Desialylation accelerates platelet clearance after refrigeration and initiates GPIbα metalloproteinase-mediated cleavage in mice Article

cited authors

  • Jansen, AJG; Josefsson, EC; Rumjantseva, V; Liu, QP; Falet, H; Bergmeier, W; Cifuni, SM; Sackstein, R; Von Andrian, UH; Wagner, DD; Hartwig, JH; Hoffmeister, KM

fiu authors

abstract

  • When refrigerated platelets are rewarmed, they secrete active sialidases, including the lysosomal sialidase Neu1, and express surface Neu3 that remove sialic acid from platelet von Willebrand factor receptor (VWFR), specifically the GPIbα subunit. The recovery and circulation of refrigerated platelets is greatly improved by storage in the presence of inhibitors of sialidases. Desialylated VWFR is also a target for metalloproteinases (MPs), because GPIbα and GPV are cleaved from the surface of refrigerated platelets. Receptor shedding is inhibited by the MP inhibitor GM6001 and does not occur in Adam17ΔZn/ΔZn platelets expressing inactive ADAM17. Critically, desialylation in the absence of MP-mediated receptor shedding is sufficient to cause the rapid clearance of platelets from circulation. Desialylation of platelet VWFR therefore triggers platelet clearance and primes GPIbα and GPV for MP-dependent cleavage. © 2012 by The American Society of Hematology.

publication date

  • February 2, 2012

Digital Object Identifier (DOI)

start page

  • 1263

end page

  • 1273

volume

  • 119

issue

  • 5