LPS and cytokines regulate extra hepatic mRNA levels of apolipoproteins during the acute phase response in Syrian hamsters

被引:45
作者
Hardardottir, I
Sipe, J
Moser, AH
Fielding, CJ
Feingold, KR
Grunfeld, C
机构
[1] UNIV CALIF SAN FRANCISCO,DEPT MED,SAN FRANCISCO,CA 94143
[2] DEPT VET AFFAIRS MED CTR,MED SERV,METAB SECT,SAN FRANCISCO,CA 94121
[3] BOSTON UNIV,SCH MED,DEPT BIOCHEM,BOSTON,MA 02118
[4] UNIV CALIF SAN FRANCISCO,MED CTR,CARDIOVASC RES INST,SAN FRANCISCO,CA 94143
来源
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM | 1997年 / 1344卷 / 03期
关键词
apolipoprotein; acute phase response; endotoxin; cytokine; (Syrian hamster);
D O I
10.1016/S0005-2760(96)00143-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Altered hepatic expression of apolipoproteins occurs during the acute phase response. Here we examined whether the acute phase response alters extra hepatic expression of apolipoproteins. Syrian hamsters were injected with endotoxin (LPS), tumor necrosis factor (TNF), interleukin (IL)-1, or the combination of TNF + IL-1 and mRNAs for serum amyloid A (apoSAA), apolipoprotein (apo) J, apo E, apo A-I, and apo D, were analyzed. LPS increased mRNA levels for apoSAA in all tissues examined. LPS and TNF + IL-1 increased mRNA levels for apo J in kidney, heart, stomach, intestine, and muscle. Individually, TNF and IL-1 were less potent than the combination of the two cytokines. LPS decreased mRNA levels for apo E in all tissues, except for mid and distal intestine. TNF and IL-1 were less effective than LPS. LPS, TNF + IL-1 and TNF decreased mRNA levels for apo A-I in duodenum. mRNA for apo D decreased in heart, were unchanged in brain and increased in muscle, following LPS. The widespread extra hepatic regulation of the apolipoproteins during the acute phase response may be important for the alterations in lipid metabolism that occur during infection and inflammation as well as the immune response.
引用
收藏
页码:210 / 220
页数:11
相关论文
共 72 条
[1]   COMPLEMENTARY-DNA SEQUENCING - EXPRESSED SEQUENCE TAGS AND HUMAN GENOME PROJECT [J].
ADAMS, MD ;
KELLEY, JM ;
GOCAYNE, JD ;
DUBNICK, M ;
POLYMEROPOULOS, MH ;
XIAO, H ;
MERRIL, CR ;
WU, A ;
OLDE, B ;
MORENO, RF ;
KERLAVAGE, AR ;
MCCOMBIE, WR ;
VENTER, JC .
SCIENCE, 1991, 252 (5013) :1651-1656
[2]  
ARBEENY CM, 1992, J LIPID RES, V33, P843
[3]   APOLIPOPROTEIN-J EXPRESSION AT FLUID-TISSUE INTERFACES - POTENTIAL ROLE IN BARRIER CYTOPROTECTION [J].
ARONOW, BJ ;
LUND, SD ;
BROWN, TL ;
HARMONY, JAK ;
WITTE, DP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (02) :725-729
[4]   SERUM AMYLOID-A IS A CHEMOATTRACTANT - INDUCTION OF MIGRATION, ADHESION, AND TISSUE INFILTRATION OF MONOCYTES AND POLYMORPHONUCLEAR LEUKOCYTES [J].
BADOLATO, R ;
WANG, JM ;
MURPHY, WJ ;
LLOYD, AR ;
MICHIEL, DF ;
BAUSSERMAN, LL ;
KELVIN, DJ ;
OPPENHEIM, JJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (01) :203-209
[5]  
BANKA CL, 1995, J LIPID RES, V36, P1058
[6]   SYNTHESIS AND REGULATION OF ACUTE PHASE PLASMA-PROTEINS IN PRIMARY CULTURES OF MOUSE HEPATOCYTES [J].
BAUMANN, H ;
JAHREIS, GP ;
GAINES, KC .
JOURNAL OF CELL BIOLOGY, 1983, 97 (03) :866-876
[7]  
BOYLES JK, 1990, J LIPID RES, V31, P2243
[8]  
CABANA VG, 1989, J LIPID RES, V30, P39
[9]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[10]  
COLTEN HR, 1992, J APPL PHYSIOL, V72, P1