Literature DB >> 8277203

Cellular distribution of endotoxin after injection of chemically purified lipopolysaccharide differs from that after injection of live bacteria.

Y Ge1, R M Ezzell, R G Tompkins, H S Warren.   

Abstract

Lipopolysaccharide (LPS) chemically extracted from gram-negative bacteria is often used in animal models to study endotoxemia. Laser confocal microscopy and immunofluorescence staining for comparison of injections of live Escherichia coli O111:B4 bacteria with LPS extracted from the same strain showed that cellular localization and time course in rat organs were markedly different after the two injections. Fluorescent staining and image analysis software allowed quantitative comparison of LPS within tissues at different times and doses. Antigenic LPS was detected in all tissues 1 hour after injection of both bacteria and LPS and was present in liver and spleen over the 28-day study period. Whole bacteria were identified in tissue macrophages for the first 48 h after injection; later, bacterial cell walls were replaced by diffuse antigenic material throughout the cytoplasm. Antigenic LPS was localized within hepatocytes only after injection of chemically purified LPS. Cellular localization of LPS in tissues is dependent on the form injected. Animal models that use purified LPS may not be representative of gram-negative bacteremia.

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Year:  1994        PMID: 8277203     DOI: 10.1093/infdis/169.1.95

Source DB:  PubMed          Journal:  J Infect Dis        ISSN: 0022-1899            Impact factor:   5.226


  20 in total

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3.  Hepatic uptake and deacylation of the LPS in bloodborne LPS-lipoprotein complexes.

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5.  Febrile-range temperature modifies early systemic tumor necrosis factor alpha expression in mice challenged with bacterial endotoxin.

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Review 6.  Endotoxin elimination in sepsis: physiology and therapeutic application.

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8.  Interaction of platelet-activating factor, spleen and atrial natriuretic peptide in plasma volume regulation during endotoxaemia in rats.

Authors:  X W Qu; R A Rozenfeld; W Huang; S E Crawford; F Gonzalez-Crussi; W Hsueh
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9.  Beta2-integrin-induced p38 MAPK activation is a key mediator in the CD14/TLR4/MD2-dependent uptake of lipopolysaccharide by hepatocytes.

Authors:  Melanie J Scott; Timothy R Billiar
Journal:  J Biol Chem       Date:  2008-08-13       Impact factor: 5.157

10.  Interleukin 10 reduces mortality from severe peritonitis in mice.

Authors:  T Kato; A Murata; H Ishida; H Toda; N Tanaka; H Hayashida; M Monden; N Matsuura
Journal:  Antimicrob Agents Chemother       Date:  1995-06       Impact factor: 5.191

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