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Hepatocyte proliferation factors from neonatal pig liver: Purification and characterization
Author(s) -
Hiyoshi Mineyoshi,
Ohkubo Tomoichi,
Tsuji Kimiyoshi,
Hagihara Masao,
Nakasaki Hisao,
Mukai Masaya,
Makuuchi Hiroyasu,
Yamamura Masaichi,
Tsuda Michio
Publication year - 2002
Publication title -
biofactors
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.204
H-Index - 94
eISSN - 1872-8081
pISSN - 0951-6433
DOI - 10.1002/biof.5520160101
Subject(s) - hepatocyte , size exclusion chromatography , sepharose , chemistry , microbiology and biotechnology , molecular mass , dna , chromatography , dna synthesis , elution , biochemistry , biology , in vitro , enzyme
Two factors were found in the condition medium of neonatal pig liver fragments, which were capable of stimulating DNA synthesis in primary hepatocytes. They were named hepatocyte proliferation factor (HPF)‐1 and HPF‐2 and purified 1,025‐ and 2,580‐fold, respectively. Both HPF‐1 and HPF‐2 seem to be anionic at pH 8.0 judged from the elution pattern of DEAE (DE52) column chromatography. HPF‐1 was recovered as a non‐adsorbed fraction in blue Sepharose and heparin Sepharose columns, and had a molecular weight of 26–31 kDa as estimated by gel filtration in high salt condition. Purified HPF‐1 stimulated DNA synthesis of primary rat hepatocytes, but suppressed that of HepG2 cells. HPF‐2 strongly bound to blue Sepharose and heparin Sepharose columns, and had a molecular weight of 71–90 kDa as estimated by SDS‐PAGE under non‐reduced condition. Purified HPF‐2 stimulated DNA synthesis of primary rat hepatocytes dose dependently but did not suppress that of HepG2 cells. From further biological and chemical characteristics studied in this paper, HPF‐1 and HPF‐2 may be novel stimulating proteins for hepatocyte proliferation, although the possibility that they are already known growth factors can not be excluded without complete purification and its cloning.