INTERACTIONS OF BLV GP30 WITH B CELL SIGNAL PATHWAYS
INTERACTIONS OF BLV GP30 WITH B CELL SIGNAL PATHWAYS
批准号:
2680029
负责人:
VALERIE T HAMILTON
金额:
$6.96万
依托单位国家:
美国
项目类别:
财政年份:
1998
资助国家:
美国
项目状态:
已结题
起止时间:
1998-07-01 至 2001-06-30
中文摘要
许多淋巴细胞增生性疾病都是由病毒引起的
英文摘要
Many lymphoproliferative disorders are known to result from viral
infection including infection by human T lymphotropic virus (HTLV) and
Epstein Barr virus. Bovine leukemia virus (BLV) is a retrovirus which
causes a nonneoplastic B lymphocyte proliferation in infected cattle
that may progress to lymphoma or leukemia and is closely related to HTLV
both genetically and in the initiation of lymphocyte proliferation. The
mechanism of proliferation has not been determined but is hypothesized
to result from viral protein perturbation of normal proliferative
pathways in the host cell. The goal of this project is to examine the
role of the BLV transmembrane protein, gp30, on host cell activation.
The BLV transmembrane protein, gp30, has sequence homology with the
normal signal transducers of both B and T cells. In in vitro studies,
chimeras of gp30 transduces activation signals from the cell surface,
and mutation of the gp30 protein has been shown to decrease viral
infectivity and proliferation in vivo. The proposed research will
attempt to identify the role of gp30 in signal transmission and B cell
activation. The hypothesis is that the BLV transmembrane protein gp30
initiates a tyrosine kinase signal pathway in infected host lymphocytes,
leading to increased host cell activation. Three specific aims will be
used to test the hypothesis: i) identifying specific tyrosine kinases
that interact with cytoplasmic gp30, ii) determine whether the levels
of gp30 expression correlate to the presence and increased activation
status of specific tyrosine kinases associated with gp30 and iii)
determining if the identified tyrosine kinases activate infected
lymphocytes. This research should provide insight into the mechanisms
of normal signal pathways in B cells as well as methods by which viruses
may subvert these mechanisms during infection. The candidate is a
veterinarian completing a comparative pathology residency and is
starting a Ph.D in comparative virology/immunology. The candidate has
completed the didactic phase of the Ph.D. including preparation of an
independent research proposal. The proposed project constitutes her
doctoral research and will provide direction for the long-term goal of
investigating mechanisms of viral/host interactions and cell regulation.
Washington State University and the Department of Veterinary
Microbiology and Pathology have a long history of successfully training
graduate students. The faculty includes numerous successful researchers
in the field of infectious diseases and students closely interact with
the researchers.
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INTERACTIONS OF BLV GP30 WITH B CELL SIGNAL PATHWAYS
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批准号:2886116
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项目类别:
-
资助金额:$7.19万
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财政年份:1998
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负责人:VALERIE T HAMILTON
-
依托单位:
INTERACTIONS OF BLV GP30 WITH B CELL SIGNAL PATHWAYS
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批准号:6168726
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项目类别:
-
资助金额:$7.52万
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财政年份:1998
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负责人:VALERIE T HAMILTON
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依托单位:
海外基金