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GORDON CONFERENCE--FIBRONECTIN AND MACROMOLECULES

GORDON CONFERENCE--FIBRONECTIN AND MACROMOLECULES
戈登会议--纤连蛋白和大分子
批准号:
3435740
负责人:
Mark HOWARD Ginsberg
金额:
$1.2万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1993
资助国家:
美国
项目状态:
已结题
起止时间:
1993-02-01 至 1994-01-31

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中文摘要
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英文摘要
The paradigm of an extracellular adhesin, fibronectin, interacting with a transmembrane receptor has proven applicable to a number of adhesion systems. There are several other extracellular glycoproteins with biological properties like fibronectin, laminin, thrombospondin, von Willebrand factor, fibrinogen/fibrin, vitronectin, and cytotactin/tenascin/hexabrachion. The primary structures of each of these proteins are determined and three-dimensional structures are in progress for some. This will open up new possibilities for studies of function. In parallel has come the realization that the transmembrane receptor for fibronectin is only one member of the integrin family of functionally related, homologous, cell adhesion receptors. Fibronectin and related macromolecules are involved in many basic functions of cells, including cell adhesion, determination of cell shape and differentiation, cell migration, cytoskeletal organization, and organization of extracellular matrix. Thus, fibronectin and the molecules with which it interacts are important in embryogenesis, connective tissue organization, hemostasis, thrombosis, wound healing, development of immunity, hematopoiesis, malignant transformation, and tumor metastasis. The challenges to the field over the next several years are to comprehend and organize the large amount of new structural information and design experiments based upon it; learn the relative biological importance of the several seemingly redundant adhesion systems; and apply the new insights to the treatment of human diseases. The 1993 Gordon Research Conference will serve as a valuable forum to present and discuss new information, identify problem areas, and plan new approaches.
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Cellular Mechanisms of Inflammation, Hemostasis, and Thrombosis
Cellular Mechanisms of Inflammation, Hemostasis, and Thrombosis
Direct Rap1-talin interaction in platelets, leukocytes, and endothelial cells
Core B - Ginsberg-ADMINISTRATIVE CORE
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