Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1989 May;57(5):1556-60.
doi: 10.1128/iai.57.5.1556-1560.1989.

Role of lipopolysaccharide in induction of Ia expression during infection with gram-negative bacteria

Affiliations

Role of lipopolysaccharide in induction of Ia expression during infection with gram-negative bacteria

N E Marshall et al. Infect Immun. 1989 May.

Abstract

Lipopolysaccharide (LPS), a major component of the outer membrane of gram-negative bacteria, is known to be a potent modulator of many host immune functions, including the expression of products of the class II major histocompatibility locus (Ia molecules) by macrophages. LPS-mediated Ia induction is controlled by the lps gene. We sought to determine the role of LPS in the induction of Ia expression during infection with gram-negative bacteria. To address this question, we tested a simple prediction: if LPS is the primary determinant of Ia induction during gram-negative infection, then the Ia response to intraperitoneal injection of these organisms should be under the control of the lps gene. We found that while both LPS-responder and LPS-low-responder mice showed strong Ia responses to injection of either a gram-positive bacterium (Listeria monocytogenes) or concanavalin A, only the LPS-responder mice responded strongly to gram-negative organisms or to LPS alone. We interpret these results as strong evidence for the role of LPS as the primary determinant of Ia induction by gram-negative bacteria.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Exp Med. 1978 Jul 1;148(1):115-27 - PubMed
    1. Biochem J. 1963 Oct;89:114-23 - PubMed
    1. J Immunol. 1980 Jan;124(1):20-4 - PubMed
    1. Cell Immunol. 1980 Sep 1;54(2):487-90 - PubMed
    1. Infect Immun. 1982 Jan;35(1):52-7 - PubMed

Publication types

Substances