Literature DB >> 32562089

Comparison of molecular structure and fibrin polymerization between two Bβ-chain N-terminal region fibrinogen variants, Bβp.G45C and Bβp.R74C.

Takahiro Kaido1, Masahiro Yoda1, Tomu Kamijo1, Chiaki Taira1, Yumiko Higuchi1, Nobuo Okumura2,3.   

Abstract

We identified two heterozygous dysfibrinogenemias, Bβp.Gly45Cys (Kyoto VII; K-VII) and Bβp.Arg74Cys (Iida II; I-II). The impairment of polymerization of Bβp.G45C has been well analyzed; however, that of Bβp.R74C has not. Thus, we compared fibrin polymerization between these variants. To determine the structural and functional characterization of purified fibrinogens, we performed immunoblotting analysis, kinetic analyses of fibrinopeptide A and B release, and thrombin- or batroxobin-catalyzed fibrin or fibrin monomer polymerization. Immunoblotting analysis showed that both variant fibrinogens had variant fibrinogen-albumin complexes and variant fibrinogen multimers, and the amounts of fibrinogen-albumin complexes with fibrinogen K-VII was more than with fibrinogen I-II. Moreover, fibrinopeptide B release from fibrinogen K-VII was about 50% of the control, whereas the others were normal. The maximum slopes of polymerization for variant fibrinogens were reduced, but fibrinogen K-VII was reduced more than fibrinogen I-II. The present study demonstrated that both Bβp.G45C and Bβp.R74C variants showed the presence of variant fibrinogen-albumin complexes and variant fibrinogen multimers, and polymerization of Bβp.G45C was impaired more than Bβp.R74C. Our study and several previous reports concerning the clinical phenotype of both variants suggested the risks of bleeding for patients with Bβp.G45C and thrombosis for patients with Bβp.R74C.

Entities:  

Keywords:  Albumin; Bβ N-terminal region; Congenital dysfibrinogenemia; Lateral aggregation

Year:  2020        PMID: 32562089     DOI: 10.1007/s12185-020-02919-5

Source DB:  PubMed          Journal:  Int J Hematol        ISSN: 0925-5710            Impact factor:   2.490


  3 in total

1.  A Novel Amino Acid Substitution, Fibrinogen Bβp.Pro234Leu, Associated with Hypofibrinogenemia Causing Impairment of Fibrinogen Assembly and Secretion.

Authors:  Takahiro Kaido; Masahiro Yoda; Tomu Kamijo; Shinpei Arai; Chiaki Taira; Yumiko Higuchi; Nobuo Okumura
Journal:  Int J Mol Sci       Date:  2020-12-10       Impact factor: 5.923

Review 2.  Heterogeneity of Genotype-Phenotype in Congenital Hypofibrinogenemia-A Review of Case Reports Associated with Bleeding and Thrombosis.

Authors:  Monika Brunclikova; Tomas Simurda; Jana Zolkova; Miroslava Sterankova; Ingrid Skornova; Miroslava Dobrotova; Zuzana Kolkova; Dusan Loderer; Marian Grendar; Jan Hudecek; Jan Stasko; Peter Kubisz
Journal:  J Clin Med       Date:  2022-02-18       Impact factor: 4.241

3.  Pediatric patient with fibrinogen Villeurbanne II presenting with an unprovoked portal vein thrombosis.

Authors:  Brenton J Francisco; Bal Krishan Sharma; Hannah M Russell; Leah Rosenfeldt; A Phillip Owens; Matthew J Flick; Eric S Mullins; Joseph Palumbo
Journal:  Blood Adv       Date:  2022-07-26
  3 in total

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