CD3γ and CD3δ are two highly related components of the T cell receptor (TCR)–CD3 complex which is essential for the assembly and signal transduction of the T cell receptor on mature T cells. In gene knockout mice deficient in either CD3δ or CD3γ, early thymic development mediated by pre-TCR was either undisturbed or severely blocked, respectively, and small numbers of TCR-αβ+ T cells were detected in the periphery of both mice. γδ T cell development was either normal in CD3δ−/− mice or partially blocked in CD3γ−/− mice. To examine the collective role of CD3γ and CD3δ in the assembly and function of pre-TCR and in the development of γδ T cells, we generated a mouse strain with a disruption in both CD3γ and CD3δ genes (CD3γδ−/−). In contrast to mice deficient in either CD3γ or CD3δ chains, early thymic development mediated by pre-TCR is completely blocked, and TCR-αβ+ or TCR-γδ+ T cells were absent in the CD3γδ−/− mice. Taken together, these studies demonstrated that CD3γ and CD3δ play an essential, yet partially overlapping, role in the development of both αβ and γδ T cell lineages.
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5 October 1998
Brief Definitive Report|
October 05 1998
Essential and Partially Overlapping Role of CD3γ and CD3δ for Development of αβ and γδ T Lymphocytes
Baoping Wang,
Baoping Wang
From the *Division of Immunology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215; and the ‡Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115
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Ninghai Wang,
Ninghai Wang
From the *Division of Immunology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215; and the ‡Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115
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Mariolina Salio,
Mariolina Salio
From the *Division of Immunology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215; and the ‡Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115
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Deborah Allen,
Deborah Allen
From the *Division of Immunology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215; and the ‡Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115
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Jian She,
Jian She
From the *Division of Immunology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215; and the ‡Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115
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Cox Terhorst
Cox Terhorst
From the *Division of Immunology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215; and the ‡Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115
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Baoping Wang
From the *Division of Immunology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215; and the ‡Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115
Ninghai Wang
From the *Division of Immunology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215; and the ‡Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115
Mariolina Salio
From the *Division of Immunology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215; and the ‡Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115
Arlene Sharpe
Deborah Allen
From the *Division of Immunology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215; and the ‡Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115
Jian She
From the *Division of Immunology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215; and the ‡Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115
Cox Terhorst
From the *Division of Immunology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215; and the ‡Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115
Address correspondence to Cox Terhorst, Division of Immunology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215. Phone: 617-667-7147; Fax: 617-667-7140; E-mail: cterhors @bidmc.harvard.edu
Dr. Salio's current address is Basel Institute of Immunology, Basel, Switzerland.
The first two authors contributed equally to this work.
Received:
May 26 1998
Revision Received:
July 22 1998
Online ISSN: 1540-9538
Print ISSN: 0022-1007
1998
J Exp Med (1998) 188 (7): 1375–1380.
Article history
Received:
May 26 1998
Revision Received:
July 22 1998
Citation
Baoping Wang, Ninghai Wang, Mariolina Salio, Arlene Sharpe, Deborah Allen, Jian She, Cox Terhorst; Essential and Partially Overlapping Role of CD3γ and CD3δ for Development of αβ and γδ T Lymphocytes . J Exp Med 5 October 1998; 188 (7): 1375–1380. doi: https://doi.org/10.1084/jem.188.7.1375
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