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PMID: 8612135 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Resistance to endotoxin shock and reduced dissemination of gram-negative bacteria in CD14-deficient mice.

Immunity ·Vol. 4 ·No. 4 ·1996-04-00 ·Pages 407-14

Haziot A, Ferrero E, Köntgen F, Hijiya N, Yamamoto S, Silver J, Stewart CL, Goyert SM

Abstract

Endotoxin shock is the result of activation of the immune system by endotoxin/LPS, a component of Gram-negative bacteria. CD14, a GPI-anchored glycoprotein expressed strongly by monocyte/macrophages, is one of several receptors for endotoxin/LPS. The role of CD14 in bacterial-induced and LPS-induced shock was tested in CD14-deficient mice produced by gene targeting in embryonic stem cells. CD14-deficient mice were found to be highly resistant to shock induced by either live Gram-negative bacteria or LPS; however, at very high concentrations of LPS or bacteria, responses through non-CD14 receptors could be detected. Surprisingly, CD14-deficient mice also showed dramatically reduced levels of bacteremia, suggesting an unexpected role for CD14 in the dissemination of Gram-negative bacteria.

MeSH Terms
Animals Cytokines/biosynthesis Escherichia coli Infections/genetics,immunology,prevention & control Gene Targeting Lipopolysaccharide Receptors/genetics,metabolism Lipopolysaccharides/toxicity Mice Mice, Inbred C57BL Mice, Knockout Monocytes/drug effects,immunology Shock, Septic/genetics,immunology,prevention & control
Chemicals
Cytokines Lipopolysaccharide Receptors Lipopolysaccharides
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Haziot A
Division of Molecular Medicine, North Shore University Hospital, Cornell University Medical College, Manhasset, New York 11030, USA.
Ferrero E
Köntgen F
Hijiya N
Yamamoto S
Silver J
Stewart C L
Goyert S M
Article Info
Journal
Immunity
Abbr.
Immunity
ISSN
1074-7613
Published
1996-04-00
Pages
407-14
Language
English
Region
United States
NLM ID
9432918
Subset
IM
Grants
NIAID NIH HHS · AI23859 · United States
NIGMS NIH HHS · GM47175 · United States
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