Medical Journals

Pneumolysin Causes Neuronal Cell Death Through Mitochondrial Damage.

Authors:
  • Braun Johann S
  • Hoffmann Olaf
  • Schickhaus Miriam
  • Freyer Dorette
  • Dagand Emilie
  • Bermpohl Daniela
  • Mitchell Tim J
  • Bechmann Ingo
  • Weber Joerg R

From: Department of Neurology, Charité Universitaetsmedizin Berlin, Berlin, Germany. johannb@uaeu.ac.ae

Infection and immunity

  • Publish Date: Sep 2007
  • ISSN: 0019-9567
  • Volume: 75
  • Issue: 9
  • Pages: 4245-54
  • Medium: Print
  • Language: English
  • Citation (JAMA): Braun Johann S, Hoffmann Olaf, Schickhaus Miriam, et al. Pneumolysin Causes Neuronal Cell Death Through Mitochondrial Damage.. Infect. Immun. Sep 2007;75:4245-54

Abstract

Bacterial toxins such as pneumolysin are key mediators of cytotoxicity in infections. Pneumolysin is a pore-forming toxin released by Streptococcus pneumoniae, the major cause of bacterial meningitis. We found that pneumolysin is the pneumococcal factor that accounts for the cell death pathways induced by live bacteria in primary neurons. The pore-forming activity of pneumolysin is essential for the induction of mitochondrial damage and apoptosis. Pneumolysin colocalized with mitochondrial membranes, altered the mitochondrial membrane potential, and caused the release of apoptosis-inducing factor and cell death. Pneumolysin induced neuronal apoptosis without activating caspase-1, -3, or -8. Wild-type pneumococci also induced apoptosis without activation of caspase-3, whereas pneumolysin-negative pneumococci activated caspase-3 through the release of bacterial hydrogen peroxide. Pneumolysin caused upregulation of X-chromosome-linked inhibitor of apoptosis protein and inhibited staurosporine-induced caspase activation, suggesting the presence of actively suppressive mechanisms on caspases. In conclusion, our results indicate additional functions of pneumolysin as a mitochondrial toxin and as a determinant of caspase-independent apoptosis. Considering this, blocking of pneumolysin may be a promising cytoprotective strategy in pneumococcal meningitis and other infections.

Mesh Headings (Keywords): Animals, Apoptosis, Bacterial Proteins, Calcium, Cell Death, Cells, Cultured, Membrane Potential, Mitochondrial, Mitochondria, Mitochondrial Membranes, Neurons, Rats, Reactive Oxygen Species, Signal Transduction, Streptococcus pneumoniae, Streptolysins, Up-Regulation


Check for Full Text / PubMed Unique Identifier (PMID): 17562768


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


Advertisements

About | Privacy Policy | Business Solutions | Advertise | Contact | Add Healia to your site

©2012. Healia / Meredith Corporation  

Use of this site constitutes acceptance of our Terms of Service and Privacy Policy. All content on this Web site, including medical opinion and any other health-related information, is for informational purposes only and should not be used for a specific diagnosis or individual treatment plan for any situation. Use of this site and the information contained herein does not create a doctor-patient relationship. Always seek the direct advice of your doctor in connection with any questions or issues you may have regarding your own health or the health of others.