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Dynamics of Thymocyte-Stromal Cell Interactions Visualized by Two-Photon Microscopy
Thymocytes are selected to mature according to their ability to interact with self major histocompatibility complex (MHC)-peptide complexes displayed on the thymic stroma. Using two-photon microscopy, we performed real-time analysis of the cellular contacts made by developing thymocytes undergoing p...
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Published in: | Science (American Association for the Advancement of Science) 2002-06, Vol.296 (5574), p.1876-1880 |
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creator | Bousso, Philippe Bhakta, Nirav R. Lewis, Richard S. Robey, Ellen |
description | Thymocytes are selected to mature according to their ability to interact with self major histocompatibility complex (MHC)-peptide complexes displayed on the thymic stroma. Using two-photon microscopy, we performed real-time analysis of the cellular contacts made by developing thymocytes undergoing positive selection in a three-dimensional thymic organ culture. A large fraction of thymocytes within these cultures were highly motile. MHC recognition was found to increase the duration of thymocyte-stromal cell interactions and occurred as both long-lived cellular associations displaying stable cell-cell contacts and as shorter, highly dynamic contacts. Our results identify the diversity and dynamics of thymocyte interactions during positive selection. |
doi_str_mv | 10.1126/science.1070945 |
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Using two-photon microscopy, we performed real-time analysis of the cellular contacts made by developing thymocytes undergoing positive selection in a three-dimensional thymic organ culture. A large fraction of thymocytes within these cultures were highly motile. MHC recognition was found to increase the duration of thymocyte-stromal cell interactions and occurred as both long-lived cellular associations displaying stable cell-cell contacts and as shorter, highly dynamic contacts. Our results identify the diversity and dynamics of thymocyte interactions during positive selection.</description><identifier>ISSN: 0036-8075</identifier><identifier>EISSN: 1095-9203</identifier><identifier>DOI: 10.1126/science.1070945</identifier><identifier>PMID: 12052962</identifier><identifier>CODEN: SCIEAS</identifier><language>eng</language><publisher>Washington, DC: American Society for the Advancement of Science</publisher><subject>Analysis of the immune response. 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Using two-photon microscopy, we performed real-time analysis of the cellular contacts made by developing thymocytes undergoing positive selection in a three-dimensional thymic organ culture. A large fraction of thymocytes within these cultures were highly motile. MHC recognition was found to increase the duration of thymocyte-stromal cell interactions and occurred as both long-lived cellular associations displaying stable cell-cell contacts and as shorter, highly dynamic contacts. Our results identify the diversity and dynamics of thymocyte interactions during positive selection.</description><subject>Analysis of the immune response. 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Science)</jtitle><addtitle>Science</addtitle><date>2002-06-07</date><risdate>2002</risdate><volume>296</volume><issue>5574</issue><spage>1876</spage><epage>1880</epage><pages>1876-1880</pages><issn>0036-8075</issn><eissn>1095-9203</eissn><coden>SCIEAS</coden><abstract>Thymocytes are selected to mature according to their ability to interact with self major histocompatibility complex (MHC)-peptide complexes displayed on the thymic stroma. Using two-photon microscopy, we performed real-time analysis of the cellular contacts made by developing thymocytes undergoing positive selection in a three-dimensional thymic organ culture. A large fraction of thymocytes within these cultures were highly motile. MHC recognition was found to increase the duration of thymocyte-stromal cell interactions and occurred as both long-lived cellular associations displaying stable cell-cell contacts and as shorter, highly dynamic contacts. Our results identify the diversity and dynamics of thymocyte interactions during positive selection.</abstract><cop>Washington, DC</cop><pub>American Society for the Advancement of Science</pub><pmid>12052962</pmid><doi>10.1126/science.1070945</doi><tpages>5</tpages></addata></record> |
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ispartof | Science (American Association for the Advancement of Science), 2002-06, Vol.296 (5574), p.1876-1880 |
issn | 0036-8075 1095-9203 |
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subjects | Analysis of the immune response. Humoral and cellular immunity Animals Antigen Presentation Benzopyrans Biological and medical sciences CD8-Positive T-Lymphocytes - immunology Cell Aggregation Cell Communication Cell interactions Cell Movement Cell Size Cellular biology Coculture Techniques Endothelial cells Fluoresceins Fluorescent Dyes Fundamental and applied biological sciences. Psychology Fundamental immunology Genetic aspects Histocompatibility Antigens Class I - immunology Imaging Immunity Immunobiology Individualized Instruction Lasers Lymphatic system Lymphocytes Mice Mice, Inbred C57BL Mice, Transgenic Microscopy Microscopy - methods Naphthols Organ Culture Techniques Peptides Photons Positive selection Receptors, Antigen, T-Cell - immunology Rhodamines Signal Transduction Stromal cells Stromal Cells - immunology Stromal Cells - physiology Succinimides T cell antigen receptors T cells T lymphocytes T-Lymphocyte Subsets - immunology T-Lymphocytes - cytology T-Lymphocytes - immunology T-Lymphocytes - physiology Thymocytes Thymus Gland - cytology Thymus Gland - immunology Time Factors Topology |
title | Dynamics of Thymocyte-Stromal Cell Interactions Visualized by Two-Photon Microscopy |
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