TY - JOUR
T1 - IL-1β and TNF-α suppress apolipoprotein (APO) E secretion and APO A-I expression in HepG2 cells
AU - Song, Hua
AU - Saito, Kuniaki
AU - Fujigaki, Suwako
AU - Noma, Akio
AU - Ishiguro, Hiroshi
AU - Nagatsu, Toshiharu
AU - Seishima, Mitsuru
N1 - Funding Information:
We would like to thank the Japanese Cancer Research Resources Bank for their generous gift of apo E cDNA probes[ We also appreciate Mochida Pharmaceutical Co[ for a gift of IFN!b\ Kyowa Medex Co[ for Determiner!TC and Daiichi Pure Chemical Co[ for antibodies to apo A!I and apo E[ This work was supported in part by a Grant!in!Aid for Scienti_c Research No[ 96661143 from the Japanese Ministry of Education\ Science and Culture[
PY - 1998/4
Y1 - 1998/4
N2 - The effect of cytokines on apolipoprotein E (ape E) production and secretion was investigated in a human hepatoma cell line HepG2. Incubation of HepG2 cells with interleukin 1β (IL-1β) or tumour necrosis factor α (TNF-α) for 48 h resulted in a significant dose-related decrease of apo E concentration in the culture medium, while intracellular apo E content increased without change in mRNA level. In contrast, IL-1β and TNF-α decreased both intracellular and medium apo A-I. Elution profiles of cholesterol and apolipoproteins revealed that apo E was present in apo E-rich high density lipoprotein (HDL) fraction and apo A-I was in apo E-rich HDL and small HDL fractions. IL-1β and TNF-α decreased both apo E and apo A-I in these fractions. The present results suggest that IL-1β and TNF-α suppress hepatic apo A-I expression and secretion but not expression of apo E, which could contribute to the abnormal lipid metabolism in certain cytokine-mediated inflammatory diseases.
AB - The effect of cytokines on apolipoprotein E (ape E) production and secretion was investigated in a human hepatoma cell line HepG2. Incubation of HepG2 cells with interleukin 1β (IL-1β) or tumour necrosis factor α (TNF-α) for 48 h resulted in a significant dose-related decrease of apo E concentration in the culture medium, while intracellular apo E content increased without change in mRNA level. In contrast, IL-1β and TNF-α decreased both intracellular and medium apo A-I. Elution profiles of cholesterol and apolipoproteins revealed that apo E was present in apo E-rich high density lipoprotein (HDL) fraction and apo A-I was in apo E-rich HDL and small HDL fractions. IL-1β and TNF-α decreased both apo E and apo A-I in these fractions. The present results suggest that IL-1β and TNF-α suppress hepatic apo A-I expression and secretion but not expression of apo E, which could contribute to the abnormal lipid metabolism in certain cytokine-mediated inflammatory diseases.
UR - https://www.scopus.com/pages/publications/0032055838
UR - https://www.scopus.com/pages/publications/0032055838#tab=citedBy
U2 - 10.1006/cyto.1997.0291
DO - 10.1006/cyto.1997.0291
M3 - Article
C2 - 9617572
AN - SCOPUS:0032055838
SN - 1043-4666
VL - 10
SP - 275
EP - 280
JO - Cytokine
JF - Cytokine
IS - 4
ER -