Engineering functional two- and three-dimensional liver systems in vivo using hepatic tissue sheets

Author:  ["Kazuo Ohashi","Takashi Yokoyama","Masayuki Yamato","Hiroyuki Kuge","Hiromichi Kanehiro","Masahiro Tsutsumi","Toshihiro Amanuma","Hiroo Iwata","Joseph Yang","Teruo Okano","Yoshiyuki Nakajima"]

Publication:  Nature Medicine

CITE.CC academic search helps you expand the influence of your papers.

Tags:     Medicine

Abstract

Hepatic tissue engineering using primary hepatocytes has been considered a valuable new therapeutic modality for several classes of liver diseases. Recent progress in the development of clinically feasible liver tissue engineering approaches, however, has been hampered mainly by insufficient cell-to-cell contact of the engrafted hepatocytes. We developed a method to engineer a uniformly continuous sheet of hepatic tissue using isolated primary hepatocytes cultured on temperature-responsive surfaces. Sheets of hepatic tissue transplanted into the subcutaneous space resulted in efficient engraftment to the surrounding cells, with the formation of two-dimensional hepatic tissues that stably persisted for longer than 200 d. The engineered hepatic tissues also showed several characteristics of liver-specific functionality. Additionally, when the hepatic tissue sheets were layered in vivo, three-dimensional miniature liver systems having persistent survivability could be also engineered. This technology for liver tissue engineering is simple, minimally invasive and free of potentially immunogenic biodegradable scaffolds.

Cite this article

Ohashi, K., Yokoyama, T., Yamato, M. et al. Engineering functional two- and three-dimensional liver systems in vivo using hepatic tissue sheets. Nat Med 13, 880–885 (2007). https://doi.org/10.1038/nm1576

View full text

>> Full Text:   Engineering functional two- and three-dimensional liver systems in vivo using hepatic tissue sheets

Inhibition of CDK1 as a potential therapy for tumors over-expressing MYC

Identification of a key pathway required for the sterile inflammatory response triggered by dying ce