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表达外周淋巴结归巢受体的胸腺细胞的表型分析。

Phenotypic analysis of thymocytes that express homing receptors for peripheral lymph nodes.

作者信息

Reichert R A, Weissman I L, Butcher E C

出版信息

J Immunol. 1986 May 15;136(10):3521-8.

PMID:3084632
Abstract

Thymocytes that express high levels of homing receptors for peripheral lymph nodes can be detected with the monoclonal antibody MEL-14. We have shown that in adult mice these rare MEL-14hi thymocytes a) are cortical in location and typically constitute 1 to 3% of the total thymocyte population, b) may be a major source of thymus emigrants, and c) contain a high frequency of precursors of alloreactive cytotoxic T lymphocytes. In this study we have analyzed the phenotype of the MEL-14hi thymocyte subset. Most normal adult MEL-14hi thymocytes are midsize and express the mature phenotype typical of thymus emigrants, medullary thymocytes, and peripheral T cells: they are predominantly PNAlo, H-2K+, Thy-1+, Ly-1hi, and either Lyt-2-/L3T4+ or Lyt-2+/L3T4-. These findings argue strongly for the presence of rare MEL-14hi immunocompetent cortical thymocytes that, aside from their homing receptor expression, are phenotypically indistinguishable from medullary thymocytes. However, a minority (20 to 30%) of MEL-14hi thymocytes are large and phenotypically nonmature: they express intermediate to high levels of PNA binding sites, and are H-2K- to H-2Klo, Thy-1hi, Ly-1+, and either Lyt-2+/L3T4+ or Lyt-2-/L3T4-. Through a technique that selectively labels outer cortical cells, phenotypically nonmature MEL-14hi thymocytes have been shown to be concentrated in the subcapsular blast region of the outer cortex. Although we have no direct evidence of a precursor-product relationship, we consider it likely that the phenotypically nonmature outer cortical MEL-14hi lymphoblasts give rise to phenotypically mature MEL-14hi cells located deeper in the cortex. These results are consistent with our previous proposal that MEL-14hi thymocytes are a major source of thymus emigrants, and indicate that expression of high levels of MEL-14-defined homing receptors may be closely linked to the intrathymic selection process.

摘要

可使用单克隆抗体MEL-14检测到表达高水平外周淋巴结归巢受体的胸腺细胞。我们已经表明,在成年小鼠中,这些罕见的MEL-14高表达胸腺细胞:a) 位于皮质,通常占胸腺细胞总数的1%至3%;b) 可能是胸腺迁出细胞的主要来源;c) 含有高频率的同种异体反应性细胞毒性T淋巴细胞前体。在本研究中,我们分析了MEL-14高表达胸腺细胞亚群的表型。大多数正常成年MEL-14高表达胸腺细胞中等大小,并表达胸腺迁出细胞、髓质胸腺细胞和外周T细胞典型的成熟表型:它们主要是PNA低表达、H-2K高表达、Thy-1高表达、Ly-1高表达,且要么是Lyt-2阴性/L3T4阳性,要么是Lyt-2阳性/L3T4阴性。这些发现有力地证明了存在罕见的MEL-14高表达免疫 competent皮质胸腺细胞,除了它们的归巢受体表达外,其表型与髓质胸腺细胞无法区分。然而,少数(20%至30%)的MEL-14高表达胸腺细胞较大且表型不成熟:它们表达中等至高水平的PNA结合位点,且H-2K从阴性到低表达,Thy-1高表达,Ly-1高表达,且要么是Lyt-2阳性/L3T4阳性,要么是Lyt-2阴性/L3T4阳性。通过一种选择性标记外皮质细胞的技术,已表明表型不成熟的MEL-14高表达胸腺细胞集中在外皮质的被膜下胚细胞区域。虽然我们没有直接证据证明前体-产物关系,但我们认为表型不成熟的外皮质MEL-14高表达淋巴母细胞很可能产生位于皮质更深部位的表型成熟的MEL-14高表达细胞。这些结果与我们之前提出的MEL-14高表达胸腺细胞是胸腺迁出细胞的主要来源这一观点一致,并表明高水平的MEL-14定义的归巢受体表达可能与胸腺内选择过程密切相关。

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