Thromb Haemost 2010; 104(01): 105-117
DOI: 10.1160/TH09-10-0715
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

Determination of a factor VIII-interactive region within plasmin responsible for plasmin-catalysed activation and inactivation of factor VIII(a)[*]

Katsumi Nishiya
1   Department of Pediatrics, Nara Medical University, Kashihara, Nara, Japan
,
Keiji Nogami
1   Department of Pediatrics, Nara Medical University, Kashihara, Nara, Japan
,
Kiyotaka Okada
2   Department of Physiology, Kinki University School of Medicine, Osaka, Japan
,
Osamu Matsuo
2   Department of Physiology, Kinki University School of Medicine, Osaka, Japan
,
Masahiro Takeyama
1   Department of Pediatrics, Nara Medical University, Kashihara, Nara, Japan
,
Kenichi Ogiwara
1   Department of Pediatrics, Nara Medical University, Kashihara, Nara, Japan
,
Midori Shima
1   Department of Pediatrics, Nara Medical University, Kashihara, Nara, Japan
› Author Affiliations
Further Information

Publication History

Received: 21 October 2009

Accepted after major revision: 25 February 2010

Publication Date:
15 December 2017 (online)

Summary

Plasmin, an active form of plasminogen, activates and inactivates factor VIII (FVIII) by limited proteolysis. We have previously identifiedly sine-binding site-independent plasmin-interactive sites on the FVIII A2 domain responsible for cleavages at Arg336 and Arg372, together with lysine-binding site-dependent plasmin sites on the light chain responsible for cleavage at Lys36. We have now characterised FVIII-interactive regions on plasmin. SDS-PAGE analysis demonstrated that a monoclon al antibody (mAb) against kringle (K)5-catalytic domain (K5-CD) of plasmin significantly blocked plasmin-catalysed cleavages at Arg336 and Arg372. K5-CD fragment and this mAb blocked plasmincatalysed activation and inactivation of FVIII(a). Anti-K1–2–3 and anti-K4 mAbs blocked plasmin-catalysed cleavages at Lys36, and K1–2–3 and K4 fragments inhibited plasmin-catalysed inactivation of A11–336 FVIIIa. The K5-CD preferentially bound to the A2 domain (Kd app ; 52 nM), whilst the K1–2–3 and K4 bound to the light chain (Kd app; 75 and 106 nM, respectively) in ELISA. Binding was attributed to the A2 484–509 region and A3 1690–1705/1804–1818 region, respectively. 6-aminohexanoic acid, a lysine analogue, significantly inhibited the light chain/K1–2–3 (and K4) binding by ∼90%, whilst A2/K5-CD binding was moderated by only ∼35%. Furthermore, an anti-CD antibody blocked plasmin-catalysed cleavage by inhibiting the A2/K5-CD interaction. These data demon strate that the K5-CD of plasmin (and plasminogen) interacts with the A2 domain independent of lysine-binding site, whilst interactions of K1–2–3 and K4 with the light chain are lysine-binding site-dependent. Interactions between the K5-CD and A2 likely constitute the major regulatory mechanism for activation and inactivation of FVIII(a) mediated by cleavage at Arg372 and Arg336.

* An account of this work was presented at the 49th annual meeting of the American Society of Hematology, 2007, Atlanta, GA. This work was partly supported by grants for MEXT KAKENHI 21591370 and The Mother and Child Health Foundation in Japan.


 
  • References

  • 1 van Wersch JW, Tjwa MK. Coagulation/fibrinolysis balance and lung cancer. Hemostasis 1991; 21: 117-123.
  • 2 Bick RL, Arun B, and Frenkel EP. Disseminated intravascular coagulation. clinical and pathophysiological mechanisms and manifestations. Hemostasis 1999; 29: 111-134.
  • 3 Bachmann F. Plasminogen-plasmin enzyme system. Hemostasis and Thrombosis 4th Ed. Churchill Livingstone, New York, 2000; 275-320.
  • 4 Loy JA, Lin X, Schenone M. et al Domain interactions between streptokinase and human plasminogen. Biochemistry 2001; 40: 14686-14695.
  • 5 Nogami K, Shima M, Matsumoto T. et al Mechanisms of plasmin-catalyzed inactivation of factor VIII. A crucial role for proteolytic cleavage at Arg336 responsible for plasmincatalyzed factor VIII inactivation. J Biol Chem 2007; 282: 5287-5295.
  • 6 Zeibdawi AR, Pryzdial EL. Mechanism of factor Va inactivation by plasmin. Loss of A2 and A3 domains from a Ca2+-dependent complex of fragments bound to phospholipid. J Biol Chem 2001; 276: 19929-19936.
  • 7 Samis JA, Ramsey GD, Walker JB. et al Proteolytic processing of human coagulation factor IX by plasmin. Blood 2000; 95: 943-951.
  • 8 Pryzdial EL, Lavigne N, Dupuis N. et al Plasmin converts factor X from coagulation zymogen to fibrinolysis cofactor. J Biol Chem 1999; 274: 8500-8505.
  • 9 Mann KG, Nesheim ME, Church WR. et al Surface-dependent reactions of the vitamin K-dependent enzyme complexes. Blood 1990; 76: 1-16.
  • 10 Wood I W, Capon DJ, Simonsen CC. et al Expression of active human factor VIII from recombinant DNA clones. Nature 1984; 312: 330-337.
  • 11 Eaton D, Rodriguez H, Vehar GA. Proteolytic processing of human factor VIII. Correlation of specific cleavages by thrombin, factor Xa, and activated protein C with activation and inactivation of factor VIII coagulant activity. Biochemistry 1986; 25: 505-512.
  • 12 Fay PJ. Activation of factor VIII and mechanisms of cofactor action. Blood Rev 2004; 18: 1-15.
  • 13 Lamphear BJ, Fay PJ. Proteolytic interactions of factor IXa with human factor VIII and factor VIIIa. Blood 1992; 80: 3120-3126.
  • 14 Nogami K, Wakabayashi H, Schmidt K. et al Altered interactions between the A1 and A2 subunits of factor VIIIa following cleavage of A1 subunit by factor Xa. J Biol Chem 2003; 278: 1634-1641.
  • 15 Nogami K, Nishiya K, Saenko EL. et al Identification of a plasmin-interactive site within the A2 domain of the factor VIII heavy chain. Biochim Biophys Acta 2008; 1784: 53-63.
  • 16 Nogami K, Nishiya K, Saenko EL. et al Identification of plasmin-interactive sites in the light chain of factor VIII responsible for proteolytic cleavage at Lys36. J Biol Chem 2009; 284: 6934-6945.
  • 17 Okada K, Ueshima S, Kawao N. et al Binding of plasminogen to hepatocytes isolated from injured mouse liver and nonparenchymal-cell-dependent proliferation of hepatocytes. Blood Coagul Fibrinolysis 2008; 19: 503-511.
  • 18 Mimms LT, Zampighi G, Nozaki Y. et al Phospholipid vesicle formation and transmembrane protein incorporation using octyl glucoside. Biochemistry 1981; 20: 833-840.
  • 19 Shima M, Scandella D, Yoshioka A. et al A factor VIII neutralizing monoclonal antibody and a human inhibitor alloantibody recognizing epitopes in the C2 domain inhibit factor VIII binding to von Willebrand factor and to phosphatidylserine. Thromb Haemost 1993; 69: 240-246.
  • 20 Okada K, Ueshima S, Matsuno H. et al Effect of staphylokinase-derived non-adecapeptide on the activation of plasminogen. Thromb Haemost 2007; 97: 795-802.
  • 21 Lollar P, Fay PJ, Fass DN. Factor VIII and factor VIIIa. Methods Enzymol 1993; 222: 128-143.
  • 22 Nogami K, Zhou Q, Myles T. et al Exosite-interactive regions in the A1 and A2 domains of factor VIII facilitate thrombin-catalyzed cleavage of heavy chain. J Biol Chem 2005; 280: 18476-18487.
  • 23 Chang Y, Mochalkin I, McCance SG. et al Structure and ligand binding determinants of the recombinant kringle 5 domain of human plasminogen. Biochemistry 1998; 37: 3258-3271.
  • 24 Thorsen S, Clemmensen I, Sottrup-Jensen M. et al Adsorption to fibrin of native fragments of known primary structure from human plasminogen. Biochim Biophys Acta 1981; 668: 377-387.
  • 25 Rejante M, Elliott Jr BW, Llinas M. A 1H-NMR study of plasminogen kringle 4 interactions with intact and partially digested fibrinogen. Fibrinolysis 1991; 05: 87-92.
  • 26 Lerch PG, Rickli EE, Lergier W. et al Localization of individual lysine-binding regions in human plasminogen and investigations on their complex-forming properties. Eur J Biochem 1980; 107: 7-13.
  • 27 McCance SG, Menhart N, Castellino FJ. Amino acid residues of the kringle-4 and kringle-5 domains of human plasminogen that stabilize their interactions with omega-amino acid ligands. J Biol Chem 1994; 269: 32405-32410.
  • 28 Nogami K, Wakabayashi H, Fay PJ. Mechanisms of factor Xa-catalyzed cleavage of the factor VIIIa A1 subunit resulting in cofactor inactivation. J Biol Chem 2003; 278: 16502-16509.
  • 29 Nogami K, Lapan KA, Zhou Q. et al Identification of a factor Xa-interactive site within residues 337–372 of the factor VIII heavy chain. J Biol Chem 2004; 279: 15763-15771.
  • 30 Shen BW, Spiegel PC, Chang CH. et al The tertiary structure and domain organization of coagulation factor VIII. Blood 2008; 111: 200-208.
  • 31 Ngo JC, Huang M, Roth DA. et al Crystal structure of human factor VIII: implications for the formation of the factor IXa-factor VIIIa complex. Structure 2008; 16: 597-606.
  • 32 Varfaj F, Neuberg J, Jenkins PV. et al Role of P1 residues Arg336 and Arg562 in the activated-Protein-C-catalysed inactivation of Factor VIIIa. Biochem J 2006; 396: 355-362.
  • 33 Lenting PJ, Donath MJ, van Mourik JA. et al Identification of a binding site for blood coagulation factor IXa on the light chain of human factor VIII. J Biol Chem 1994; 269: 7150-7155.
  • 34 Fay PJ, Koshibu K. The A2 subunit of factor VIIIa modulates the active site of factor IXa. J Biol Chem 1991; 266: 2172-2177.