Bremer Sarah-Jolan, Glau Laura, Gehbauer Christina, Boxnick Annika, Biermann Daniel, Sachweh Jörg Siegmar, Tolosa Eva, Gieras Anna
Department of Immunology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Surgery for Congenital Heart Disease, University Heart & Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Cytometry A. 2021 Sep;99(9):875-879. doi: 10.1002/cyto.a.24326. Epub 2021 Mar 3.
This panel was designed for the identification and detailed characterization of the different developmental steps of human thymocytes. We optimized the panel for fresh tissue in order to provide an unbiased analysis of T cell development. Accurate selection of antibodies and precise gating allow us to phenotype 14 major stages of human thymocyte development and illustrate the trajectories of T cell development from early thymic progenitors (ETP) to mature T cells that are ready to populate the periphery. The panel identifies ETPs, T-lineage-committed cells (TC), CD34-positive immature single-positive CD4 cells (ISP4 CD34+), CD34-negative immature single-positive CD4 cells (ISP4 CD34-), CD45-low early double-positive cells (EDP CD45low), CD45-high early double-positive cells (EDP CD45high), late double-positive cells (LDP), single-positive CD4 cells (SP4), single-positive CD8 cells (SP8), ready-to-egress single-positive CD4 cells (rSP4), ready-to-egress single-positive CD8 cells (rSP8), T γδ cells (Tγδ), T regulatory cells (Treg), and ready-to-egress T regulatory cells (rTreg). To highlight important checkpoints during T cell development, we added antibodies relevant for specific developmental steps to the panel. These include CD1a to define TCs, CD28 as a marker for ß-selection and CD69 in combination with CD45RA to determine the maturation stage of thymocytes shortly before they become ready to egress the thymus and colonize the periphery. Moreover, Annexin V, as a marker for apoptosis, provides valuable extra information concerning the apoptotic death of thymocytes. Currently, we use this panel to identify aberrations in T cell development in health and disease.
该检测板旨在用于鉴定和详细表征人类胸腺细胞的不同发育阶段。我们针对新鲜组织对该检测板进行了优化,以便对T细胞发育进行无偏分析。准确选择抗体和精确设门使我们能够对人类胸腺细胞发育的14个主要阶段进行表型分析,并阐明T细胞从早期胸腺祖细胞(ETP)到准备进入外周的成熟T细胞的发育轨迹。该检测板可识别ETP、T系定向细胞(TC)、CD34阳性未成熟单阳性CD4细胞(ISP4 CD34+)、CD34阴性未成熟单阳性CD4细胞(ISP4 CD34-)、CD45低表达早期双阳性细胞(EDP CD45low)、CD45高表达早期双阳性细胞(EDP CD45high)、晚期双阳性细胞(LDP)、单阳性CD4细胞(SP4)、单阳性CD8细胞(SP8)、准备迁出的单阳性CD4细胞(rSP4)、准备迁出的单阳性CD8细胞(rSP8)、Tγδ细胞(Tγδ)、调节性T细胞(Treg)以及准备迁出的调节性T细胞(rTreg)。为突出T细胞发育过程中的重要检查点,我们在检测板中添加了与特定发育步骤相关的抗体。这些抗体包括用于定义TC的CD1a、作为β选择标志物的CD28以及与CD45RA联合用于确定胸腺细胞在准备迁出胸腺并定殖于外周前不久的成熟阶段的CD69。此外,膜联蛋白V作为细胞凋亡的标志物,提供了有关胸腺细胞凋亡死亡的有价值的额外信息。目前,我们使用该检测板来识别健康和疾病状态下T细胞发育的异常情况。