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10.1016/j.jbc.2021.101315

http://scihub22266oqcxt.onion/10.1016/j.jbc.2021.101315
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suck abstract from ncbi


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pmid34678311      J+Biol+Chem 2021 ; 297 (5): 101315
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  • Intracellular receptor EPAC regulates von Willebrand factor secretion from endothelial cells in a PI3K-/eNOS-dependent manner during inflammation #MMPMID34678311
  • Xiao J; Zhang B; Su Z; Liu Y; Shelite TR; Chang Q; Qiu Y; Bei J; Wang P; Bukreyev A; Soong L; Jin Y; Ksiazek T; Gaitas A; Rossi SL; Zhou J; Laposata M; Saito TB; Gong B
  • J Biol Chem 2021[Nov]; 297 (5): 101315 PMID34678311show ga
  • Coagulopathy is associated with both inflammation and infection, including infections with novel severe acute respiratory syndrome coronavirus-2, the causative agent Coagulopathy is associated with both inflammation and infection, including infection with novel severe acute respiratory syndrome coronavirus-2, the causative agent of COVID-19. Clot formation is promoted via cAMP-mediated secretion of von Willebrand factor (vWF), which fine-tunes the process of hemostasis. The exchange protein directly activated by cAMP (EPAC) is a ubiquitously expressed intracellular cAMP receptor that plays a regulatory role in suppressing inflammation. To assess whether EPAC could regulate vWF release during inflammation, we utilized our EPAC1-null mouse model and revealed increased secretion of vWF in endotoxemic mice in the absence of the EPAC1 gene. Pharmacological inhibition of EPAC1 in vitro mimicked the EPAC1-/- phenotype. In addition, EPAC1 regulated tumor necrosis factor-alpha-triggered vWF secretion from human umbilical vein endothelial cells in a manner dependent upon inflammatory effector molecules PI3K and endothelial nitric oxide synthase. Furthermore, EPAC1 activation reduced inflammation-triggered vWF release, both in vivo and in vitro. Our data delineate a novel regulatory role for EPAC1 in vWF secretion and shed light on the potential development of new strategies to control thrombosis during inflammation.
  • |Animals[MESH]
  • |COVID-19/metabolism[MESH]
  • |Disease Models, Animal[MESH]
  • |Endothelial Cells/*metabolism[MESH]
  • |Guanine Nucleotide Exchange Factors/deficiency/genetics/*metabolism[MESH]
  • |Inflammation/metabolism[MESH]
  • |Mice[MESH]
  • |Mice, Knockout[MESH]
  • |Nitric Oxide Synthase Type III/*metabolism[MESH]
  • |Phosphatidylinositol 3-Kinases/*metabolism[MESH]


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