3D liver models on a microplatform: well-defined culture, engineering of liver tissue and liver-on-a-chip

被引:142
作者
No, Da Yoon [1 ,4 ]
Lee, Kwang-Ho [2 ]
Lee, Jaeseo [1 ,3 ]
Lee, Sang-Hoon [1 ,3 ]
机构
[1] Korea Univ, Coll Hlth Sci, Dept Biomed Engn, Seoul 136701, South Korea
[2] Kangwon Natl Univ, Coll Engn, Dept Adv Mat Sci & Engn, Chunchon 200701, South Korea
[3] Korea Univ, KU KIST Grad Sch Converging Sci & Technol, Seoul 136703, South Korea
[4] Stanford Univ, Sch Engn & Med, Dept Bioengn, Stanford, CA 94305 USA
基金
新加坡国家研究基金会;
关键词
CELL MICROENCAPSULATION TECHNOLOGY; GROWTH-FACTOR DELIVERY; FUNCTIONAL HUMAN LIVER; IN-VITRO; LONG-TERM; PRIMARY HEPATOCYTES; RAT HEPATOCYTES; 3-DIMENSIONAL CULTURE; PORCINE HEPATOCYTES; PANCREATIC-ISLETS;
D O I
10.1039/c5lc00611b
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The liver, the largest organ in the human body, is a multi-functional organ with diverse metabolic activities that plays a critical role in maintaining the body and sustaining life. Although the liver has excellent regenerative and recuperative properties, damages caused by chronic liver diseases or viral infection may lead to permanent loss of liver functions. Studies of liver disease mechanism have focused on drug screening and liver tissue engineering techniques, including strategies based on in vitro models. However, conventional liver models are plagued by a number of limitations, which have motivated the development of 'liver-on-a-chip' and microplatform-based bioreactors that can provide well-defined microenvironments. Microtechnology is a promising tool for liver tissue engineering and liver system development, as it can mimic the complex in vivo microenvironment and microlevel ultrastructure, by using a small number of human cells under two-dimensional (2D) and three-dimensional (3D) culture conditions. These systems provided by microtechnology allow improved liver-specific functions and can be expanded to encompass diverse 3D culture methods, which are critical for the maintenance of liver functions and recapitulation of the features of the native liver. In this review, we provide an overview of microtechnologies that have been used for liver studies, describe biomimetic technologies for constructing microscale 2D and 3D liver models as well as liver-on-a-chip systems and microscale bioreactors, and introduce applications of liver microtechnology and future trends in the field.
引用
收藏
页码:3822 / 3837
页数:16
相关论文
共 150 条
[81]   Human-on-chip for therapy development and fundamental science [J].
Luni, Camilla ;
Serena, Elena ;
Elvassore, Nicola .
CURRENT OPINION IN BIOTECHNOLOGY, 2014, 25 :45-50
[82]   Characterization of a Gastrointestinal Tract Microscale Cell Culture Analog Used to Predict Drug Toxicity [J].
Mahler, Gretchen J. ;
Esch, Mandy B. ;
Glahn, Raymond P. ;
Shuler, Michael L. .
BIOTECHNOLOGY AND BIOENGINEERING, 2009, 104 (01) :193-205
[83]   A four-organ-chip for interconnected long-term co-culture of human intestine, liver, skin and kidney equivalents [J].
Maschmeyer, Ilka ;
Lorenz, Alexandra K. ;
Schimek, Katharina ;
Hasenberg, Tobias ;
Ramme, Anja P. ;
Huebner, Juliane ;
Lindner, Marcus ;
Drewell, Christopher ;
Bauer, Sophie ;
Thomas, Alexander ;
Sambo, Naomia Sisoli ;
Sonntag, Frank ;
Lauster, Roland ;
Marx, Uwe .
LAB ON A CHIP, 2015, 15 (12) :2688-2699
[84]   Improved Survival of Fulminant Liver Failure by Transplantation of Microencapsulated Cryopreserved Porcine Hepatocytes in Mice [J].
Mei, Jie ;
Sgroi, Antonino ;
Mai, Gang ;
Baertschiger, Reto ;
Gonelle-Gispert, Carmen ;
Serre-Beinier, Veronique ;
Morel, Philippe ;
Buehler, Leo H. .
CELL TRANSPLANTATION, 2009, 18 (01) :101-110
[85]   Multi-cell type human liver microtissues for hepatotoxicity testing [J].
Messner, S. ;
Agarkova, I. ;
Moritz, W. ;
Kelm, J. M. .
ARCHIVES OF TOXICOLOGY, 2013, 87 (01) :209-213
[86]   Cell microencapsulation technology: Towards clinical application [J].
Murua, Ainhoa ;
Portero, Aitziber ;
Orive, Gorka ;
Hernandez, Rosa M. ;
de Castro, Maria ;
Luis Pedraz, Jose .
JOURNAL OF CONTROLLED RELEASE, 2008, 132 (02) :76-83
[87]   Immune-protected xenogeneic bioartificial livers with liver-specific microarchitecture and hydrogel-encapsulated cells [J].
No, Da Yoon ;
Jeong, Gi Seok ;
Lee, Sang-Hoon .
BIOMATERIALS, 2014, 35 (32) :8983-8991
[88]   A microfluidic hepatic coculture platform for cell-based drug metabolism studies [J].
Novik, Eric ;
Maguire, Timothy J. ;
Chao, Piyun ;
Cheng, K. C. ;
Yarmush, Martin L. .
BIOCHEMICAL PHARMACOLOGY, 2010, 79 (07) :1036-1044
[89]   Three-dimensional culture and cAMP signaling promote the maturation of human pluripotent stem cell-derived hepatocytes [J].
Ogawa, Shinichiro ;
Surapisitchat, James ;
Virtanen, Carl ;
Ogawa, Mina ;
Niapour, Maryam ;
Sugamori, Kim S. ;
Wang, Shuang ;
Tamblyn, Laura ;
Guillemette, Chantal ;
Hoffmann, Ewa ;
Zhao, Bin ;
Strom, Stephen ;
Laposa, Rebecca R. ;
Tyndale, Rachel F. ;
Grant, Denis M. ;
Keller, Gordon .
DEVELOPMENT, 2013, 140 (15) :3285-3296
[90]   Engineering functional two- and three-dimensional liver systems in vivo using hepatic tissue sheets [J].
Ohashi, Kazuo ;
Yokoyama, Takashi ;
Yamato, Masayuki ;
Kuge, Hiroyuki ;
Kanehiro, Hiromichi ;
Tsutsumi, Masahiro ;
Amanuma, Toshihiro ;
Iwata, Hiroo ;
Yang, Joseph ;
Okano, Teruo ;
Nakajima, Yoshiyuki .
NATURE MEDICINE, 2007, 13 (07) :880-885