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Vascular ATP Diphosphohydrolase (CD39/ATPDase)

  • Chapter
Ecto-ATPases

Abstract

Circulatory homeostasis is usually maintained by quiescent endothelial cells that possess highly effective anticoagulant and platelet thromboregulatory mechanisms. Following injury, the vascular endothelium is considered to undergo a process of activation where cells are exposed to oxidative stress, lose intrinsic antithrombotic properties and become procoagulant and facilitative for platelet aggregation. Endothelial cells express an ATPDase that hydrolyzes extracellular adenosine nucleotides and can inhibit stimulated human platelet aggregation in vitro. Loss of this ectoenzyme activity with reduced membrane protein expression occurs shortly following TNFα stimulation or perturbation of endothelial cells by reactive oxygen species in vitro. Comparable events follow reperfusion injury and xenograft rejection in vivo. Additionally, the administration of antioxidants and purified apyrases ameliorate rat renal reperfusion injury and discordant xenograft rejection, respectively.

Following our identification of the gene encoding vascular ATPDase as CD39, we are now examining the pathophysiological significance of the expression of CD39/ATPDase by the vasculature and how this enzymatic function is modulated by inflammatory processes. This work will be facilitated by the generation of knock-out and CD39 transgenic mice. Our approach should provide a closer understanding of thrombosis and vascular disruption in the context of transplant vascular pathobiology and other inflammatory diseases characterized by vascular thrombosis and platelet activation.

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Kaczmarek, E. et al. (1997). Vascular ATP Diphosphohydrolase (CD39/ATPDase). In: Plesner, L., Kirley, T.L., Knowles, A.F. (eds) Ecto-ATPases. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-5955-9_22

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