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T细胞谱系干细胞的有限稀释分析。

Limiting dilution analysis of the stem cells for T cell lineage.

作者信息

Katsura Y, Kina T, Amagai T, Tsubata T, Hirayoshi K, Takaoki Y, Sado T, Nishikawa S I

出版信息

J Immunol. 1986 Oct 15;137(8):2434-9.

PMID:3489764
Abstract

Stem cell activities of bone marrow, spleen, thymus, and fetal liver cells for T cell lineage were studied comparatively by transferring the cells from these organs through i.v. or intrathymus (i.t.) route into right leg- and tail-shielded (L-T-shielded) and 900 R-irradiated recipient mice, which were able to survive without supplying hemopoietic stem cells. Cells from B10.Thy-1.1 (H-2b, Thy-1.1) mice were serially diluted and were transferred into L-T-shielded and irradiated C57BL/6 (H-2b, Thy-1.2) mice, and 21 days later the thymus cells of recipient mice were assayed for Thy-1.1+ cells by flow cytofluorometry. The percentage of recipient mice possessing donor-type T cells was plotted against the number of cells transferred, and the stem cell activity in each cell source was expressed as the 50% positive value, the number of donor cells required for generating donor-type T cells in the thymuses of 50% of recipient mice. In i.v. transfer experiments, the activity of bone marrow cells was similar to that of fetal liver cells, and about 100 times and nearly 1000 times higher than those of spleen cells and thymus cells, respectively. In i.t. transfer experiments, the number of cells required for generating donor-type T cells was much lower than that in i.v. transfer experiments, although the ratio in 50% positive values between i.v. and i.t. transfers differed among cell sources. In i.t. transfers, the 50% positive value of bone marrow cells was five times, 400 times, and 500 times higher than that of fetal liver cells, spleen cells, and thymus cells, respectively. Our previous finding that stem cells are enriched in the spleens of mice which were whole body-irradiated and marrow-reconstituted 7 days earlier was confirmed also by the present limiting dilution assay carried out in i.v. as well as i.t. transfers.

摘要

通过将来自这些器官的细胞经静脉内(i.v.)或经胸腺内(i.t.)途径注入右下肢和尾部屏蔽(L-T屏蔽)且经900拉德照射的受体小鼠体内,对骨髓、脾脏、胸腺和胎肝细胞在T细胞谱系方面的干细胞活性进行了比较研究,这些受体小鼠在不供应造血干细胞的情况下也能够存活。将来自B10.Thy-1.1(H-2b,Thy-1.1)小鼠的细胞进行连续稀释,并注入L-T屏蔽且经照射的C57BL/6(H-2b,Thy-1.2)小鼠体内,21天后通过流式细胞荧光术检测受体小鼠胸腺细胞中的Thy-1.1+细胞。将拥有供体型T细胞的受体小鼠的百分比与转移的细胞数量作图,每种细胞来源的干细胞活性以50%阳性值表示,即50%的受体小鼠胸腺中产生供体型T细胞所需的供体细胞数量。在静脉内转移实验中,骨髓细胞的活性与胎肝细胞相似,分别比脾细胞和胸腺细胞高约100倍和近1000倍。在经胸腺内转移实验中,产生供体型T细胞所需的细胞数量比静脉内转移实验中的要低得多,尽管静脉内和经胸腺内转移之间50%阳性值的比例在不同细胞来源中有所不同。在经胸腺内转移中,骨髓细胞的50%阳性值分别比胎肝细胞、脾细胞和胸腺细胞高5倍、400倍和500倍。我们之前的发现,即干细胞在7天前接受全身照射并进行骨髓重建的小鼠脾脏中富集,在本次静脉内以及经胸腺内转移的有限稀释实验中也得到了证实。

相似文献

1
Limiting dilution analysis of the stem cells for T cell lineage.T细胞谱系干细胞的有限稀释分析。
J Immunol. 1986 Oct 15;137(8):2434-9.
2
Two subpopulations of stem cells for T cell lineage.T细胞谱系干细胞的两个亚群。
J Immunol. 1985 Nov;135(5):3021-7.
3
Quantification of the progenitors for thymic T cells in various organs.不同器官中胸腺T细胞祖细胞的定量分析。
Eur J Immunol. 1988 Jun;18(6):889-95. doi: 10.1002/eji.1830180609.
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A role for the thymic epithelium in the selection of pre-T cells from murine bone marrow.胸腺上皮在从小鼠骨髓中选择前T细胞过程中的作用。
J Immunol. 1989 Aug 15;143(4):1077-86.
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Functional differentiation and repertoire diversification of T cells derived from single progenitor cells.源自单个祖细胞的T细胞的功能分化和谱系多样化。
Eur J Immunol. 1988 Jun;18(6):897-903. doi: 10.1002/eji.1830180610.
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Intrathymic T cell differentiation in radiation bone marrow chimeras and its role in T cell emigration to the spleen. An immunohistochemical study.辐射骨髓嵌合体中胸腺内T细胞分化及其在T细胞迁移至脾脏中的作用。一项免疫组织化学研究。
J Immunol. 1985 Jun;134(6):3615-24.
7
Dysfunction of irradiated thymus for the development of helper T cells.受照射的胸腺功能障碍对辅助性T细胞发育的影响。
J Immunol. 1987 Jul 15;139(2):358-64.
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[Absence of a stimulating effect of T-lymphocytes on the colony-forming activity of splenic hematopoietic stem cells].[T淋巴细胞对脾造血干细胞集落形成活性无刺激作用]
Biull Eksp Biol Med. 1982 Dec;94(12):85-7.
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Hemopoietic progenitors in the murine fetal liver capable of rapidly generating T cells.小鼠胎肝中能够快速产生T细胞的造血祖细胞。
J Immunol. 1997 Apr 1;158(7):3118-24.
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Emergence of T, B, and myeloid lineage-committed as well as multipotent hemopoietic progenitors in the aorta-gonad-mesonephros region of day 10 fetuses of the mouse.在小鼠胚胎第10天的主动脉-性腺-中肾区域出现T、B和髓系定向以及多能造血祖细胞。
J Immunol. 1999 Nov 1;163(9):4788-95.

引用本文的文献

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Enhancement of activation-induced cell death by fibronectin in murine CD4+ CD8+ thymocytes.纤连蛋白增强小鼠CD4⁺CD8⁺胸腺细胞中活化诱导的细胞死亡
Immunology. 1998 Dec;95(4):553-8. doi: 10.1046/j.1365-2567.1998.00636.x.
2
Differentiation of CD3-4-8- human fetal thymocytes in vivo: characterization of a CD3-4+8- intermediate.体内CD3 - 4 - 8 - 人胎儿胸腺细胞的分化:CD3 - 4 + 8 - 中间阶段的特征
J Exp Med. 1993 Jul 1;178(1):265-77. doi: 10.1084/jem.178.1.265.
3
Phenotypic and genotypic characteristics of the human prothymocyte.
人类前胸腺细胞的表型和基因型特征
Immunol Res. 1987;6(4):250-62. doi: 10.1007/BF02935519.
4
Two rare populations of mouse Thy-1lo bone marrow cells repopulate the thymus.两类罕见的小鼠Thy-1lo骨髓细胞群可使胸腺重新形成细胞群体。
J Exp Med. 1988 May 1;167(5):1671-83. doi: 10.1084/jem.167.5.1671.
5
Antibody which defines a subset of bone marrow cells that can migrate to thymus.一种能定义可迁移至胸腺的骨髓细胞亚群的抗体。
Immunology. 1989 Sep;68(1):59-65.