GAMMA GLUTAMYL TRANSPEPTIDASE & LYMPHOCYTE ACTIVATION
GAMMA GLUTAMYL TRANSPEPTIDASE & LYMPHOCYTE ACTIVATION
批准号:
6510801
负责人:
DAVID R KARP
金额:
$24.14万
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-03-15 至 2004-02-28
关键词:
CD antigens T lymphocyte apoptosis cell cycle cell migration cytokine enzyme activity enzyme induction /repression flow cytometry genetically modified animals glutamyltransferase glutathione immunologic memory laboratory mouse leukocyte activation /transformation messenger RNA oxidative stress protein isoforms protein tyrosine phosphatase surface antigens
中文摘要
描述:(改编自申请人的摘要)- T
英文摘要
DESCRIPTION: (Adapted from the applicant's abstract) - The interaction of T
cells with antigen (Ag) leads to the generation of effector and memory cells.
Memory cells have characteristic cell surface marker profiles, and are able to
rapidly respond to recall antigens. CD4+ memory cells accumulate in the
periphery during aging, following chronic stimulation, and in autoimmune
diseases like rheumatoid arthritis (RA). Recently, the applicant has found that
the ecto-enzyme gamma glutamyl transpeptidase (GGT) is up-regulated upon T cell
activation, and is highly expressed by memory T cells. High levels of GGT are
also found in T cells with the capacity to cross endothelial barriers, and on
resting peripheral T cells in patients with RA. The role of this enzyme in
lymphocyte biology is unclear, but it may be important in maintenance of
intracellular re-dox potential and signaling events. The aims of this
application are to 1) determine whether GGT is a better marker of memory T
cells than previously described surface Ags; 2) determine the role of GGT in T
cell biology; and 3) determine the role of GGT in transendothelial migration of
peripheral blood T cells. Experiments proposed include flow cytometric
analysis, functional responses of GGT expressing cells to determine if these
cells indeed have memory function; and using various strategies to disrupt
enzymatic activity, the applicant will test the effect of GGT on activation,
growth, and apoptosis. These experiments will provide a thorough description of
GGT function in lymphocytes, and should be useful in expanding our knowledge
about the memory T cell compartment. GGT also may be a potential target in
future immunotherapy strategies.
期刊论文(5)
专著(0)
科研奖励(0)
会议论文
The ectoenzyme gamma-glutamyl transpeptidase regulates antiproliferative effects of S-nitrosoglutathione on human T and B lymphocytes.
胞外酶 γ-谷氨酰转肽酶调节 S-亚硝基谷胱甘肽对人 T 和 B 淋巴细胞的抗增殖作用。
DOI:
--
发表时间:
1999
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
[Henson,SE, Nichols,TC, Holers,VM, Karp,DR]
通讯作者:
Karp,DR
Reanalysis of the involvement of gamma-glutamyl transpeptidase in the cell activation process.
重新分析γ-谷氨酰转肽酶在细胞活化过程中的参与。
DOI:
10.1016/s0014-5793(01)03057-5
发表时间:
2001
期刊:
FEBS letters
影响因子:
3.5
作者:
[Antczak,C, Karp,DR, London,RE, Bauvois,B]
通讯作者:
Bauvois,B
Study of Anti-Malarials in Incomplete Lupus Erythematosus (SMILE)
-
批准号:10348096
-
项目类别:
-
资助金额:$93.48万
-
财政年份:2017
-
负责人:DAVID R KARP
-
依托单位:
Study of Anti-Malarials in Incomplete Lupus Erythematosus (SMILE)
-
批准号:9888967
-
项目类别:
-
资助金额:$131.51万
-
财政年份:2017
-
负责人:DAVID R KARP
-
依托单位:
Hydroxychloroquine Treatment for Prevention of Systemic Lupus Erythematosus
-
批准号:8813684
-
项目类别:
-
资助金额:$36.17万
-
财政年份:2015
-
负责人:DAVID R KARP
-
依托单位:
Hydroxychloroquine Treatment for Prevention of Systemic Lupus Erythematosus
-
批准号:8996136
-
项目类别:
-
资助金额:$32.1万
-
财政年份:2015
-
负责人:DAVID R KARP
-
依托单位:
Clinical Resource Core
-
批准号:7941913
-
项目类别:
-
资助金额:$14.31万
-
财政年份:2009
-
负责人:DAVID R KARP
-
依托单位:
High Throughput Screening of the Autoimmune Epitome
-
批准号:7937043
-
项目类别:
-
资助金额:$48.56万
-
财政年份:2009
-
负责人:DAVID R KARP
-
依托单位:
High Throughput Screening of the Autoimmune Epitome
-
批准号:7842417
-
项目类别:
-
资助金额:$48.88万
-
财政年份:2009
-
负责人:DAVID R KARP
-
依托单位:
Clinical Resource Core
-
批准号:7673591
-
项目类别:
-
资助金额:$17.48万
-
财政年份:2008
-
负责人:DAVID R KARP
-
依托单位:
Clinical Resource Core
-
批准号:7345037
-
项目类别:
-
资助金额:$12.99万
-
财政年份:2007
-
负责人:DAVID R KARP
-
依托单位:
NIAMS: CORT - Genetic Dissection of SLE--From Mouse to Man
-
批准号:8128710
-
项目类别:
-
资助金额:$147.08万
-
财政年份:2007
-
负责人:DAVID R KARP
-
依托单位:
The Function of Human AIM in Rheumatic Disease
-
批准号:6948562
-
项目类别:
-
资助金额:$15.6万
-
财政年份:2004
-
负责人:DAVID R KARP
-
依托单位:
The Function of Human AIM in Rheumatic Disease
-
批准号:6839655
-
项目类别:
-
资助金额:$15.6万
-
财政年份:2004
-
负责人:DAVID R KARP
-
依托单位:
Oxidative Stress and Functional Lymphocyte Development
-
批准号:7034607
-
项目类别:
-
资助金额:$26.66万
-
财政年份:2002
-
负责人:DAVID R KARP
-
依托单位:
Oxidative Stress and Functional Lymphocyte Development
-
批准号:6620515
-
项目类别:
-
资助金额:$27.3万
-
财政年份:2002
-
负责人:DAVID R KARP
-
依托单位:
Oxidative Stress and Functional Lymphocyte Development
-
批准号:6418469
-
项目类别:
-
资助金额:$27.3万
-
财政年份:2002
-
负责人:DAVID R KARP
-
依托单位:
Oxidative Stress and Functional Lymphocyte Development
-
批准号:6722919
-
项目类别:
-
资助金额:$27.3万
-
财政年份:2002
-
负责人:DAVID R KARP
-
依托单位:
Oxidative Stress and Functional Lymphocyte Development
-
批准号:6876546
-
项目类别:
-
资助金额:$27.3万
-
财政年份:2002
-
负责人:DAVID R KARP
-
依托单位:
CORE--PROTEIN AND MOLECULAR BIOLOGY FACILITY
-
批准号:6484673
-
项目类别:
-
资助金额:$24.75万
-
财政年份:2001
-
负责人:DAVID R KARP
-
依托单位:
CORE--PROTEIN AND MOLECULAR BIOLOGY FACILITY
-
批准号:6216430
-
项目类别:
-
资助金额:$17.9万
-
财政年份:2000
-
负责人:DAVID R KARP
-
依托单位:
CORE--PROTEIN AND MOLECULAR BIOLOGY FACILITY
-
批准号:6344602
-
项目类别:
-
资助金额:$17.9万
-
财政年份:2000
-
负责人:DAVID R KARP
-
依托单位:
海外基金