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Expansion of an unusual population of Gr-1+CD3int cells in the lymph nodes and other peripheral organs of mice carrying the lpr gene.

作者信息

Honda S, Takeda K, Narita J, Koya T, Kawamura T, Kuwano Y, Watanabe H, Arakawa M, Abo T

机构信息

Second Department of Internal Medicine, Niigata University School of Medicine, Japan.

出版信息

Cell Immunol. 1997 May 1;177(2):144-53. doi: 10.1006/cimm.1997.1104.

DOI:10.1006/cimm.1997.1104
PMID:9178641
Abstract

Granulocytes and extrathymic T cells are often activated simultaneously, but they are absolutely separate populations in normal mice. However, some abnormal extrathymic T cells (i.e., CD3int cells) seen in mice carrying the lpr gene were found to express a granulocyte marker, Gr-1. Such mice include MRL-lpr/lpr mice and SCG mice. In parallel with an age-associated increase of IL-2Rbeta(low)CD3int cells which contained double-negative CD4-8- and B220+CD2- cells, Gr-1+CD3int cells increased in number in the lymph nodes and other peripheral organs. In addition to a major population of IL-2Rbeta(low)CD3int cells, there is a small population of IL-2Rbeta(high)CD3int cells which produce normal Fas mRNA and Fas molecule from the lpr gene. It was found that both IL-2Rbeta(low)CD3int and IL-2Rbeta(high)CD3int cell populations contained Gr-1+ cells. IL-2Rbeta(high)CD3int cells tended to contain a higher proportion of Gr-1+ cells than did IL-2Rbeta(low)CD3int cells. More interestingly, Gr-1+CD3int cells expressed a considerable level of mRNA of the mG-CSF receptor, similar to granulocytes. The present study thus yielded further information on an unusual property of abnormally expanding CD3int cells in mice carrying the lpr gene.

摘要

相似文献

1
Expansion of an unusual population of Gr-1+CD3int cells in the lymph nodes and other peripheral organs of mice carrying the lpr gene.
Cell Immunol. 1997 May 1;177(2):144-53. doi: 10.1006/cimm.1997.1104.
2
Existence of a small population of IL-2R beta hi TCRint cells in SCG and MRL-lpr/lpr mice which produce normal Fas mRNA and Fas molecules from the lpr gene.在颈上神经节(SCG)和MRL-lpr/lpr小鼠中存在一小群IL-2Rβ高表达TCR中等表达的细胞,这些细胞从lpr基因产生正常的Fas mRNA和Fas分子。
Eur J Immunol. 1996 Jul;26(7):1409-16. doi: 10.1002/eji.1830260702.
3
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。
J Immunol. 1995 May 15;154(10):4986-95.
4
Characterization of intermediate T-cell receptor cells expanding in the liver, thymus and other organs in autoimmune lpr mice: parallel analysis with their normal counterparts.自身免疫性lpr小鼠肝脏、胸腺及其他器官中扩增的中间型T细胞受体细胞的特征:与其正常对应细胞的平行分析
Immunology. 1995 Apr;84(4):601-8.
5
Intermediate TCR cells in mouse lung: their effector function to induce pneumonitis in mice with autoimmune-like graft-versus-host disease.小鼠肺中的中间型TCR细胞:它们在自身免疫样移植物抗宿主病小鼠中诱导肺炎的效应功能。
J Immunol. 1997 Jun 15;158(12):5805-14.
6
The proliferative in vivo activities of lpr double-negative T cells and the primary role of p59fyn in their activation and expansion.lpr双阴性T细胞的体内增殖活性以及p59fyn在其激活和扩增中的主要作用。
J Immunol. 1997 Sep 1;159(5):2265-73.
7
Autoreactivity accelerates the development of autoimmunity and lymphoproliferation in MRL/Mp-lpr/lpr mice.自身反应性加速了MRL/Mp-lpr/lpr小鼠自身免疫和淋巴细胞增殖的发展。
J Immunol. 1987 Aug 1;139(3):734-42.
8
Expression of the J11d marker on peripheral T lymphocytes of MRL-lpr/lpr mice.J11d标记物在MRL-lpr/lpr小鼠外周T淋巴细胞上的表达。
J Immunol. 1988 Aug 15;141(4):1120-5.
9
CD2-CD4-CD8- lymph node T lymphocytes in MRL lpr/lpr mice are derived from a CD2+CD4+CD8+ thymic precursor.MRL lpr/lpr小鼠中CD2-CD4-CD8-淋巴结T淋巴细胞来源于CD2+CD4+CD8+胸腺前体细胞。
J Immunol. 1993 Jul 15;151(2):1086-96.
10
Age-dependent variation in the proportion and number of intestinal lymphocyte subsets, especially natural killer T cells, double-positive CD4+ CD8+ cells and B220+ T cells, in mice.小鼠肠道淋巴细胞亚群(尤其是自然杀伤T细胞、双阳性CD4⁺CD8⁺细胞和B220⁺T细胞)比例和数量的年龄依赖性变化。
Immunology. 2004 Nov;113(3):371-7. doi: 10.1111/j.1365-2567.2004.01961.x.

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