| Literature DB >> 28448819 |
Kazuki Sasaki1, Takami Akagi2, Tadafumi Asaoka1, Hidetoshi Eguchi1, Yasunari Fukuda1, Yoshifumi Iwagami1, Daisaku Yamada1, Takehiro Noda1, Hiroshi Wada1, Kunihito Gotoh1, Koichi Kawamoto1, Yuichiro Doki1, Masaki Mori1, Mitsuru Akashi3.
Abstract
The creation of artificial liver tissue is an active area of research due to the shortage of donors for liver transplantation. Here we investigated whether a simple and efficient cell coating technique developed in our laboratory could be used to generate functional vascularized liver tissue. This technique creates three-dimensional tissue by loading cells sterically onto other cells that have been coated with layer-by-layer (LbL) nanofilms of fibronectin and gelatin, two extracellular matrix proteins. We used this technique to construct homogenous, dense, well-vascularized liver tissue from cryopreserved human primary hepatocytes, human umbilical vein endothelial cells, and normal human dermal fibroblasts. Using LbL cell coating technique resulted in higher cellular function in terms of human albumin production (P < 0.01) and cytochrome P450 activity (P < 0.01) in vitro. Furthermore, after being transplanted subcutaneously into NOD/SCID mice, the vascularized liver tissue showed greater albumin production in the early stage than non-vascularized tissue or a hepatocyte suspension (P < 0.01). Histological examination demonstrated that compare to non-vascularized tissue, there were many less-morphologically changed and intact hepatocytes in the vascularized tissue. This cell coating technique would be applicable to the generation of vascularized functional liver tissue for regenerative medicine in the future.Entities:
Keywords: Cell coating technique; Cryopreserved human primary hepatocytes; Layer-by-layer; Vascularized liver tissue
Mesh:
Year: 2017 PMID: 28448819 DOI: 10.1016/j.biomaterials.2017.02.034
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479