ucsf banner
Helen Diller Family Compr Cancer Ctr
WILLIAM E. SEAMAN, MD

Professor, Medicine and Microbiology/Immunology, UCSF; Program Director, Sandler Program for Asthma Research
Member, UCSF Biomedical Sciences Graduate Program (BMS) and Herbert Boyer Program in Biological Sciences (PIBS)

CONTACT

bseaman@medicine.ucsf.edu
(415) 750-2104 (voice)
(415) 750-6920 (fax)

VAMC 111R, San Francisco, CA 94143

additional websites:

Seaman Faculty Profile

EDUCATION

Princeton University, Princeton, New Jersey, A.B., 1964, English (cum laude)
Harvard University, Boston, Massachusetts, M.D., 1969, Medicine (cum laude)

PROFESSIONAL EXPERIENCE

1969-70

Intern and resident, Massachusetts General Hospital, Boston, Ma

1971-74

Fellow, Arthritis and Rheumatism Branch, NIAMDD, NIH, Bethesda, MD

1974

Senior Resident in Medicine, Massachusetts General Hospital

1975

Chief Resident in Medicine, Massachusetts General Hospital

1976

Clinical Fellow in Rheumatology, Massachusetts General Hospital

1976-84

Assistant Professor of Medicine, University of California San Francisco

1978-2002

Staff Physician, San Francisco VA Medical Center

1981-1992

Chief, Arthritis/Immunology Section, San Francisco VA Medical Center

1984-1988

Associate Professor of Medicine and Microbiology, UCSF

1988-present

Professor of Medicine and Microbiology/Immunology, UCSF

1992-1999

Chief, Medical Service, San Francisco VA Medical Center

1999-present

Program Director, Sandler Program for Asthma Research

1999-present

Chief, Immunology Section, San Francisco VA Medical Center

2000-present

Director, Laboratory for the Development of Signaling Assays, Alliance for Cellular Signaling

SELECTED PUBLICATIONS

(selected from 78)

Seaman WE, Talal N, Herzenberg LA, Ledbetter JA: Surface antigens on mouse killer cells: Use of monoclonal antibodies to inhibit or to enrich cytotoxic activity. J Immunol 129:982-986, 1981.

Wofsy D, Kerger CE, Seaman WE: Monocytosis in the BXSB model for systemic lupus erythematosus. J Exp Med 159:629-634, 1984.

Wofsy D, Seaman WE: Successful treatment of autoimmunity in NZB/NZW mice with monoclonal antibody to L3T4. J Exp Med 161:378-391, 1985.

Wofsy D, Seaman WE: Reversal of advanced murine lupus in NZB/NZW F1 mice by treatment with monoclonal antibody to L3T4. J Immunol 138:3247-3253, 1987.

Seaman WE, Eriksson E, Dobrow R, Imboden JB: Inositol trisphosphate is generated by a rat natural killer cell tumor in response to target cells or to cross-linked monoclonal antibody OX-34: possible signalling role for the OX-34 determinant during activation by target cells. Proc Natl Acad Sci USA 84:4239-4243, 1987.

Carteron NL, Wofsy D, Seaman WE: Induction of immune tolerance during administration of monoclonal antibody to L3T4 does not depend on depletion of L3T4+ cells. J Immunol 140:713-716, 1988.

Seaman WE, Niemi EC, Stark MR, Goldfien RD, Pollock AS, Imboden JB: Molecular cloning of gp42, a cell-surface molecule that is selectively induced on rat natural killer cells by interleukin-2: Glycolipid membrane anchoring and capacity for transmembrane signaling, J Exp Med. 173:251-260, 1991.

Ryan JC, Niemi EC, Goldfien RD, Hiserodt JC, Seaman WE: NKR-P1, an activating molecule in RAT NK cells, stimulates phosphoinositide turnover and a rise in intracellular calcium. J Immunol 147:3244, 1991.

Yokoyama WM, Ryan JC, Hunter JJ, Smith HMC, Stark M, Seaman WE: cDNA cloning of mouse NKR-P1 and genetic linkage with Ly-49: Identification of a natural killer gene complex on mouse chromosome VI. J Immunol 147:3229, 1991.

Ryan JC, Turck J, Niemi EC, Yokoyama WM, Seaman WE: Molecular cloning of the NK1.1 antigen, a member of the NKR-P1 family of natural killer cell activation molecules. J Immunol. 149:1631-1635, 1992.

Yokoyama WM, Seaman WE: The Ly-49 and NKR-P1 gene families encoding lectin-like receptors on natural killer cells: The NK Gene Complex. Ann Rev Immunol II 613-635, 1993.

Daniels BF, Nakamura MC, Rosen S, Yokoyama W, Seaman WE: Ly-49, a receptor for H-2Dd, has a functional carbohydrate recognition domain. Immunity 1:785-792, 1994.

Ryan JC, Niemi EC, Nakamura MC, Seaman WE: NKR-P1A is a target-specific receptor that activates natural killer cell cytotoxicity. J Exp Med 181:1911-1915, 1995.

Nakamura MC, Niemi EC, Fisher MJ, Shultz LD, Seaman WE, Ryan J. Mouse Ly-49A interrupts early signaling events in NK cell cytotoxicity and functionally associates with the SHP-1 tyrosine phosphatase. J Exp Med 185:673, 1997.

Nakamura, MC, Linnemeyer, PA, Niemi EC, Mason,L., Ortaldo JR, Ryan JC, Seaman WE: Mouse Ly-49D recognizes H-2Dd and activates natural killer cell cytotoxicity. J Exp Med, 189:493-500, 1999.

Seaman WE. Natural killer cells and natural killer T cells. Arthritis Rheum 43:1204-17, 2000.

Nakamura MC, Hayashi S, Niemi EC, Ryan JC, Seaman, WE: Activating Ly-49D and inhibitory Ly-49A NK cell receptors demonstrate distinct requirements for interaction with H2-Dd. J Exp Med 7:192:447-54, 2000.

Daws MR, Lanier LL, Seaman WE, Ryan JC: Cloning and characterization of a novel mouse myeloid DAP12-associated receptor family. Eur J Immunol 31:783-91, 2001.

Chung DH, Seaman WE, Daws MR. Characterization of TREM-3, an activating receptor on mouse macrophages: definition of a family of single Ig domain receptors on mouse chromosome 17. Eur J Immunol 32:59-66, 2002.

Gilman AG, Simon MI, Bourne HR, et al. Overview of the Alliance for Cellular Signaling. Nature 420:703-6, 2002.

Daws MR, Sullam PM, Niemi EC, Chen TT, Seaman WE. Pattern recognition by TREM-2: binding of anionic ligands. J Immunol. 171:594-9, 2003.

Chung DH, Humphrey MB, Nakamura MC, Ginzinger DG, Seaman WE, Daws MR. CMRF-35-like molecule-1, a novel mouse myeloid receptor, can inhibit osteoclast formation. J Immunol. 171:6541-8, 2003.

Chen TT, Brown EJ, Huang EJ, Seaman WE. Expression and function of SIRP- on astrocytomas. Cancer Res. 64:117-27, 2004.

Xhu X, Hart R, Chang MS, et al. Analysis of the major patterns of B cell gene expression changes in response to short-term stimulation with 33 single ligands. J Immunol. In Press, 2004.

3/15/05

This site will look much better in a browser that supports web standards, but it is accessible to any browser or Internet device. Please upgrade your browser.