Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Endotoxin-binding substances from human leukocytes and platelets.

G F Springer, J C Adye

    Infection and Immunity
    |November 1, 1975
    PubMed
    Summary
    This summary is machine-generated.

    Related Concept Videos

    You might also read

    Related Articles

    Articles linked to this work by shared authors, journal, and citation graph.

    Sort by
    Same author

    BLOOD GROUP ACTIVITY OF GRAM-NEGATIVE BACTERIA.

    The Journal of experimental medicine·2009
    Same author

    Specific role of T and Tn tumor-associated antigens in adhesion between a human breast carcinoma cell line and a normal human breast epithelial cell line.

    Japanese journal of cancer research : Gann·1999
    Same author

    T (Thomsen-Friedenreich) and Tn epitope location and their spatial relations to adhesion plaques on human breast carcinoma cells: immunogold-silver staining studies at scanning electron microscopic level.

    Journal of submicroscopic cytology and pathology·1998
    Same author

    Quantitative computerized image analysis of Tn and T (Thomsen-Friedenreich) epitopes in prognostication of human breast carcinoma.

    The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society·1997
    Same author

    Immunoreactive T and Tn epitopes in cancer diagnosis, prognosis, and immunotherapy.

    Journal of molecular medicine (Berlin, Germany)·1997
    Same author

    Immunoreactivities of polyclonal and monoclonal anti-T and anti-Tn antibodies with human carcinoma cells, grown in vitro and in a xenograft model.

    International journal of cancer·1997
    Same journal

    <i>Porphyromonas gingivalis</i> sphingolipids affect early responses of THP-1 macrophages to outer membrane vesicles.

    Infection and immunity·2026
    Same journal

    A genome-wide CRISPR screen defines host determinants of early <i>Brucella</i> infection in human macrophage-like cells.

    Infection and immunity·2026
    Same journal

    Antiphospholipid antibodies in acute and post-treatment Lyme disease.

    Infection and immunity·2026
    Same journal

    The cholesterol-dependent cytolysin promotes <i>Streptococcus</i> systemic spread and induces arachidonic acid accumulation-mediated lethality in a murine intraperitoneal infection model.

    Infection and immunity·2026
    Same journal

    Phenotypic and genotypic analysis of <i>Candida albicans</i> vaginal isolates reveals that <i>ECE1</i> expression underpins pathogenicity.

    Infection and immunity·2026
    Same journal

    <i>Staphylococcus aureus</i> pore-forming toxins differentially shape disease severity in experimental endophthalmitis.

    Infection and immunity·2026
    See all related articles

    Human immune cells like platelets and leukocytes bind toxic lipopolysaccharide (LPS). Lipid extracts from these cells, particularly glycerophosphatides, show significant LPS-binding activity, suggesting a role for lipids in endotoxin interaction.

    Area of Science:

    • Immunology
    • Biochemistry
    • Lipidomics

    Background:

    • Gram-negative bacteria produce toxic lipopolysaccharides (LPS).
    • Human blood cells, including platelets, granulocytes, and mononuclear leukocytes, interact with LPS.
    • Understanding LPS-binding mechanisms is crucial for immune response and therapeutic strategies.

    Purpose of the Study:

    • To identify and characterize the components within human platelets and leukocytes responsible for binding lipopolysaccharide.
    • To investigate the nature of endotoxin-binding activity in these cells.

    Main Methods:

    • Extraction of human platelets and leukocytes using n-butanol-water.
    • Analysis of the organic phase for endotoxin-binding activity.
    • Characterization of the chemical composition of active extracts using solubility and polyacrylamide gel electrophoresis.

    Related Experiment Videos

  • Testing of lipid A and its derivatives for inhibitory effects on endotoxin binding.
  • Main Results:

    • Whole human platelets, granulocytes, and mononuclear leukocytes exhibit high affinity for bacterial lipopolysaccharide.
    • Endotoxin-binding activity was localized to the n-butanol-water organic phase extract.
    • The most active components were glycerophosphatides, soluble in petroleum ether, indicating a lipidic nature.
    • Lipid A and its de-O-acylated derivative demonstrated significant inhibition of endotoxin binding to erythrocytes.

    Conclusions:

    • Lipids, particularly glycerophosphatides, are key components in human platelets and leukocytes responsible for binding bacterial lipopolysaccharide.
    • The lipid A moiety of endotoxins plays a critical role in the interaction with host cells.
    • These findings suggest a novel mechanism for endotoxin recognition and interaction involving cellular lipids.