PROTEASE NEXIN-2 AMYLOID BETA-PROTEIN PRECURSOR - A TIGHT-BINDING INHIBITOR OF COAGULATION FACTOR-IXA

Protease nexin-2/amyloid beta protein precursor (PN-2/AbetaPP) is an a bundant, secreted platelet protein which is a potent inhibitor of coag ulation Factor XIa. We examined other potential anticoagulant activiti es of PN-2/AbetaPP. Purified Kunitz protease inhibitor domain of PN-2 / AbetaPP and PN-2 / AbetaPP itself were found to prolong the coagulat ion time of plasma and pure Factor IXa. The Kunitz protease inhibitor domain also inhibited the ability of Factor IXa to activate Factor X. PN-2 /AbetaPP inhibited Factor IXa with a K(i) of 7.9 to 3.9 x 10(-11) M in the absence and presence of heparin, respectively. When the seco nd-order rate constant of PN-2/AbetaPP's inhibition of Factor IXa (2.7 x 10(8) M-1 min-1) was compared to that of antithrombin Ill (3.8 x 10 (6) M-1 min-1), PN-2/AbetaPP was at least a 71-fold more potent inhibi tor of Factor IXa than antithrombin III. PN-2/AbetaPP formed a complex with Factor IXa as detected by gel filtration and ELISA. The finding that PN-2/AbetaPP is a potent inhibitor of Factor IXa could help to ex plain the spontaneous intracerebral hemorrhages seen in patients with hereditary cerebral hemorrhage with amyloidosis Dutch-type where there is an extensive accumulation of PN-2/AbetaPP in their cerebral blood vessels.