Massive and destructive T cell response to homeostatic cue in CD24-deficient lymphopenic hosts
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- Ou Li
- 1Division of Cancer Immunology, Department of Pathology, The Ohio State University Medical Center, Columbus, OH 43210
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- Xing Chang
- 1Division of Cancer Immunology, Department of Pathology, The Ohio State University Medical Center, Columbus, OH 43210
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- Huiming Zhang
- 1Division of Cancer Immunology, Department of Pathology, The Ohio State University Medical Center, Columbus, OH 43210
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- Ergun Kocak
- 1Division of Cancer Immunology, Department of Pathology, The Ohio State University Medical Center, Columbus, OH 43210
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- Cheng Ding
- 1Division of Cancer Immunology, Department of Pathology, The Ohio State University Medical Center, Columbus, OH 43210
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- Pan Zheng
- 1Division of Cancer Immunology, Department of Pathology, The Ohio State University Medical Center, Columbus, OH 43210
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- Yang Liu
- 1Division of Cancer Immunology, Department of Pathology, The Ohio State University Medical Center, Columbus, OH 43210
書誌事項
- 公開日
- 2006-06-12
- DOI
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- 10.1084/jem.20052293
- 公開者
- Rockefeller University Press
この論文をさがす
説明
<jats:p>In response to a lymphopenic cue, T lymphocytes undergo a slow-paced homeostatic proliferation in an attempt to restore T cell cellularity. The molecular interaction that maintains the pace of homeostatic proliferation is unknown. In this study, we report that in lymphopenic CD24-deficient mice, T cells launch a massive proliferation that results in the rapid death of the recipient mice. The dividing T cells have phenotypes similar to those activated by cognate antigens. The rapid homeostatic proliferation is caused by a lack of CD24 on dendritic cells (DCs). Interestingly, although CD24 expression in T cells is required for optimal homeostatic proliferation in the wild-type (WT) host, mice lacking CD24 on all cell types still mount higher homeostatic proliferation than the WT mice. Thus, a lack of CD24 in the non–T host cells bypassed the requirement for T cell expression of CD24 in homeostatic proliferation in the WT host. Our data demonstrate that CD24 expressed on the DCs limits T cell response to homeostatic cue and prevents fatal damage associated with uncontrolled homeostatic proliferation.</jats:p>
収録刊行物
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- The Journal of Experimental Medicine
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The Journal of Experimental Medicine 203 (7), 1713-1720, 2006-06-12
Rockefeller University Press
