Skip to main content
Top
Published in: World Journal of Surgery 2/2011

01-02-2011

Preoperative Toll-like Receptor Expression in Monocytes is Associated with Host Immunological Responses Following Gastrointestinal Surgery

Authors: Satoshi Ono, Hironori Tsujimoto, Shu-ichi Hiraki, Manabu Kinoshita, Kazuo Hase

Published in: World Journal of Surgery | Issue 2/2011

Login to get access

Abstract

Background

The present study was designed to evaluate the relationship between preoperative Toll-like receptor (TLR) expression in peripheral blood monocytes (PBMC) and the postoperative inflammatory cytokine secretion from PBMC, as well as the postoperative infectious complications in patients with gastrointestinal cancer.

Methods

Peripheral blood monocytes were isolated from 26 patients on the preoperative day and on postoperative day 1 (POD1). The monocytes were stained for CD14, TLR2, and TLR4 surface expression and stimulated ex vivo with lipopolysaccharide (LPS), after which the culture supernatant tumor necrosis factor alpha (TNFα), interleukin (IL)-1β, and interferon gamma (IFNγ) concentrations were measured in the culture supernatant. Postoperative clinical courses were monitored.

Results

There was a significant positive correlation between preoperative TLR4 expression and clinical stage in patients with gastrointestinal cancer. A significant negative correlation between preoperative TLR2 or TLR4 expression and the preoperative TNFα and IL-1β production was found. Furthermore, there was a significant negative correlation between preoperative TLR2 or TLR4 expression and postoperative inflammatory cytokine production.

Conclusions

Preoperative high expression of TLR on monocytes reduces the capacity for LPS-induced inflammatory cytokine production from monocytes. An analysis of preoperative TLR expression may therefore help to elucidate the systemic immunological response and the clinical course following gastrointestinal surgery.
Literature
1.
go back to reference Aosasa S, Ono S, Mochizuki H et al (2000) Activation of monocytes and endothelial cells depends on the severity of surgical stress. World J Surg 24:10–16CrossRefPubMed Aosasa S, Ono S, Mochizuki H et al (2000) Activation of monocytes and endothelial cells depends on the severity of surgical stress. World J Surg 24:10–16CrossRefPubMed
2.
go back to reference Ikuta S, Ono S, Kinoshita M et al (2003) Interleukin-18 concentration in the peritoneal fluid correlates with the severity of peritonitis. Am J Surg 185:550–555CrossRefPubMed Ikuta S, Ono S, Kinoshita M et al (2003) Interleukin-18 concentration in the peritoneal fluid correlates with the severity of peritonitis. Am J Surg 185:550–555CrossRefPubMed
3.
go back to reference Bone RC (1996) Toward a theory regarding the pathogenesis of the systemic inflammatory response syndrome: what we do and do not know about cytokine regulation. Crit Care Med 24:163–172CrossRefPubMed Bone RC (1996) Toward a theory regarding the pathogenesis of the systemic inflammatory response syndrome: what we do and do not know about cytokine regulation. Crit Care Med 24:163–172CrossRefPubMed
4.
go back to reference Wang SY, Mak KL, Chen LY et al (1992) Heterogeneity of human blood monocyte: two subpopulations with different sizes, phenotypes and functions. Immunology 77:298–303PubMed Wang SY, Mak KL, Chen LY et al (1992) Heterogeneity of human blood monocyte: two subpopulations with different sizes, phenotypes and functions. Immunology 77:298–303PubMed
5.
go back to reference Fingerle-Rowson G, Angstwurm M, Andreesen R et al (1998) Selective depletion of CD14+ CD16+ monocytes by glucocorticoid therapy. Clin Exp Immunol 112:501–506CrossRefPubMed Fingerle-Rowson G, Angstwurm M, Andreesen R et al (1998) Selective depletion of CD14+ CD16+ monocytes by glucocorticoid therapy. Clin Exp Immunol 112:501–506CrossRefPubMed
6.
go back to reference Medzhitov R, Janeway CA Jr (1997) Innate immunity: the virtues of a nonclonal system of recognition. Cell 91:295–298CrossRefPubMed Medzhitov R, Janeway CA Jr (1997) Innate immunity: the virtues of a nonclonal system of recognition. Cell 91:295–298CrossRefPubMed
7.
go back to reference Ulevitch RJ, Tobias PS (1995) Receptor-dependent mechanisms of cell stimulation by bacterial endotoxin. Annu Rev Immunol 13:437–457CrossRefPubMed Ulevitch RJ, Tobias PS (1995) Receptor-dependent mechanisms of cell stimulation by bacterial endotoxin. Annu Rev Immunol 13:437–457CrossRefPubMed
8.
go back to reference Takeshita F, Leifer CA, Gursel I et al (2001) Cutting edge: role of Toll-like receptor 9 in CpG DNA-induced activation of human cells. J Immunol 167:3555–3558PubMed Takeshita F, Leifer CA, Gursel I et al (2001) Cutting edge: role of Toll-like receptor 9 in CpG DNA-induced activation of human cells. J Immunol 167:3555–3558PubMed
9.
go back to reference Schwandner R, Dziarski R, Wesche H et al (1999) Peptidoglycan- and lipoteichoic acid-induced cell activation is mediated by toll-like receptor 2. J Biol Chem 274:17406–17409CrossRefPubMed Schwandner R, Dziarski R, Wesche H et al (1999) Peptidoglycan- and lipoteichoic acid-induced cell activation is mediated by toll-like receptor 2. J Biol Chem 274:17406–17409CrossRefPubMed
10.
go back to reference Yang H, Young DW, Gusovsky F et al (2000) Cellular events mediated by lipopolysaccharide-stimulated Toll-like receptor 4. MD-2 is required for activation of mitogen-activated protein kinases and Elk-1. J Biol Chem 275:20861–20866CrossRefPubMed Yang H, Young DW, Gusovsky F et al (2000) Cellular events mediated by lipopolysaccharide-stimulated Toll-like receptor 4. MD-2 is required for activation of mitogen-activated protein kinases and Elk-1. J Biol Chem 275:20861–20866CrossRefPubMed
11.
go back to reference Arbour NC, Lorenz E, Schutte BC et al (2000) TLR4 mutations are associated with endotoxin hyporesponsiveness in humans. Nat Genet 25:187–191CrossRefPubMed Arbour NC, Lorenz E, Schutte BC et al (2000) TLR4 mutations are associated with endotoxin hyporesponsiveness in humans. Nat Genet 25:187–191CrossRefPubMed
12.
go back to reference Park JS, Svetkauskaite D, He Q et al (2004) Involvement of Toll-like receptors 2 and 4 in cellular activation by high mobility group box 1 protein. J Biol Chem 279:7370–7377CrossRefPubMed Park JS, Svetkauskaite D, He Q et al (2004) Involvement of Toll-like receptors 2 and 4 in cellular activation by high mobility group box 1 protein. J Biol Chem 279:7370–7377CrossRefPubMed
13.
go back to reference Sasu S, LaVerda D, Qureshi N et al (2001) Chlamydia pneumoniae and chlamydial heat shock protein 60 stimulate proliferation of human vascular smooth muscle cells via toll-like receptor 4 and p44/p42 mitogen-activated protein kinase activation. Circ Res 89:244–250CrossRefPubMed Sasu S, LaVerda D, Qureshi N et al (2001) Chlamydia pneumoniae and chlamydial heat shock protein 60 stimulate proliferation of human vascular smooth muscle cells via toll-like receptor 4 and p44/p42 mitogen-activated protein kinase activation. Circ Res 89:244–250CrossRefPubMed
14.
go back to reference Devaney JM, Greene CM, Taggart CC et al (2003) Neutrophil elastase up-regulates interleukin-8 via toll-like receptor 4. FEBS Lett 544:129–132CrossRefPubMed Devaney JM, Greene CM, Taggart CC et al (2003) Neutrophil elastase up-regulates interleukin-8 via toll-like receptor 4. FEBS Lett 544:129–132CrossRefPubMed
15.
go back to reference Smiley ST, King JA, Hancock WW (2001) Fibrinogen stimulates macrophage chemokine secretion through toll-like receptor 4. J Immunol 167:2887–2894PubMed Smiley ST, King JA, Hancock WW (2001) Fibrinogen stimulates macrophage chemokine secretion through toll-like receptor 4. J Immunol 167:2887–2894PubMed
16.
go back to reference Sobin LH, Fleming ID (1997) TNM classification of malignant tumors, fifth edition, Union Internationale Contre le Cancer and the American Joint Committee on Cancer. Cancer 80:1803–1804CrossRefPubMed Sobin LH, Fleming ID (1997) TNM classification of malignant tumors, fifth edition, Union Internationale Contre le Cancer and the American Joint Committee on Cancer. Cancer 80:1803–1804CrossRefPubMed
17.
go back to reference Hoffmann JA, Kafatos FC, Janeway CA et al (1999) Phylogenetic perspective in innate immunity. Science 284:1313–1318CrossRefPubMed Hoffmann JA, Kafatos FC, Janeway CA et al (1999) Phylogenetic perspective in innate immunity. Science 284:1313–1318CrossRefPubMed
19.
go back to reference Chow JC, Young DW, Golenbock DT et al (1999) Toll-like receptor-4 mediates lipopolysaccharide-induced signal transduction. J Biol Chem 274:10689–10692CrossRefPubMed Chow JC, Young DW, Golenbock DT et al (1999) Toll-like receptor-4 mediates lipopolysaccharide-induced signal transduction. J Biol Chem 274:10689–10692CrossRefPubMed
20.
go back to reference Lein E, Sellati TJ, Yoshimura A et al (1999) Toll-like receptor-2 functions as a pattern recognition receptor for diverse bacterial products. J Biol Chem 274:33419–33425CrossRef Lein E, Sellati TJ, Yoshimura A et al (1999) Toll-like receptor-2 functions as a pattern recognition receptor for diverse bacterial products. J Biol Chem 274:33419–33425CrossRef
21.
go back to reference Dziarski R, Wang O, Miyake K et al (2001) MD-2 enables Toll-like receptor 2 mediated response to lipopolysaccharide and enhances TLR-2 mediated responses to Gram-positive and Gram-negative bacteria and their cell wall components. J Immunol 166:1938–1944PubMed Dziarski R, Wang O, Miyake K et al (2001) MD-2 enables Toll-like receptor 2 mediated response to lipopolysaccharide and enhances TLR-2 mediated responses to Gram-positive and Gram-negative bacteria and their cell wall components. J Immunol 166:1938–1944PubMed
22.
go back to reference Tsujimoto H, Ono S, Majima T et al (2006) Differential Toll-like receptor expression after ex vivo lipopolysaccharide exposure in patients with sepsis and following surgical stress. Clin Immunol 119:180–187CrossRefPubMed Tsujimoto H, Ono S, Majima T et al (2006) Differential Toll-like receptor expression after ex vivo lipopolysaccharide exposure in patients with sepsis and following surgical stress. Clin Immunol 119:180–187CrossRefPubMed
23.
go back to reference Tsujimoto H, Ono S, Efron PA et al (2008) Role of Toll-like receptor in the development of sepsis. Shock 29:315–321PubMed Tsujimoto H, Ono S, Efron PA et al (2008) Role of Toll-like receptor in the development of sepsis. Shock 29:315–321PubMed
24.
go back to reference McCall CE, Grosso-Wilmoth LM, LaRue K et al (1993) Tolerance to endotoxin-induced expression of the interleukin-1 beta gene in blood neutrophils of humans with the sepsis syndrome. J Clin Invest 91:853–861CrossRefPubMed McCall CE, Grosso-Wilmoth LM, LaRue K et al (1993) Tolerance to endotoxin-induced expression of the interleukin-1 beta gene in blood neutrophils of humans with the sepsis syndrome. J Clin Invest 91:853–861CrossRefPubMed
25.
go back to reference Calvano JE, Agnese DM, Um JY et al (2003) Modulation of the lipopolysaccharide receptor complex (CD14, TLR4, MD-2) and Toll-like receptor 2 in systemic inflammatory response syndrome-positive patients with and without infection: relationship to tolerance. Shock 20:415–419CrossRefPubMed Calvano JE, Agnese DM, Um JY et al (2003) Modulation of the lipopolysaccharide receptor complex (CD14, TLR4, MD-2) and Toll-like receptor 2 in systemic inflammatory response syndrome-positive patients with and without infection: relationship to tolerance. Shock 20:415–419CrossRefPubMed
26.
go back to reference Armstrong L, Medford AR, Hunter KJ et al (2004) Differential expression of Toll-like receptor (TLR)-2 and TLR-4 on monocytes in human sepsis. Clin Exp Immunol 136:312–319CrossRefPubMed Armstrong L, Medford AR, Hunter KJ et al (2004) Differential expression of Toll-like receptor (TLR)-2 and TLR-4 on monocytes in human sepsis. Clin Exp Immunol 136:312–319CrossRefPubMed
Metadata
Title
Preoperative Toll-like Receptor Expression in Monocytes is Associated with Host Immunological Responses Following Gastrointestinal Surgery
Authors
Satoshi Ono
Hironori Tsujimoto
Shu-ichi Hiraki
Manabu Kinoshita
Kazuo Hase
Publication date
01-02-2011
Publisher
Springer-Verlag
Published in
World Journal of Surgery / Issue 2/2011
Print ISSN: 0364-2313
Electronic ISSN: 1432-2323
DOI
https://doi.org/10.1007/s00268-010-0839-z

Other articles of this Issue 2/2011

World Journal of Surgery 2/2011 Go to the issue