Vwf K1362A resulted in failure of protein synthesis in mice

Naomi Sanda, Nobuaki Suzuki, Atsuo Suzuki, Takeshi Kanematsu, Mayuko Kishimoto, Hidetoshi Hasuwa, Akira Takagi, Tetsuhito Kojima, Tadashi Matsushita, Shigeo Nakamura

Research output: Contribution to journalArticle

Abstract

Von Willebrand factor (VWF) is synthesized in megakaryocytes and endothelial cells (ECs) and has two main roles: to carry and protect coagulation factor VIII (FVIII) from degradation by forming VWF–FVIII complex; and to mediate platelet adhesion and aggregation at sites of vascular injury. Previous research using the HEK293 cell line revealed that the VWF K1362 mutation interacted directly with platelet glycoprotein Ib (GPIb). Vwf K1362A knock-in (KI) mice were therefore generated to verify the in vivo function of residue 1362 in binding to platelet GPIb. The Cre-loxP system was employed to introduce the Vwf K1362A mutation systemically in mice. In blood coagulation analysis, the VWF antigen (VWF:Ag) of Lys1362Ala KI homozygous (homo) mice was below the sensitivity of detection by enzyme-linked immunosorbent assay. FVIII activities (FVIII:C) were 47.9 ± 0.3 and 3.3 ± 0.3% (K1362A heterozygous (hetero) and K1362A KI homo mice, respectively) compared to wild-type mice. Immunohistochemical staining analysis revealed that VWF protein did not exist in ECs of K1362A KI homo mice. These results indicated that VWF protein synthesis of K1362A was impaired after transcription in mice. K1362 seems to represent a very important position not only for VWF function, but also for VWF synthesis in mice.

Original languageEnglish
Pages (from-to)428-435
Number of pages8
JournalInternational Journal of Hematology
Volume107
Issue number4
DOIs
Publication statusPublished - 2018 Apr 1

Fingerprint

von Willebrand Factor
Proteins
Platelet Glycoprotein GPIb-IX Complex
Platelet Membrane Glycoproteins
Factor VIII
Endothelial Cells
Mutation
Megakaryocytes
HEK293 Cells
Vascular System Injuries
Blood Coagulation
Platelet Aggregation
Enzyme-Linked Immunosorbent Assay
Staining and Labeling
Cell Line

Keywords

  • Genetic mutation
  • Mouse model
  • Von Willebrand factor

ASJC Scopus subject areas

  • Hematology

Cite this

Sanda, N., Suzuki, N., Suzuki, A., Kanematsu, T., Kishimoto, M., Hasuwa, H., ... Nakamura, S. (2018). Vwf K1362A resulted in failure of protein synthesis in mice. International Journal of Hematology, 107(4), 428-435. https://doi.org/10.1007/s12185-017-2394-y

Vwf K1362A resulted in failure of protein synthesis in mice. / Sanda, Naomi; Suzuki, Nobuaki; Suzuki, Atsuo; Kanematsu, Takeshi; Kishimoto, Mayuko; Hasuwa, Hidetoshi; Takagi, Akira; Kojima, Tetsuhito; Matsushita, Tadashi; Nakamura, Shigeo.

In: International Journal of Hematology, Vol. 107, No. 4, 01.04.2018, p. 428-435.

Research output: Contribution to journalArticle

Sanda, N, Suzuki, N, Suzuki, A, Kanematsu, T, Kishimoto, M, Hasuwa, H, Takagi, A, Kojima, T, Matsushita, T & Nakamura, S 2018, 'Vwf K1362A resulted in failure of protein synthesis in mice', International Journal of Hematology, vol. 107, no. 4, pp. 428-435. https://doi.org/10.1007/s12185-017-2394-y
Sanda, Naomi ; Suzuki, Nobuaki ; Suzuki, Atsuo ; Kanematsu, Takeshi ; Kishimoto, Mayuko ; Hasuwa, Hidetoshi ; Takagi, Akira ; Kojima, Tetsuhito ; Matsushita, Tadashi ; Nakamura, Shigeo. / Vwf K1362A resulted in failure of protein synthesis in mice. In: International Journal of Hematology. 2018 ; Vol. 107, No. 4. pp. 428-435.
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AU - Suzuki, Nobuaki

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AU - Hasuwa, Hidetoshi

AU - Takagi, Akira

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AU - Nakamura, Shigeo

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