Literature DB >> 7751010

L-rhamnose inhibits proliferation of murine splenocytes by the lipopolysaccharide and polysaccharide moiety of Shigella dysenteriae type 1 lipopolysaccharide.

T Biswas1, S Roy, K K Banerjee.   

Abstract

The induction of proliferation of murine splenocytes by lipopolysaccharide (LPS) of Shigella dysenteriae type 1 and its polysaccharide (PS) and lipid A fractions was investigated. The LPS-induced proliferation reached a maximum at a concentration of 30 ng/ml. The PS and lipid A induced proliferation of murine splenocytes at similar concentrations. Preincubation of murine splenocytes with varying concentrations of L-rhamnose blocked LPS- and PS-induced proliferation in a dose-dependent manner. The lipid A-induced stimulation, on the contrary, was not affected by preincubation of the cells with L-rhamnose. These data suggest that activation of splenocytes by LPS and PS is mechanistically different from that induced by lipid A and is presumably involved in the specific recognition of carbohydrate structures on LPS and PS.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7751010      PMCID: PMC1415105     

Source DB:  PubMed          Journal:  Immunology        ISSN: 0019-2805            Impact factor:   7.397


  15 in total

1.  Identification and characterization of lipopolysaccharide-binding proteins on human peripheral blood cell populations.

Authors:  J L Halling; D R Hamill; M G Lei; D C Morrison
Journal:  Infect Immun       Date:  1992-03       Impact factor: 3.441

2.  Detection of lipopolysaccharide-binding proteins on membranes of murine lymphocyte and macrophage-like cell lines.

Authors:  T Kirikae; F Kirikae; F U Schade; M Yoshida; S Kondo; K Hisatsune; S Nishikawa; E T Rietschel
Journal:  FEMS Microbiol Immunol       Date:  1991-11

3.  A modification of the Lowry procedure to simplify protein determination in membrane and lipoprotein samples.

Authors:  M A Markwell; S M Haas; L L Bieber; N E Tolbert
Journal:  Anal Biochem       Date:  1978-06-15       Impact factor: 3.365

4.  Measurement of growth and viability of cells in culture.

Authors:  M K Patterson
Journal:  Methods Enzymol       Date:  1979       Impact factor: 1.600

5.  Elucidation of the structure of the Pasteurella haemolytica serotype T10 lipopolysaccharide O-antigen by n.m.r. spectroscopy.

Authors:  J C Richards; R A Leitch
Journal:  Carbohydr Res       Date:  1989-03-15       Impact factor: 2.104

Review 6.  Structural requirements of lipid A for endotoxicity and other biological activities.

Authors:  H Takada; S Kotani
Journal:  Crit Rev Microbiol       Date:  1989       Impact factor: 7.624

7.  Activation of lymphocytes of normal and tumor bearing mice by mangiferin, a naturally occurring glucosylxanthone.

Authors:  U Chattopadhyay; S Das; S Guha; S Ghosal
Journal:  Cancer Lett       Date:  1987-11       Impact factor: 8.679

8.  Blastogenesis and polyclonal immunoglobulin synthesis in murine spleen cells stimulated with lipopolysaccharide, lipid A and acid-degraded polysaccharide from Fusobacterium nucleatum.

Authors:  K Sveen; T Hofstad
Journal:  FEMS Microbiol Immunol       Date:  1990-05

9.  Specific endotoxic lipopolysaccharide-binding proteins on murine splenocytes. I. Detection of lipopolysaccharide-binding sites on splenocytes and splenocyte subpopulations.

Authors:  M G Lei; D C Morrison
Journal:  J Immunol       Date:  1988-08-01       Impact factor: 5.422

10.  Persistence of segregated phospholipid domains in phospholipid--lipopolysaccharide mixed bilayers: studies with spin-labeled phospholipids.

Authors:  Y Takeuchi; H Nikaido
Journal:  Biochemistry       Date:  1981-02-03       Impact factor: 3.162

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.