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不同器官中胸腺T细胞祖细胞的定量分析。

Quantification of the progenitors for thymic T cells in various organs.

作者信息

Katsura Y, Kina T, Takaoki Y, Nishikawa S

机构信息

Chest Disease Research Institute, Kyoto University, Japan.

出版信息

Eur J Immunol. 1988 Jun;18(6):889-95. doi: 10.1002/eji.1830180609.

Abstract

Partial characterization and frequency determination of the progenitors for thymic T cells in various organs were made by transferring cells directly into the thymus (intrathymically, i.t.). B10. Thy-1.1 (H-2b, Thy-1.1) mice were used as the donor, and C57BL/6 (H-2b, Thy-1.2) mice that had been whole body irradiated with 800 rads and reconstituted with 10(7) syngeneic (B6) bone marrow (BM) cells were used as the recipient. BM cells, spleen cells and thymus cells from young adults and fetal liver cells (day 14 of gestation) were treated with anti-Thy-1.1 antibody plus complement, and transferred i.t. The generation of Thy-1.1+ donor type cells in the recipient's thymus was investigated by using flow cytometry. From the time course of generation, it was shown that the progenitor cells in the thymus were distinct from those in other organs. After the transfer of thymic non-T cells, donor-type cells began to generate on the 4th day, the proportion of donor-type T cells increased quickly thereafter, and the progenitors in this organ ceased to produce T cells by day 21. On the other hand, a latent period of about 10 days was required for progenitor cells in the BM, spleen or fetal liver to generate T cells, and T cell producing-activity of the progenitor cells in these organs lasted as long as 7 weeks. The frequency of progenitor cells was analyzed by transferring serial dilutions of anti-Thy-1.1 plus complement-treated cells i.t. and investigating the generation of donor-type T cells in the recipient's thymus on day 11 in the case transferred with thymic cells and on day 21 in other cases. The proportion of negative recipients which did not contain detectable levels of donor-type cells was plotted on a logarithmic scale against the number of cells transferred on a linear scale. The progenitor cell frequencies in BM, spleen, thymus and fetal liver were estimated to be 12.5 x 10(-5), 6.25 x 10(-5), 0.22 x 10(-5) and 0.14 x 10(-5), respectively. The reliability of the frequency determination was supported by the finding that when a limited number (10(3)) of a 1:1 mixture of BM cells from two mutually identifiable donors was transferred i.t., most of the recipients were negative for donor-type T cells and 3 out of 4 positive recipients were seeded by progenitor cells of a single donor.

摘要

通过将细胞直接注入胸腺(经胸腺内,i.t.),对不同器官中胸腺T细胞祖细胞进行了部分特性鉴定和频率测定。以B10.Thy-1.1(H-2b,Thy-1.1)小鼠作为供体,将经800拉德全身照射并用10⁷同基因(B6)骨髓(BM)细胞重建的C57BL/6(H-2b,Thy-1.2)小鼠作为受体。来自年轻成年小鼠的BM细胞、脾细胞和胸腺细胞以及胎肝细胞(妊娠第14天)用抗Thy-1.1抗体加补体处理后经胸腺内注入。通过流式细胞术研究受体胸腺中Thy-1.1⁺供体型细胞的产生。从产生的时间进程来看,结果表明胸腺中的祖细胞与其他器官中的祖细胞不同。注入胸腺非T细胞后,供体型细胞在第4天开始产生,此后供体型T细胞的比例迅速增加,该器官中的祖细胞在第21天时停止产生T细胞。另一方面,BM、脾脏或胎肝中的祖细胞产生T细胞需要约10天的潜伏期,这些器官中祖细胞的T细胞产生活性可持续长达7周。通过经胸腺内注入抗Thy-1.1加补体处理细胞的系列稀释液,并在注入胸腺细胞的情况下于第11天以及在其他情况下于第21天研究受体胸腺中供体型T细胞的产生,对祖细胞频率进行了分析。将不含可检测水平供体型细胞的阴性受体比例以对数标度绘制,而将注入细胞的数量以线性标度绘制。估计BM、脾脏、胸腺和胎肝中的祖细胞频率分别为12.5×10⁻⁵、6.25×10⁻⁵、0.22×10⁻⁵和0.14×10⁻⁵。当经胸腺内注入有限数量(10³)的来自两个可相互识别供体的BM细胞的1:1混合物时,大多数受体的供体型T细胞呈阴性,4个阳性受体中有3个由单一供体的祖细胞接种,这一发现支持了频率测定的可靠性。

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