NR AUOI
AU Robertson,C.; Booth,S.A.; Beniac,D.R.; Coulthart,M.B.; Booth,T.F.; McNicol,A.
TI Cellular prion protein is released on exosomes from activated platelets
QU Blood 2006 May 15; 107(10): 3907-11
PT journal article
AB Cellular prion protein (PrPc) is a glycophosphatidylinositol (GPI)-anchored protein, of unknown function, found in a number of tissues throughout the body, including several blood components of which platelets constitute the largest reservoir in humans. It is widely believed that a misfolded, protease-resistant form of PrPc, PrPsc, is responsible for the transmissible spongiform encephalopathy (TSE) group of fatal neurodegenerative diseases. Although the pathogenesis of TSEs is poorly understood, it is known that PrPc must be present in order for the disease to progress; thus, it is important to determine the physiologic function of PrPc. Resolving the location of PrPc in blood will provide valuable clues as to its function. PrPc was previously shown to be on the alpha granule membrane of resting platelets. In the current study platelet activation led to the transient expression of PrPc on the platelet surface and its subsequent release on both microvesicles and exosomes. The presence of PrPc on platelet-derived exosomes suggests a possible mechanism for PrPc transport in blood and for cell-to-cell transmission.
MH Blood Platelets/*physiology/ultrastructure; Cell Membrane/ultrastructure; *Exocytosis; Flow Cytometry; Humans; Microscopy, Immunoelectron; Neurodegenerative Diseases/blood; *Platelet Activation; PrPc Proteins/*blood; Prion Diseases/blood
AD Catherine Robertson, Stephanie A. Booth (Stephanie_Booth@hc-sc.gc.ca), Daniel R. Beniac, Michael B. Coulthart, Timothy F. Booth, and Archibald McNicol mcnicol@ms.umanitoba.ca., Department of Oral Biology, University of Manitoba, 780 Bannatyne Avenue, Winnipeg, Manitoba, Canada R3E 0W2.
SP englisch
PO USA