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Originally published In Press as doi:10.1074/jbc.M106888200 on September 27, 2001

J. Biol. Chem., Vol. 276, Issue 48, 44512-44520, November 30, 2001
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Apolipoprotein A-V
A NOVEL APOLIPOPROTEIN ASSOCIATED WITH AN EARLY PHASE OF LIVER REGENERATION*

Hendrik N. van der VlietDagger , Martijn Groenink SammelsDagger , Aad C. J. Leegwater§, Johannes H. M. Levels§, Pieter H. Reitsma§, Willem BoersDagger , and Robert A. F. M. ChamuleauDagger

From the Departments of Dagger  Experimental Hepatology and § Experimental Internal Medicine, Academic Medical Center, University of Amsterdam, Meibergdreef 9, Amsterdam 1105 AZ, The Netherlands

Liver regeneration in response to various forms of liver injury is a complex process, which ultimately results in restoration of the original liver mass and function. Because the underlying mechanisms that initiate this response are still incompletely defined, this study was aimed to identify novel factors. Liver genes that were up-regulated 6 h after 70% hepatectomy (PHx) in the rat were selected by cDNA subtractive hybridization. Besides known genes associated with cell proliferation, several novel genes were isolated. The novel gene that was most up-regulated was further studied. Its mRNA showed a liver-specific expression and encoded a protein comprising 367 amino acids. The mouse and human cDNA analogues were also isolated and appeared to be highly homologous. The human gene analogue was located at an apolipoprotein gene cluster on chromosome 11q23. The protein encoded by this gene had appreciable homology with apolipoproteins A-I and A-IV. Maximal expression of the gene in the rat liver and its gene product in rat plasma was observed 6 h after PHx. The protein was present in plasma fractions containing high density lipoprotein particles. Therefore, we have identified a novel apolipoprotein, designated apolipoprotein A-V, that is associated with an early phase of liver regeneration.


* The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EMBL Data Bank with accession number(s) AF202887, AF202888, AF327059, AF202889, and AF202890.

To whom correspondence should be addressed: Dept. of Gastroenterology and Hepatology, Room C2-331, Academic Medical Center, University of Amsterdam, P.O. Box 22660, Amsterdam 1100 DD, The Netherlands. Tel.: 31-20-566-2422; Fax: 31-20-691-7033; E-mail: r.a. chamuleau@amc.uva.nl.


Copyright © 2001 by The American Society for Biochemistry and Molecular Biology, Inc.
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