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

Studies on glomerular immune solubilization by complement in patients with IgA nephropathy.

Y Tomino1, H Sakai, A J Woodroffe

  • 1Department of Internal Medicine, School of Medicine, Tokai University, Kanagawa, Japan.

Acta Pathologica Japonica
|November 1, 1987
PubMed
Summary

Normal human serum effectively dissolves immune deposits in IgA nephropathy. This solubilization, crucial for understanding the disease, depends on active complement components, not isolated C3 or C4 proteins.

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

Restricted gammadelta T-cell receptor repertoire in IgA nephropathy renal biopsies.

Kidney international·2001
Same author

Excellent long-term graft survival in low risk, primary renal allografts treated with prednisolone-avoidance immunosuppression.

Clinical transplantation·2000
Same author

Poor recovery and short survival of infused factor X in a case of acquired factor X deficiency and amyloidosis.

Thrombosis and haemostasis·1999
Same author

Clozapine-induced acute interstitial nephritis.

Lancet (London, England)·1999
Same author

Progressive hepatic failure secondary to adult polycystic kidney disease.

Australian and New Zealand journal of medicine·1999
Same author

Renal biopsy precipitating catastrophic antiphospholipid syndrome, complicated by protein S deficiency and acute adrenal failure.

Australian and New Zealand journal of medicine·1999

Area of Science:

  • Nephrology
  • Immunology
  • Complement System Biology

Background:

  • Immunoglobulin A (IgA) nephropathy is characterized by immune deposits in the glomeruli.
  • The in-vivo mechanisms of solubilizing these glomerular immune deposits are not fully understood.
  • Understanding IgA nephropathy pathogenesis is critical for developing targeted therapies.

Purpose of the Study:

  • To investigate the capacity of human serum and complement components to solubilize glomerular immune deposits in IgA nephropathy.
  • To determine the role of specific complement components, such as C3 and C4, in this solubilization process.

Main Methods:

  • Renal biopsy specimens from 15 IgA nephropathy patients were used.
  • Specimens were incubated with fresh or heated normal human sera, or lyophilized C3/C4.

Related Experiment Videos

  • Fluorescence microscopy with FITC-labelled anti-human IgA was employed to assess immune deposit solubilization.
  • Main Results:

    • Fresh normal human sera demonstrated a significant ability to solubilize glomerular immune deposits.
    • Serum's solubilization capacity decreased after heat inactivation and absorption with anti-C3 antiserum.
    • Lyophilized C3 or C4 alone did not solubilize the immune deposits.

    Conclusions:

    • The solubilization of glomerular immune deposits in IgA nephropathy requires active, whole complement components.
    • The alternative pathway of complement appears to be involved in the solubilization process.
    • Isolated complement proteins (C3, C4) are insufficient for dissolving these immune deposits.