Platelet actin nodules are podosome-like structures dependent on Wiskott-Aldrich syndrome protein and ARP2/3 complex


Autoria(s): Poulter, Natalie S.; Pollitt, Alice Y.; Davies, Amy; Malinova, Dessislava; Nash, Gerard B.; Hannon, Mike J.; Pikramenou, Zoe; Rappoport, Joshua Z.; Hartwig, John H.; Owen, Dylan M.; Thrasher, Adrian J.; Watson, Stephen P.; Thomas, Steven G.
Data(s)

01/06/2015

Resumo

The actin nodule is a novel F-actin structure present in platelets during early spreading. However, only limited detail is known regarding nodule organization and function. Here we use electron microscopy, SIM and dSTORM super-resolution, and live-cell TIRF microscopy to characterize the structural organization and signalling pathways associated with nodule formation. Nodules are composed of up to four actin-rich structures linked together by actin bundles. They are enriched in the adhesion-related proteins talin and vinculin, have a central core of tyrosine phosphorylated proteins and are depleted of integrins at the plasma membrane. Nodule formation is dependent on Wiskott-Aldrich syndrome protein (WASp) and the ARP2/3 complex. WASp(-/-) mouse blood displays impaired platelet aggregate formation at arteriolar shear rates. We propose actin nodules are platelet podosome-related structures required for platelet-platelet interaction and their absence contributes to the bleeding diathesis of Wiskott-Aldrich syndrome.

Formato

text

Identificador

http://centaur.reading.ac.uk/44786/1/Platelet%20actin%20nodules%20are%20podosome-like%20structures%20dependent%20on%20Wiskott-Aldrich%20syndrome%20protein%20and%20Arp23%20complex.pdf

Poulter, N. S., Pollitt, A. Y. <http://centaur.reading.ac.uk/view/creators/90006835.html>, Davies, A., Malinova, D., Nash, G. B., Hannon, M. J., Pikramenou, Z., Rappoport, J. Z., Hartwig, J. H., Owen, D. M., Thrasher, A. J., Watson, S. P. and Thomas, S. G. (2015) Platelet actin nodules are podosome-like structures dependent on Wiskott-Aldrich syndrome protein and ARP2/3 complex. Nature Communications, 6. 7254. ISSN 2041-1723 doi: 10.1038/ncomms8254 <http://dx.doi.org/10.1038/ncomms8254>

Idioma(s)

en

Publicador

Nature Publishing Group

Relação

http://centaur.reading.ac.uk/44786/

creatorInternal Pollitt, Alice Y.

10.1038/ncomms8254

Direitos

cc_by_4

Tipo

Article

PeerReviewed