The hepatocyte as a microbial product-responsive cell

被引:26
作者
Vodovotz, Y [1 ]
Liu, SB [1 ]
McCloskey, C [1 ]
Shapiro, R [1 ]
Green, A [1 ]
Billiar, TR [1 ]
机构
[1] Univ Pittsburgh, Dept Surg, Pittsburgh, PA 15213 USA
来源
JOURNAL OF ENDOTOXIN RESEARCH | 2001年 / 7卷 / 05期
关键词
D O I
10.1177/09680519010070050401
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
Much research has focused on the responses to microbial products of immune cells such as monocytes, macrophages, and neutrophils. Although the liver is a primary response organ in various infections, relatively little is known about the antimicrobial responses of its major cell type, the hepatocyte. It is now known that the recognition of bacteria occurs via cell-surface proteins that are members of the Toll-like receptor (TLR) family. In addition, lipopolysaccharide (LPS) is bound by circulating LPS-binding protein (LBP) and presented to cell-surface CD14, which in turn interacts with TLR and transduces an intracellular signal. We investigated the CD14 and TLR2 responses of whole liver and isolated hepatocytes, and demonstrated that these cells can be induced to express the molecules necessary for responses to both Gram-positive and Gram-negative bacteria. Our findings may have clinical implications for pathological states such as sepsis.
引用
收藏
页码:365 / 373
页数:9
相关论文
共 86 条
[1]  
ANDERSSON R, 1991, HEPATO-GASTROENTEROL, V38, P547
[2]   STIMULATION OF THE SYNTHESIS OF HISTAMINE AND PUTRESCINE IN MICE BY A PEPTIDOGLYCAN OF GRAM-POSITIVE BACTERIA [J].
ANDO, T ;
ENDO, Y ;
ABE, M ;
KUMAGAI, K .
MICROBIOLOGY AND IMMUNOLOGY, 1994, 38 (03) :209-215
[3]   Epidemiology of severe sepsis in the United States: Analysis of incidence, outcome, and associated costs of care [J].
Angus, DC ;
Linde-Zwirble, WT ;
Lidicker, J ;
Clermont, G ;
Carcillo, J ;
Pinsky, MR .
CRITICAL CARE MEDICINE, 2001, 29 (07) :1303-1310
[4]   INTESTINAL GRAM-NEGATIVE BACTERIAL OVERGROWTH INVIVO AUGMENTS THE INVITRO RESPONSE OF KUPFFER CELLS TO ENDOTOXIN [J].
BILLIAR, TR ;
MADDAUS, MA ;
WEST, MA ;
CURRAN, RD ;
WELLS, CA ;
SIMMONS, RL .
ANNALS OF SURGERY, 1988, 208 (04) :532-540
[5]   MECHANISMS OF HOST DEFENSE AGAINST INFECTION WITH STREPTOCOCCUS-PNEUMONIAE [J].
BRUYN, GAW ;
ZEGERS, BJM ;
VANFURTH, R .
CLINICAL INFECTIOUS DISEASES, 1992, 14 (01) :251-262
[6]   Nitric oxide synthase isoform III gene expression in rat liver is up-regulated by lipopolysaccharide and lipoteichoic acid [J].
Bucher, M ;
Ittner, KP ;
Zimmermann, M ;
Wolf, K ;
Hobbhahn, J ;
Kurtz, A .
FEBS LETTERS, 1997, 412 (03) :511-514
[7]   PARALLEL SIGNAL-PROCESSING AMONG MAMMALIAN MAPKS [J].
CANO, E ;
MAHADEVAN, LC .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (03) :117-122
[8]   PROTECTIVE EFFICACY OF DIFFERENT CELL-WALL FRACTIONS OF MYCOBACTERIUM-TUBERCULOSIS [J].
CHUGH, IB ;
KANSAL, R ;
VINAYAK, VK ;
KHULLER, GK .
FOLIA MICROBIOLOGICA, 1992, 37 (06) :407-412
[9]   M protein mediated adhesion of M type 24 Streptococcus pyogenes stimulates release of interleukin-6 by HEp-2 tissue culture cells [J].
Courtney, HS ;
Ofek, I ;
Hasty, DL .
FEMS MICROBIOLOGY LETTERS, 1997, 151 (01) :65-70
[10]   HEPATOCYTES PRODUCE NITROGEN-OXIDES FROM L-ARGININE IN RESPONSE TO INFLAMMATORY PRODUCTS OF KUPFFER CELLS [J].
CURRAN, RD ;
BILLIAR, TR ;
STUEHR, DJ ;
HOFMANN, K ;
SIMMONS, RL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (05) :1769-1774