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https://doi.org/10.1155/1993/43482
Title: | Characterization of Thymic Nurse-Cell Lymphocytes, Using an Improved Procedure for Nurse-Cell Isolation | Authors: | Lahoud, M Vremec, D Boyd, R.L Shortman, K |
Keywords: | biological marker CD3 antigen CD4 antigen CD8 antigen animal article cell separation cytology female flow cytometry methodology mouse mouse strain phenotype physiology T lymphocyte T lymphocyte subpopulation thymus Animal Antigens, CD3 Antigens, CD4 Antigens, CD8 Biological Markers CD4-Positive T-Lymphocytes Cell Separation Female Flow Cytometry Mice Mice, Inbred CBA Phenotype Support, Non-U.S. Gov't T-Lymphocyte Subsets T-Lymphocytes Thymus Gland |
Issue Date: | 1993 | Citation: | Lahoud, M, Vremec, D, Boyd, R.L, Shortman, K (1993). Characterization of Thymic Nurse-Cell Lymphocytes, Using an Improved Procedure for Nurse-Cell Isolation. Developmental Immunology 3 (2) : 103-112. ScholarBank@NUS Repository. https://doi.org/10.1155/1993/43482 | Rights: | Attribution 4.0 International | Abstract: | Thymic nurse cells (TNC), multicellular complexes consisting of lymphoid cells enclosed within cortical epithelial cells, were isolated from mouse thymus by a modified procedure allowing immunofluorescent labeling and flow cytometric analysis of their lymphoid contents (TNC-L). Collagenase was the only protease used for tissue digestion, to ensure that surface antigen markers remained intact. Zonal unit-gravity elutriation was used to enrich the TNC on the basis of their high sedimentation rate, followed by immunomagnetic bead depletion to remove residual mononuclear cell contaminants and a density separation to remove debris. The TNC-L were then released from inside TNC by a short period of culture. The measured contamination of TNC-L with exogenous thymocytes was around 0.5%. Three-color immunofluorescent labeling revealed that TNC-L included, as well as a majority of immature CD4+8+3low thymocytes, about 12% of apparently mature CD4+8-3high and CD4~8+3high thymocytes. TNC are located in the cortex, where mature cells are rare; the occurrence of mature phenotype cells within these structures suggests that they represent a microenvironment for the selection and generation of mature T cells. © 1993, Harwood Academic Publishers GmbH. | Source Title: | Developmental Immunology | URI: | https://scholarbank.nus.edu.sg/handle/10635/181148 | ISSN: | 10446672 | DOI: | 10.1155/1993/43482 | Rights: | Attribution 4.0 International |
Appears in Collections: | Elements Staff Publications |
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