7 research outputs found
Klinische und experimentelle Thromboseforschung – Genetische Determinanten, molekulare Mechanismen und therapeutische Strategien bei thrombotischen Komplikationen
The HPA-1b (Pro33) Isoform of Platelet Integrin αIIbβ3 Is a Prothrombotic Variant: Characterization by Fluorescence Resonance Energy Transfer
The human platelet antigen-1b variant of β allosterically shifts the dynamic conformational equilibrium of this integrin toward the active state
Integrins are heterodimeric cell-adhesion receptors comprising α and β subunits. The human platelet antigen-1 (HPA-1) polymorphism in αIIbβ3 arises from a Leu→Pro exchange at residue 33 in the genu of the β3 subunit, resulting in Leu-33 (HPA-1a) or Pro-33 (HPA-1b) isoforms. Although clinical investigations have provided conflicting results, some studies have suggested that Pro-33 platelets exhibit increased thrombogenicity. Under flow-dynamic conditions, the Pro-33 variant displays prothrombotic properties, characterized by increased platelet adhesion, aggregate/thrombus formation, and outside-in signaling. However, the molecular events underlying this prothrombotic phenotype have remained elusive. As residue 33 is located > 80 Å away from extracellular binding sites or transmembrane domains, we hypothesized that the Leu→Pro exchange allosterically shifts the dynamic conformational equilibrium of αIIbβ3 toward an active state. Multiple microsecond-long, all-atom molecular dynamics simulations of the ectodomain of the Leu-33 and Pro-33 isoforms provided evidence that the Leu→Pro exchange weakens interdomain interactions at the genu and alters the structural dynamics of the integrin to a more unbent and splayed state. Using FRET analysis of fluorescent proteins fused with αIIbβ3 in transfected HEK293 cells, we found that the Pro-33 variant in its resting state displays a lower energy transfer than the Leu-33 isoform. This finding indicated a larger spatial separation of the cytoplasmic tails in the Pro-33 variant. Together, our results indicate that the Leu→Pro exchange allosterically shifts the dynamic conformational equilibrium of αIIbβ3 to a structural state closer to the active one, promoting the fully active state and fostering the prothrombotic phenotype of Pro-33 platelets
Improvement of the in vivo cellular repopulation of decellularized cardiovascular tissues by a detergent‐free, non‐proteolytic, actin‐disassembling regimen
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