A mechanism for hereditary angioedema with normal C1 inhibitor: an inhibitory regulatory role for the factor XII heavy chain

Blood. 2019 Mar 7;133(10):1152-1163. doi: 10.1182/blood-2018-06-860270. Epub 2018 Dec 27.

Abstract

The plasma proteins factor XII (FXII) and prekallikrein (PK) undergo reciprocal activation to the proteases FXIIa and kallikrein by a process that is enhanced by surfaces (contact activation) and regulated by the serpin C1 inhibitor. Kallikrein cleaves high-molecular-weight kininogen (HK), releasing the vasoactive peptide bradykinin. Patients with hereditary angioedema (HAE) experience episodes of soft tissue swelling as a consequence of unregulated kallikrein activity or increased prekallikrein activation. Although most HAE cases are caused by reduced plasma C1-inhibitor activity, HAE has been linked to lysine/arginine substitutions for Thr309 in FXII (FXII-Lys/Arg309). Here, we show that FXII-Lys/Arg309 is susceptible to cleavage after residue 309 by coagulation proteases (thrombin and FXIa), resulting in generation of a truncated form of FXII (δFXII). The catalytic efficiency of δFXII activation by kallikrein is 15-fold greater than for full-length FXII. The enhanced rate of reciprocal activation of PK and δFXII in human plasma and in mice appears to overwhelm the normal inhibitory function of C1 inhibitor, leading to increased HK cleavage. In mice given human FXII-Lys/Arg309, induction of thrombin generation by infusion of tissue factor results in enhanced HK cleavage as a consequence of δFXII formation. The effects of δFXII in vitro and in vivo are reproduced when wild-type FXII is bound by an antibody to the FXII heavy chain (HC; 15H8). The results contribute to our understanding of the predisposition of patients carrying FXII-Lys/Arg309 to angioedema after trauma, and reveal a regulatory function for the FXII HC that normally limits PK activation in plasma.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Angioedemas, Hereditary
  • Animals
  • Arginine / chemistry
  • Blood Coagulation
  • Bradykinin / blood
  • Catalysis
  • Complement C1 Inhibitor Protein / chemistry
  • Factor XII / chemistry*
  • Factor XIIa / chemistry
  • Factor XIa / chemistry*
  • HEK293 Cells
  • Hereditary Angioedema Type III / blood*
  • Hereditary Angioedema Type III / genetics*
  • Humans
  • Kininogens / blood
  • Lysine / chemistry
  • Mice
  • Mice, Inbred C57BL
  • Plasma Kallikrein / chemistry
  • Prekallikrein / chemistry
  • Protein Binding
  • Recombinant Proteins / chemistry
  • Surface Properties
  • Thrombin / genetics

Substances

  • Complement C1 Inhibitor Protein
  • Kininogens
  • Recombinant Proteins
  • SERPING1 protein, human
  • Serping1 protein, mouse
  • kininogen 1, human
  • Factor XII
  • Prekallikrein
  • Arginine
  • Factor XIa
  • Plasma Kallikrein
  • Factor XIIa
  • Thrombin
  • Lysine
  • Bradykinin