-1027
[4]
Diffusion of gases in silicone polymers: Molecular dynamics simulations [J].
Charati, SG ;
Stern, SA .
MACROMOLECULES, 1998, 31 (16) :5529-5535
[5]
DEPENDENCE OF LIVER-SPECIFIC TRANSCRIPTION ON TISSUE ORGANIZATION [J].
CLAYTON, DF ;
HARRELSON, AL ;
DARNELL, JE .
MOLECULAR AND CELLULAR BIOLOGY, 1985, 5 (10) :2623-2632
[6]
The effect of surface roughness of microporous membranes on the kinetics of oxygen consumption and ammonia elimination by adherent hepatocytes [J].
De Bartolo, L ;
Catapano, G ;
Della Volpe, C ;
Drioli, E .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 1999, 10 (06) :641-655
[7]
Evaluation of cell behaviour related to physico-chemical properties of polymeric membranes to be used in bioartificial organs [J].
De Bartolo, L ;
Morelli, S ;
Bader, A ;
Drioli, E .
BIOMATERIALS, 2002, 23 (12) :2485-2497
[8]
Evaluation of the biodegradation of starch and cellulose under controlled composting conditions [J].
Degli-Innocenti, F ;
Tosin, M ;
Bastioli, C .
JOURNAL OF ENVIRONMENTAL POLYMER DEGRADATION, 1998, 6 (04) :197-202
[9]
Ultrastructural and functional investigations of adult hepatocyte spheroids during in vitro cultivation [J].
Dvir-Ginzberg, M ;
Elkayam, T ;
Aflalo, ED ;
Agbaria, R ;
Cohen, S .
TISSUE ENGINEERING, 2004, 10 (11-12) :1806-1817
[10]
Enzymatic degradation of model cellulose films [J].
Eriksson, J ;
Malmsten, M ;
Tiberg, F ;
Callisen, TH ;
Damhus, T ;
Johansen, KS .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2005, 284 (01) :99-106