Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

The thymic microenvironment involves complex cell interactions among different types of epithelial cells, macrophages, tissue histiocytes, and immature and maturing T cells. We describe the isolation of a subset of thymic epithelial cells by selective primary culture followed by cotransfection with a simian virus 40 replication-origin-defective mutant and pSV2neo plasmid. The cloned cells have the composite immunophenotype that is unique to thymic subcapsular epithelial cells, suggesting that they may provide a model system in vitro for analyzing the earliest steps in T-cell differentiation. This possibility is supported by the finding that these epithelial cells express LFA-3-associated binding sites for T cells, secrete a macrophage hemopoietic growth factor, and synergize with macrophages in the production of interleukin 1.

More information Original publication

DOI

10.1073/pnas.84.14.4999

Type

Journal article

Publication Date

1987-07-01T00:00:00+00:00

Volume

84

Pages

4999 - 5003

Total pages

4

Keywords

Antigens, Differentiation, T-Lymphocyte, Antigens, Surface, Cell Differentiation, Clone Cells, Colony-Stimulating Factors, Epithelial Cells, Epithelium, Hematopoietic Stem Cells, Humans, Interleukin-1, Lymphocyte Function-Associated Antigen-1, Macrophages, T-Lymphocytes, Thymus Gland