INTERACTIONS OF BLV GP30 WITH B CELL SIGNAL PATHWAYS
INTERACTIONS OF BLV GP30 WITH B CELL SIGNAL PATHWAYS
批准号:
6168726
负责人:
VALERIE T HAMILTON
金额:
$7.52万
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 2002-06-30
中文摘要
点击翻译按钮获取中文摘要
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.
期刊论文(2)
专著(0)
科研奖励(0)
会议论文
Translocation of the B cell receptor to lipid rafts is inhibited in B cells from BLV-infected, persistent lymphocytosis cattle.
在来自感染 BLV 的持续性淋巴细胞增多牛的 B 细胞中,B 细胞受体向脂筏的易位受到抑制。
DOI:
10.1016/s0042-6822(03)00522-1
发表时间:
2003
期刊:
Virology
影响因子:
3.7
作者:
[Hamilton,ValerieT, Stone,DianaM, Cantor,GlennH]
通讯作者:
Cantor,GlennH
Bovine leukemia virus gp30 transmembrane (TM) protein is not tyrosine phosphorylated: examining potential interactions with host tyrosine-mediated signaling.
牛白血病病毒 gp30 跨膜 (TM) 蛋白未被酪氨酸磷酸化:检查与宿主酪氨酸介导的信号传导的潜在相互作用。
DOI:
10.1016/s0168-1702(02)00149-1
发表时间:
2002
期刊:
Virus research
影响因子:
5
作者:
[Hamilton,ValerieT, Stone,DianaM, Pritchard,SuzanneM, Cantor,GlennH]
通讯作者:
Cantor,GlennH
INTERACTIONS OF BLV GP30 WITH B CELL SIGNAL PATHWAYS
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批准号:2886116
-
项目类别:
-
资助金额:$7.19万
-
财政年份:1998
-
负责人:VALERIE T HAMILTON
-
依托单位:
INTERACTIONS OF BLV GP30 WITH B CELL SIGNAL PATHWAYS
-
批准号:2680029
-
项目类别:
-
资助金额:$6.96万
-
财政年份:1998
-
负责人:VALERIE T HAMILTON
-
依托单位:
海外基金