Originally published as JHC exPRESS on September 28, 2009. doi:10.1369/jhc.2009.954560 Journal of Histochemistry and Cytochemistry Volume 58 (1): 61-72, 2010 Copyright © 2010 Tateno et al.
Endogenous and Transplanted Small Hepatocytes in Retrorsine-treated/Partially Hepatectomized Rat Liver Show Differences in Growth, Phenotype, and Proximity to Clusters of
Department of Medicine, Division of Hematology and Oncology, Rhode Island Hospital and Brown University Medical School, Providence, Rhode Island (MPC,DCH), and Hiroshima Tissue Regeneration Project, Hiroshima Prefectural Institute of Science and Technology, Hiroshima, Japan (CT) Correspondence to: Dr. Douglas C. Hixson, PhD, Director, COBRE CCRD, Rhode Island Hospital, 593 Eddy Street, Providence, RI 02903. E-mail: douglas_hixson{at}brown.edu
In the present report, we have compared the phenotype and growth of small hepatocyte progenitors (SHPs) induced by retrorsine/partial hepatectomy (R/PH) and small hepatocytes (SHs) isolated from normal adult liver. SHs were isolated by a combination of differential centrifugation and Percoll isodensity fractionation from a liver cell suspension prepared by collagenase perfusion of a dipeptidyl peptidase IV (DPPIV)–positive Fischer F344 rat liver. Following further purification by flow cytometry, the SH-R3 fraction was transplanted via the portal vein into R/PH–treated, DPPIV-negative Fischer F344 rats. Frozen sections from tissue harvested at 5, 7, and 21 days after transplantation were analyzed by indirect immunofluorescence to compare the phenotypic characteristics of colonies formed by exogenous SH-R3s and endogenous SHPs. Colonies of transplanted SHs and endogenous SHPs displayed similar histologies and phenotypes but were distinguished from surrounding hepatocytes by their elevated expression of transferrin receptor. SH-R3 colonies were frequently located within clusters of
Key Words: small hepatocyte monoclonal antibody retrorsine partial hepatectomy transplantation bipotent phenotype rat transferrin receptor dipeptidyl peptidase IV
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