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Fas‐mediated apoptosis is involved in the elimination of gene‐transduced hepatocytes with E1/E3‐deleted adenoviral vectors
Author(s) -
OKUYAMA TORAYUKI,
LI XIAO-KANG,
FUNESHIMA NAOKO,
FUJINO MASAYUKI,
SASAKI KYOKO,
KITA YUSUKE,
KOSUGA MOTOMICHI,
TAKAHASHI MASAHIKO,
SAITO HIDETSUGU,
SUZUKI SEIICHI,
YAMADA MASAO
Publication year - 1998
Publication title -
journal of gastroenterology and hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.214
H-Index - 130
eISSN - 1440-1746
pISSN - 0815-9319
DOI - 10.1111/jgh.1998.13.s1.113
Subject(s) - apoptosis , tunel assay , microbiology and biotechnology , viral vector , transduction (biophysics) , lac operon , fas ligand , biology , hepatocyte , adenoviridae , transgene , genetic enhancement , reporter gene , programmed cell death , gene , gene expression , recombinant dna , biochemistry , in vitro
Gene‐transduced hepatocytes with E1/E3‐deleted adenoviral vectors are eliminated immediately and the expression of transduced genes disappears rapidly following the vector administration. In this report, we analysed the involvement of apoptotic cell death in the elimination of hepatocytes infected with adenoviral vectors. An E1/E3‐deleted adenoviral vector expressing Escherichia coli β‐galactosidase (LacZ) was injected via the portal vein into congenitally Fas‐deficient mice (lpr), Fas ligand‐deficient mice (gld) and their control mice, MRL and C3H. 5‐Bromo‐4‐chloro‐3‐indolyl‐β‐D‐galactoside (X‐gal) staining of the liver specimens showed that 80–100% of hepatocytes were LacZ positive at 7 days after virus administration, suggesting that most of the hepatocytes received the injected adenoviral vectors. In normal mice, the number of LacZ‐positive cells decreased dramatically at 14 and 21 days after transduction and few positive cells were observed at day 28. β‐Galactosidase activity, quantified by the O‐nitrophenyl‐beta‐D‐galactopyranoside assay, gave comparable results to X‐gal staining. At days 14 or 21, many apoptotic hepatocytes and apoptotic infiltrating cells were detected with the terminal deoxyribonucleotidyl transferase‐mediated dUTP‐digoxigenin nick end‐labelling (TUNEL) in situ apoptosis detection method. This observation suggested that the apoptotic process was associated with the elimination of adenovirus‐infected hepatocytes. To test the involvement of the Fas—Fas ligand interaction in this apoptotic process, the period of transgene expression was measured in 1pr and gld mice, which had received the same amount of AxCALacZ. X‐Gal histochemical analysis detected many LacZ‐positive cells in 1pr or gld mice liver even at 21 or 28 days after AxCALacZ injection. There were significant differences in the reduction rates of β‐galactosidase activity of liver homogenates between lpr and MRL, or gld and C3H mice. Based on these observations, we conclude that the Fas‐mediated apoptotic process is involved in the elimination of hepatocytes infected with E1/E3‐deleted adenoviral vectors.