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MRL-lpr/lpr小鼠中一种新型的CD45RA⁺CD4⁺短暂性胸腺亚群:其与非增殖性CD4⁻CD8⁻CD45RA⁺肿瘤细胞的关系。

A novel CD45RA+CD4+ transient thymic subpopulation in MRL-lpr/lpr mice: its relation to non-proliferating CD4-CD8-CD45RA+ tumor cells.

作者信息

Ezine S, Lucas B, Vicari A, Dautigny N, Vasseur F, Penit C

机构信息

U345 INSERM, CHU Necker-Enfants Malades, Paris, France.

出版信息

Int Immunol. 1993 Jan;5(1):89-96. doi: 10.1093/intimm/5.1.89.

DOI:10.1093/intimm/5.1.89
PMID:8443124
Abstract

MRL-lpr/lpr mice have hypertrophied lymph nodes comprising CD4-CD8- T cells. In addition, they contain CD4+CD8- T cells co-expressing the CD45RA marker. The correlation between these two subpopulations has been difficult to assess. We analyzed the expression of CD45RA (with the RA3-2C2 antibody) in various thymic and peripheral T cell subsets, using three-color immunofluorescence. We showed that in lpr mice (i) a transient CD4+CD8- thymic subset co-expresses CD45RA during the course of the disease, and (ii) thymic as well as peripheral CD4-CD8- and CD4+CD8- T cells brightly express CD45RA; furthermore (iii) in the lymph nodes, during lymphadenopathy, CD4+CD8-CD45RA+ T cells show a broad range of the CD4 fluorescence intensity, and (iv) the increase in MHC class II expression is restricted to CD45RA-T cells of the thymus and lymph nodes of lpr mice. Taken together, these data suggest that the CD4+CD8-CD45RA+ population might generate the CD4-CD8- tumor cells. In addition, using the bromodeoxyuridine labeling technique, we demonstrate that these cells are not the result of increased proliferation.

摘要

MRL-lpr/lpr小鼠有肥大的淋巴结,其中包含CD4-CD8-T细胞。此外,它们还含有共表达CD45RA标志物的CD4+CD8-T细胞。这两个亚群之间的相关性一直难以评估。我们使用三色免疫荧光分析了各种胸腺和外周T细胞亚群中CD45RA(用RA3-2C2抗体)的表达。我们发现,在lpr小鼠中:(i)在疾病过程中,一个短暂的CD4+CD8-胸腺亚群共表达CD45RA;(ii)胸腺以及外周的CD4-CD8-和CD4+CD8-T细胞强烈表达CD45RA;此外,(iii)在淋巴结肿大期间,淋巴结中的CD4+CD8-CD45RA+T细胞显示出广泛的CD4荧光强度范围;(iv)MHC II类表达的增加仅限于lpr小鼠胸腺和淋巴结中的CD45RA-T细胞。综上所述,这些数据表明CD4+CD8-CD45RA+群体可能产生CD4-CD8-肿瘤细胞。此外,使用溴脱氧尿苷标记技术,我们证明这些细胞不是增殖增加的结果。

相似文献

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A novel CD45RA+CD4+ transient thymic subpopulation in MRL-lpr/lpr mice: its relation to non-proliferating CD4-CD8-CD45RA+ tumor cells.MRL-lpr/lpr小鼠中一种新型的CD45RA⁺CD4⁺短暂性胸腺亚群:其与非增殖性CD4⁻CD8⁻CD45RA⁺肿瘤细胞的关系。
Int Immunol. 1993 Jan;5(1):89-96. doi: 10.1093/intimm/5.1.89.
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Origin of CD4-CD8-B220+ T cells in MRL-lpr/lpr mice. Clues from a T cell receptor beta transgenic mouse.MRL-lpr/lpr小鼠中CD4-CD8-B220+ T细胞的起源。来自T细胞受体β转基因小鼠的线索。
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CD45RA antibodies split the CD3bright T cell subset.CD45RA抗体可将CD3bright T细胞亚群分开。
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Transgenic rearranged T cell receptor gene inhibits lymphadenopathy and accumulation of CD4-CD8-B220+ T cells in lpr/lpr mice.转基因重排的T细胞受体基因可抑制lpr/lpr小鼠的淋巴结病及CD4-CD8-B220+ T细胞的积聚。
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In CD8+ T cell-deficient lpr/lpr mice, CD4+B220+ and CD4+B220- T cells replace B220+ double-negative T cells as the predominant populations in enlarged lymph nodes.在CD8 + T细胞缺陷的lpr/lpr小鼠中,CD4 + B220 +和CD4 + B220 - T细胞取代B220 +双阴性T细胞,成为肿大淋巴结中的主要细胞群体。
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