A decrease in thrombocyte count was observed in (NZW x BXSB)F1 (W/B F1) mice at the age of greater than 5 mo, whereas megakaryocyte counts were found to increase in such mice. FACS analyses revealed the presence of both platelet-associated antibodies (PAA) and circulating antiplatelet antibodies. There is a correlation between the presence of these antibodies and the degree of thrombocytopenia. The transplantation of normal bone marrow cells from BALB/c nu/nu mice to W/B F1 mice was found to have preventative and curative effects on thrombocytopenia; the mice showed normal platelet counts and no evidence of circulating antiplatelet antibodies. These results indicate that thrombocytopenia in W/B F1 mice is due to the presence of antibodies to platelets. We therefore think that W/B F1 mice serve as a useful animal model of idiopathic thrombocytopenic purpura (ITP) not only for elucidating the mechanism of the development of antiplatelet antibodies, but also for characterizing autoantibodies to platelets.
Article|
June 01 1988
(NZW x BXSB)F1 mouse. A new animal model of idiopathic thrombocytopenic purpura.
N Oyaizu,
N Oyaizu
Department of Pathology, Kansai Medical University, Osaka, Japan.
Search for other works by this author on:
R Yasumizu,
R Yasumizu
Department of Pathology, Kansai Medical University, Osaka, Japan.
Search for other works by this author on:
M Miyama-Inaba,
M Miyama-Inaba
Department of Pathology, Kansai Medical University, Osaka, Japan.
Search for other works by this author on:
S Nomura,
S Nomura
Department of Pathology, Kansai Medical University, Osaka, Japan.
Search for other works by this author on:
H Yoshida,
H Yoshida
Department of Pathology, Kansai Medical University, Osaka, Japan.
Search for other works by this author on:
S Miyawaki,
S Miyawaki
Department of Pathology, Kansai Medical University, Osaka, Japan.
Search for other works by this author on:
Y Shibata,
Y Shibata
Department of Pathology, Kansai Medical University, Osaka, Japan.
Search for other works by this author on:
S Mitsuoka,
S Mitsuoka
Department of Pathology, Kansai Medical University, Osaka, Japan.
Search for other works by this author on:
K Yasunaga,
K Yasunaga
Department of Pathology, Kansai Medical University, Osaka, Japan.
Search for other works by this author on:
S Morii
S Morii
Department of Pathology, Kansai Medical University, Osaka, Japan.
Search for other works by this author on:
N Oyaizu
Department of Pathology, Kansai Medical University, Osaka, Japan.
R Yasumizu
Department of Pathology, Kansai Medical University, Osaka, Japan.
M Miyama-Inaba
Department of Pathology, Kansai Medical University, Osaka, Japan.
S Nomura
Department of Pathology, Kansai Medical University, Osaka, Japan.
H Yoshida
Department of Pathology, Kansai Medical University, Osaka, Japan.
S Miyawaki
Department of Pathology, Kansai Medical University, Osaka, Japan.
Y Shibata
Department of Pathology, Kansai Medical University, Osaka, Japan.
S Mitsuoka
Department of Pathology, Kansai Medical University, Osaka, Japan.
K Yasunaga
Department of Pathology, Kansai Medical University, Osaka, Japan.
S Morii
Department of Pathology, Kansai Medical University, Osaka, Japan.
Online ISSN: 1540-9538
Print ISSN: 0022-1007
J Exp Med (1988) 167 (6): 2017–2022.
Citation
N Oyaizu, R Yasumizu, M Miyama-Inaba, S Nomura, H Yoshida, S Miyawaki, Y Shibata, S Mitsuoka, K Yasunaga, S Morii; (NZW x BXSB)F1 mouse. A new animal model of idiopathic thrombocytopenic purpura.. J Exp Med 1 June 1988; 167 (6): 2017–2022. doi: https://doi.org/10.1084/jem.167.6.2017
Download citation file: