Differentiation of a hepatic phenotype after heterotropic transplantation of heart, kidney, brain, and skin tissues into liver in F344 rats

Biochemical and Biophysical Research Communications Volume 354 Issue 4 Page 841-845 published_at 2007-03-23
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Title ( eng )
Differentiation of a hepatic phenotype after heterotropic transplantation of heart, kidney, brain, and skin tissues into liver in F344 rats
Creator
Ochiya Takahiro
Ueda Shinobu
Kominami Yoko
Gon Rina
Nishiki Masayo
Hayashi Masaomi
Sasaki Atsushi
Shiraishi Miho
Kashimoto Naoki
Myojin Yuki
Source Title
Biochemical and Biophysical Research Communications
Volume 354
Issue 4
Start Page 841
End Page 845
Abstract
While organ-specific stem cells with roles in tissue injury repair have been documented, their pathogenic significance in diseases and the factors potentially responsible for their activation remain largely unclear. In the present study, heart, kidney, brain, and skin samples from F344 transgenic rats carrying the GFP gene were transplanted into normal F344 rat liver one day after an intraperitoneal injection (i.p.) of carbon tetrachloride (CCl4) to test their differentiation capacity. The transplantation was carried out by female donors to male recipients, and vice versa. One week after transplantation, GFP antigen-positive cells with phenotypic characteristics of hepatocytes were noted. After two weeks, their extent increased, and at 4 weeks, large areas of strongly GFP-stained cells developed. All recipient livers had GFP antigen-positive hepatocyte cells. PCR analysis coupled with laser capture micro-dissection (LCM) revealed those cells to contain GFP DNA. Thus, our results indicate that tissue stem cells have multipotential ability, differentiating into hepatocytes when transplanted into an injured liver.
Keywords
Differentiation
Hepatocyte
Transplantation
Stem cells
Liver
GFP
Transgenic rat
CCl4
NDC
Medical sciences [ 490 ]
Language
eng
Resource Type journal article
Publisher
Elsevier
Date of Issued 2007-03-23
Rights
Copyright (c) 2007 Elsevier Inc. All rights reserved.
Publish Type Author’s Original
Access Rights open access
Source Identifier
[ISSN] 0006-291X
[DOI] 10.1016/j.bbrc.2006.12.236
[NCID] AA00564395
[DOI] http://dx.doi.org/10.1016/j.bbrc.2006.12.236