The Influence of Estrogen on Hepatobiliary Osteopontin (SPP1) Expression in a Female Rodent Model of Alcoholic Steatohepatitis

被引:12
作者
Banerjee, Atrayee [1 ]
Rose, Robert [1 ]
Johnson, Greg A.
Burghardt, Robert C.
Ramaiah, Shashi K. [1 ]
机构
[1] Texas A&M Univ, Coll Vet Med & Biomed Sci, Dept Pathobiol, College Stn, TX 77843 USA
关键词
alcoholic steatohepatitis; estrogen; liver; inflammation; osteopontin; SECRETED PHOSPHOPROTEIN-1 OSTEOPONTIN; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; INDUCED LIVER-INJURY; NF-KAPPA-B; GENE-EXPRESSION; NEUTROPHIL INFILTRATION; MACROPHAGE-MIGRATION; ETHANOL EXPOSURE; MODULATION; ATTACHMENT;
D O I
10.1177/0192623309335633
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Our recent studies suggest that higher neutrophil infiltration in females correlates with increased hepatobiliary expression of osteopontin (OPN) in alcoholic steatohepatitis (ASH). The objective of this study was to understand the role of alcohol in altering estrogen levels in females by examining the effect of ethanol (EtOH) on the estrous cycle and then investigate the potential relationship between estradiol (E2) and hepatobiliary OPN expression in a female rat ASH model. Ovariectomized (OVX) and E2-implanted OVX rats in the ASH group were evaluated for OPN mRNA and protein expression. Low doses of E2 resulted in significant down-regulation of OPN protein and mRNA as compared to the OVX group. However, with increasing doses of E2, there was up-regulation of both OPN mRNA and protein. Osteopontin was localized primarily to the biliary epithelium. Liver injury assessed by serum ALT and histopathology revealed a pattern similar to OPN expression. In all groups, hepatic neutrophilic infiltration correlated positively with OPN expression. Based on these data, we conclude that in our ASH model, low doses of E2 appear to be hepatoprotective, whereas the protective effect appears to diminish with increasing doses of E2, although additional cause and effect studies are needed for confirmation.
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收藏
页码:492 / 501
页数:10
相关论文
共 45 条
[1]   Role of osteopontin in hepatic neutrophil infiltration during alcoholic steatohepatitis [J].
Apte, UM ;
Banerjee, A ;
McRee, R ;
Wellberg, E ;
Ramaiah, SK .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2005, 207 (01) :25-38
[2]   Estrogen modulates cutaneous wound healing by downregulating macrophage migration inhibitory factor [J].
Ashcroft, GS ;
Mills, SJ ;
Lei, KJ ;
Gibbons, L ;
Jeong, MJ ;
Taniguchi, M ;
Burow, M ;
Horan, MA ;
Wahl, SM ;
Nakayama, T .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (09) :1309-1318
[3]   Higher neutrophil infiltration mediated by osteopontin is a likely contributing factor to the increased susceptibility of females to alcoholic liver disease [J].
Banerjee, A ;
Apte, UM ;
Smith, R ;
Ramaiah, SK .
JOURNAL OF PATHOLOGY, 2006, 208 (04) :473-485
[4]   The temporal expression of osteopontin (SPP-1) in the rodent model of alcoholic steatohepatitis: A potential biomarker [J].
Banerjee, Atrayee ;
Burghardt, Robert C. ;
Johnson, Greg A. ;
White, Frankie J. ;
Ramaiah, Shashi K. .
TOXICOLOGIC PATHOLOGY, 2006, 34 (04) :373-384
[5]   Low-dose estrogen therapy ameliorates experimental autoimmune encephalomyelitis in two different inbred mouse strains [J].
Bebo, BF ;
Fyfe-Johnson, A ;
Adlard, K ;
Beam, AG ;
Vandenbark, AA ;
Offner, H .
JOURNAL OF IMMUNOLOGY, 2001, 166 (03) :2080-2089
[6]   THE MURINE GENE ENCODING SECRETED PHOSPHOPROTEIN-1 (OSTEOPONTIN) - PROMOTER STRUCTURE, ACTIVITY, AND INDUCTION INVIVO BY ESTROGEN AND PROGESTERONE [J].
CRAIG, AM ;
DENHARDT, DT .
GENE, 1991, 100 :163-171
[7]  
Denhardt DT, 1998, J CELL BIOCHEM, P92, DOI 10.1002/(SICI)1097-4644(1998)72:30/31+<92::AID-JCB13>3.0.CO
[8]  
2-A
[9]   Role of osteopontin in cellular signaling and toxicant injury [J].
Denhardt, DT ;
Giachelli, CM ;
Rittling, SR .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2001, 41 :723-749
[10]   Estrogen receptor α, not β, is a critical link in estradiol-mediated protection against brain injury [J].
Dubal, DB ;
Zhu, H ;
Yu, J ;
Rau, SW ;
Shughrue, PJ ;
Merchenthaler, I ;
Kindy, MS ;
Wise, PM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (04) :1952-1957