Literature DB >> 325138

The response of recombinant inbred strains of mice to bacterial lipopolysaccharides.

J Watson, R Riblet, B A Taylor.   

Abstract

Fourteen recombinant inbred strains of mice have been produced by the inbreeding of the F2 generation of a cross between C57BL/6J and C3H/HeJ progenitor mice. The responses of these BXH strains to bacterial lipopolysaccharides (LPS) have been characterized. Four BXH strains are high LPS responders and nine strains are low LPS responders. One BXH strain shows intermediate responsiveness which may reflect residual heterozygosity. F1 hybrid mice from low x high responder strains were intermediate in their response to LPS suggesting additive genetic control. The LPS responses in backcross mice from the F1 x low LPS responders showed segregation consistent with LPS responsiveness being determined by a single gene. In 13/14 BXH strains, there was concordant inheritance of LPS responsiveness and the major urinary protein locus Mup-1b. The association of the expression of the Mup-1 alleles with LPS responsiveness in the BXH strains suggests that the defective LPS response gene in C3H/HeJ mice is located on chromosome 4.

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Year:  1977        PMID: 325138

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  43 in total

Review 1.  Forward genetic dissection of innate response to infection in inbred mouse strains: selected success stories.

Authors:  S Gruenheid; P Gros
Journal:  Clin Exp Immunol       Date:  2010-12       Impact factor: 4.330

2.  Quantitative trait locus analysis using recombinant inbred intercrosses: theoretical and empirical considerations.

Authors:  Fei Zou; Jonathan A L Gelfond; David C Airey; Lu Lu; Kenneth F Manly; Robert W Williams; David W Threadgill
Journal:  Genetics       Date:  2005-05-06       Impact factor: 4.562

3.  Assessing the significance of quantitative trait loci in replicable mapping populations.

Authors:  Fei Zou; Zongli Xu; Todd Vision
Journal:  Genetics       Date:  2006-08-03       Impact factor: 4.562

Review 4.  Mouse chromosome 4.

Authors:  R Blank; J Eppig; F T Fiedorek; W N Frankel; J M Friedman; K Huppi; I Jackson; B Mock
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

5.  Difference in susceptibility to gram-negative urinary tract infection between C3H/HeJ and C3H/HeN mice.

Authors:  L Hagberg; R Hull; S Hull; J R McGhee; S M Michalek; C Svanborg Edén
Journal:  Infect Immun       Date:  1984-12       Impact factor: 3.441

6.  Dimethyl sulfoxide modulates NF-kappa B and cytokine activation in lipopolysaccharide-treated murine macrophages.

Authors:  K A Kelly; M R Hill; K Youkhana; F Wanker; J M Gimble
Journal:  Infect Immun       Date:  1994-08       Impact factor: 3.441

Review 7.  Genetics-squared: combining host and pathogen genetics in the analysis of innate immunity and bacterial virulence.

Authors:  Jenny Persson; Russell E Vance
Journal:  Immunogenetics       Date:  2007-09-14       Impact factor: 2.846

8.  Assay of locus-specific genetic load implicates rare Toll-like receptor 4 mutations in meningococcal susceptibility.

Authors:  Irina Smirnova; Navjiwan Mann; Annemiek Dols; H H Derkx; Martin L Hibberd; Michael Levin; Bruce Beutler
Journal:  Proc Natl Acad Sci U S A       Date:  2003-05-02       Impact factor: 11.205

9.  Genetic factors in host resistance to urinary tract infection.

Authors:  C Svanborg Edén; D Briles; L Hagberg; J McGhee; S Michalec
Journal:  Infection       Date:  1984 Mar-Apr       Impact factor: 3.553

10.  Selective reversal of H-2 linked genetic unresponsiveness to lysozymes. I. Non-H-2 gene(s) closely linked to the Ir-2 locus on chromosome 2 permit(s) an antilysozyme response in H-2b mice.

Authors:  S Sadegh-Nasseri; D E Kipp; B A Taylor; A Miller; E Sercarz
Journal:  Immunogenetics       Date:  1984       Impact factor: 2.846

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