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

Human complement in the arachidonic acid transformation pathway in platelets

M J Polley, R L Nachman, B B Weksler

    The Journal of Experimental Medicine
    |February 1, 1981
    PubMed
    Summary

    Complement components C5-C9 enhance serotonin and thromboxane B2 release from platelets. This process, involving the membrane attack complex (C5b-9), can occur independently of classical or alternative complement pathways.

    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

    Protective effect of the multitarget compound DPH-4 on human SSAO/VAP-1-expressing hCMEC/D3 cells under oxygen-glucose deprivation conditions: an in vitro experimental model of cerebral ischaemia.

    British journal of pharmacology·2015
    Same author

    Psychometric properties of the QuickPIPER: a shortened version of the PIPER Fatigue scale.

    European journal of cancer care·2013
    Same author

    BBB on chip: microfluidic platform to mechanically and biochemically modulate blood-brain barrier function.

    Biomedical microdevices·2012
    Same author

    Patient experience of acupuncture provision in a GP practice.

    Complementary therapies in clinical practice·2012
    Same author

    Differential activation of mitochondrial apoptotic pathways by vasculotropic amyloid-beta variants in cells composing the cerebral vessel walls.

    FASEB journal : official publication of the Federation of American Societies for Experimental Biology·2009
    Same author

    Review article: the pathophysiology of thrombocytopenia in hepatitis C virus infection and chronic liver disease.

    Alimentary pharmacology & therapeutics·2007

    Area of Science:

    • Immunology
    • Biochemistry
    • Platelet Biology

    Background:

    • Platelets play a crucial role in hemostasis and inflammation.
    • Complement system activation can influence platelet function.
    • Arachidonic acid metabolism in platelets generates important signaling molecules like thromboxane B2.

    Purpose of the Study:

    • To investigate the role of complement components in arachidonate-mediated serotonin and thromboxane B2 release from platelets.
    • To determine the specific complement components involved in this process.
    • To elucidate the mechanism by which complement modulates platelet activation.

    Main Methods:

    • Utilized purified complement components (C5-C9) and platelet membranes.
    • Measured the release of 14C serotonin and thromboxane B2 (TXB2) in response to arachidonate.

    Related Experiment Videos

  • Analyzed the formation and characteristics of the membrane attack complex (C5b-9) on platelet surfaces.
  • Main Results:

    • Complement components C5-C9 significantly enhanced arachidonate-induced serotonin and TXB2 release.
    • This enhancement occurred independently of classical or alternative complement pathway activation and C3.
    • The membrane attack complex (C5b-9) was formed on platelet surfaces, suggesting its involvement in the observed reactivity.
    • Platelet membrane-bound complement components were essential for modulating serotonin release in the absence of exogenous complement.

    Conclusions:

    • The terminal complement components (C5-C9) are sufficient to enhance arachidonate-mediated platelet serotonin and TXB2 production.
    • The membrane attack complex (C5b-9) formation on platelets is a key event in this process.
    • While C3 may be involved in initial arachidonic acid mobilization, C5-C9 are critical for modulating the subsequent pathway leading to TXB2 production.