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THE ROLE OF T LYMPHOCYTE FACTORS IN HEMOPOIESIS

THE ROLE OF T LYMPHOCYTE FACTORS IN HEMOPOIESIS
T 淋巴细胞因子在造血中的作用
批准号:
3131933
负责人:
MICHAEL B PRYSTOWSKY
金额:
$9.83万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1985
资助国家:
美国
项目状态:
已结题
起止时间:
1985-04-01 至 1988-03-31

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项目成果

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中文摘要
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英文摘要
Inflammation is a complex host response that involves several biochemical pathways and all hemopoietic elements. T lymphocytes play an integral role in inflammatory responses by secreting soluble protein factors, lymphokines, that can regulate both the immunospecific and generalized aspects of the response. The first cells to arrive at a site of inflammation are neutrophilic granulocytes; macrophages usually appear several hours after granulocytes. Cloned T lymphocytes are a potent source of factors that affect hemopoiesis. The major hemopoietically active factor that is secreted by T lymphocytes is a granulocyte-macrophage colony-stimulating factor (GM-CSF). During an inflammatory response this GM-CSF may act distally on bone marrow cells to increase the number of responding granulocytes and macrophages. A major goal of this project is to purify to homogeneity the T lymphocyte GM-CSF. A highly enriched preparation of GM-CSF has been obtained with the use of high-pressure liquid chromatography. When serum free T lymphocyte-conditioned medium is used as a starting material, the GM-CSF will be purified to homogeneity. Another aim of this project is to determine the nature of the interaction between GM-CSF, IL3 (which is also produced by T lymphocytes), and erythropoietin. It has been shown already tha IL3 potentiates the effects of erythropoietin. However, T lymphocytes secrete about 10-100-fold more GM-CSF than IL3; the molecular basis for the net effect on bone marrow cells when all three factors are present in physiological or pathophysiological (i.e. during inflammation) concentrations is unknown but testable with pure factors. In addition, homogeneous GM-CSF will be subjected to mild proteolysis in an attempt to produce biologically active peptides to determine the minimal structural requirements that are necessary for biological activity. A longterm goal of this project will be to synthesize chemically bioactive peptides and structural analogs that can be used as either stimulatory or inhibitory effectors of hemopoiesis. These studies will further our understanding of the role that T lymphocytes play in regulating hemopoiesis.
期刊论文(4)
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会议论文
Cloned T-cell proliferation and synthesis of specific proteins are inhibited by quinine.
奎宁可抑制克隆 T 细胞的增殖和特定蛋白质的合成。
DOI: 10.1073/pnas.83.13.4739
发表时间: 1986
期刊: Proceedings of the National Academy of Sciences of the United States of America
影响因子: 11.1
作者: [Sabath,DE, Monos,DS, Lee,SC, Deutsch,C, Prystowsky,MB]
通讯作者: Prystowsky,MB
Cyclin mRNA and protein expression in recombinant interleukin 2-stimulated cloned murine T lymphocytes.
重组白细胞介素 2 刺激的克隆鼠 T 淋巴细胞中细胞周期蛋白 mRNA 和蛋白的表达。
DOI: 10.1002/jcb.240380306
发表时间: 1988
期刊: Journal of cellular biochemistry
影响因子: 4
作者: [Shipman,PM, Sabath,DE, Fischer,AH, Comber,PG, Sullivan,K, Tan,EM, Prystowsky,MB]
通讯作者: Prystowsky,MB
Partial Characterization ofaFibroblast-Stimu lating Factor Produced byCloned Murine TLymphocytes
克隆鼠T淋巴细胞产生的成纤维细胞刺激因子的部分表征
DOI: 10.1097/00007890-199912150-00027
发表时间: 1988
期刊: Transplantation
影响因子: 6.2
作者: [J. Monroe, A. I. Michael, G. Johnson, S. Phillips, B. Prystowsky]
通讯作者: B. Prystowsky
Myeloperoxidase and oncogene expression in GM-CSF induced bone marrow differentiation.
GM-CSF 中的髓过氧化物酶和癌基因表达诱导骨髓分化。
DOI: --
发表时间: 1988
期刊: Oncogene
影响因子: 8
作者: [Jaffe,BD, Sabath,DE, Johnson,GD, Moscinski,LC, Johnson,KR, Rovera,G, Nauseef,WM, Prystowsky,MB]
通讯作者: Prystowsky,MB
Proteomic analysis of head & neck squamous cell cancer
Proteomic analysis of head & neck squamous cell cancer
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