SwePub
Sök i LIBRIS databas

  Extended search

onr:"swepub:oai:DiVA.org:umu-16656"
 

Search: onr:"swepub:oai:DiVA.org:umu-16656" > Streptococcal M5 pr...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist
  • Weineisen, MariaLund University,Lunds universitet,Medicinska fakulteten,Faculty of Medicine (author)

Streptococcal M5 protein prevents neutrophil phagocytosis by interfering with CD11b/CD18 receptor-mediated association and signaling.

  • Article/chapterEnglish2004

Publisher, publication year, extent ...

  • 2004
  • printrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:umu-16656
  • https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-16656URI
  • https://lup.lub.lu.se/record/121504URI

Supplementary language notes

  • Language:English
  • Summary in:English

Part of subdatabase

Classification

  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Group A streptococci (GAS) are common human pathogens that express major surface-associated virulence factors designated M proteins. In this study, we explored directly the cellular mechanisms behind their supposed ability to prevent phagocytosis. Isolated human neutrophils killed an M-negative GAS mutant (DeltaM5), but not the wild-type parent strain (M5). After 3 h, 3-4 times as many DeltaM5 as M5 bacteria were associated with the neutrophils, and more DeltaM5 than M5 bacteria were ingested. However, there was no statistically significant difference between DeltaM5 and M5 bacteria in regard to the percentage of the neutrophil-associated bacteria that were ingested, indicating that M5 protein prevents an adhesion receptor-dependent association with neutrophils and not the phagocytic machinery per se. Different Abs against CD11b/CD18 (CR3) blocked adhesion and killing of DeltaM5 bacteria, whereas the blocking of two other complement receptors, CD11c/CD18 (CR4) and CD35 (CR1), did not. The CD11b/CD18-mediated killing of DeltaM5 bacteria resulted in protein tyrosine phosphorylations and Cdc42 activation. Furthermore, inhibition of CD11b/CD18 receptor engagement or tyrosine kinase activity blocked the DeltaM5-induced activation of Cdc42 as well as the killing of these bacteria. We conclude that M5 protein interferes with the CD11b/CD18-dependent association between GAS and neutrophils, and thereby blocks subsequent ingestion of the bacteria.

Subject headings and genre

Added entries (persons, corporate bodies, meetings, titles ...)

  • Sjöbring, UlfLund University,Lunds universitet,Avdelningen för mikrobiologi, immunologi och glykobiologi - MIG,Institutionen för laboratoriemedicin,Medicinska fakulteten,Division of Microbiology, Immunology and Glycobiology - MIG,Department of Laboratory Medicine,Faculty of Medicine(Swepub:lu)mmb-usj (author)
  • Fällman, MariaUmeå universitet,Institutionen för molekylärbiologi (Medicinska fakulteten)(Swepub:umu)mafa0002 (author)
  • Andersson, TommyLund University,Lunds universitet,Experimentell patologi, Malmö,Forskargrupper vid Lunds universitet,Experimental Pathology, Malmö,Lund University Research Groups(Swepub:lu)expp-tan (author)
  • Lunds universitetMedicinska fakulteten (creator_code:org_t)

Related titles

  • In:J Immunol172:6, s. 3798-38070022-1767
  • In:Journal of Immunology172:6, s. 3798-38071550-6606

Internet link

Find in a library

  • J Immunol (Search for host publication in LIBRIS)

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Find more in SwePub

By the author/editor
Weineisen, Maria
Sjöbring, Ulf
Fällman, Maria
Andersson, Tommy
About the subject
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Basic Medicine
and Immunology in th ...
Articles in the publication
J Immunol
Journal of Immun ...
By the university
Umeå University
Lund University

Search outside SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view