TY - JOUR
T1 - Flow cytometric determination of intracytoplasmic Wiskott-Aldrich syndrome protein in peripheral blood lymphocyte subpopulations
AU - Kawai, S.
AU - Minegishi, M.
AU - Ohashi, Y.
AU - Sasahara, Y.
AU - Kumaki, S.
AU - Konno, T.
AU - Miki, H.
AU - Derry, J.
AU - Nonoyama, S.
AU - Miyawaki, T.
AU - Horibe, K.
AU - Tachibana, N.
AU - Kudoh, E.
AU - Yoshimura, Y.
AU - Izumikawa, Y.
AU - Sako, M.
AU - Tsuchiya, S.
N1 - Funding Information:
This work was supported in part by grant-in-aid for Scientific Research from the Ministry of Education, Science, Sports and Culture, Japan.
PY - 2002/2/1
Y1 - 2002/2/1
N2 - We have produced a novel monoclonal antibody (mAb) directed against Wiskott-Aldrich syndrome protein (WASP) by immunizing mice with the recombinant protein. The mAb designated 5A5 is highly specific to WASP and suitable for Western blot analysis and immunoprecipitation. A flow cytometric assay using the 5A5 mAb identifies expression of intracytoplasmic WASP in lymphocytes from normal individuals. Double staining analysis with cell surface CD3, CD19, and CD56, and intracytoplasmic molecules revealed WASP expression in each subpopulation. With regard to WASP expression in patients with Wiskott-Aldrich syndrome (WAS) and X-linked thrombocytopenia (XLT), peripheral blood mononuclear cells (PBMCs) from nine patients and Epstein-Barr virus-transformed B-lymphoblastoid cell lines from seven patients examined did not show WASP expression by flow cytometric analysis. These results were confirmed by Western blot analysis. We conclude that WASP expression in lymphocyte subpopulations from patients with WAS and XLT can be more precisely evaluated by flow cytometry as compared with Western blot analysis. This flow cytometry method is important as a supplement to Western blots, but even more important as an alternative and powerful assay that can contribute to research on WASP as well as diagnosis in a clinical setting.
AB - We have produced a novel monoclonal antibody (mAb) directed against Wiskott-Aldrich syndrome protein (WASP) by immunizing mice with the recombinant protein. The mAb designated 5A5 is highly specific to WASP and suitable for Western blot analysis and immunoprecipitation. A flow cytometric assay using the 5A5 mAb identifies expression of intracytoplasmic WASP in lymphocytes from normal individuals. Double staining analysis with cell surface CD3, CD19, and CD56, and intracytoplasmic molecules revealed WASP expression in each subpopulation. With regard to WASP expression in patients with Wiskott-Aldrich syndrome (WAS) and X-linked thrombocytopenia (XLT), peripheral blood mononuclear cells (PBMCs) from nine patients and Epstein-Barr virus-transformed B-lymphoblastoid cell lines from seven patients examined did not show WASP expression by flow cytometric analysis. These results were confirmed by Western blot analysis. We conclude that WASP expression in lymphocyte subpopulations from patients with WAS and XLT can be more precisely evaluated by flow cytometry as compared with Western blot analysis. This flow cytometry method is important as a supplement to Western blots, but even more important as an alternative and powerful assay that can contribute to research on WASP as well as diagnosis in a clinical setting.
KW - Flow cytometry
KW - Monoclonal antibody
KW - WASP
KW - Wiskott-Aldrich syndrome
KW - X-linked thrombocytopenia
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U2 - 10.1016/S0022-1759(01)00549-X
DO - 10.1016/S0022-1759(01)00549-X
M3 - Article
C2 - 11792389
AN - SCOPUS:0036469993
SN - 0022-1759
VL - 260
SP - 195
EP - 205
JO - Journal of Immunological Methods
JF - Journal of Immunological Methods
IS - 1-2
ER -