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CD24细胞清除可有效富集胸腺NKT细胞,同时保留其亚群组成。

CD24 Cell Depletion Permits Effective Enrichment of Thymic NKT Cells While Preserving Their Subset Composition.

作者信息

Park Joo-Young, Kwon Juntae, Kim Emily Y, Fink Juliet, Kim Hye Kyung, Park Jung-Hyun

机构信息

Department of Oral and Maxillofacial Surgery, Seoul National University Dental Hospital, Seoul 03080, Korea.

Experimental Immunology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Immune Netw. 2019 Mar 5;19(2):e14. doi: 10.4110/in.2019.19.e14. eCollection 2019 Apr.

Abstract

Invariant NKT (NKT) cells are a small subset of thymus-generated T cells that produce cytokines to control both innate and adaptive immunity. Because of their very low frequency in the thymus, in-depth characterization of NKT cells can be facilitated by their enrichment from total thymocytes. Magnetic-activated cell sorting (MACS) of glycolipid antigen-loaded CD1d-tetramer-binding cells is a commonly used method to enrich NKT cells. Surprisingly, we found that this procedure also dramatically altered the subset composition of enriched NKT cells. As such, NKT2 lineage cells that express large amounts of the transcription factor promyelocytic leukemia zinc finger were markedly over-represented, while NKT1 lineage cells expressing the transcription factor T-bet were significantly reduced. To overcome this limitation, here, we tested magnetic-activated depletion of CD24 immature thymocytes as an alternative method to enrich NKT cells. We found that the overall recovery in NKT cell numbers did not differ between these 2 methods. However, enrichment by CD24 cell depletion preserved the subset composition of NKT cells in the thymus, and thus permitted accurate and reproducible analysis of thymic NKT cells in further detail.

摘要

不变自然杀伤T(iNKT)细胞是胸腺产生的一小部分T细胞,可产生细胞因子以控制固有免疫和适应性免疫。由于其在胸腺中的频率极低,通过从总胸腺细胞中富集iNKT细胞,有助于对其进行深入表征。对负载糖脂抗原的CD1d四聚体结合细胞进行磁珠激活细胞分选(MACS)是富集iNKT细胞常用的方法。令人惊讶的是,我们发现该过程也显著改变了富集的iNKT细胞的亚群组成。具体而言,表达大量转录因子早幼粒细胞白血病锌指的iNKT2亚群细胞明显过度富集,而表达转录因子T-bet的iNKT1亚群细胞则显著减少。为克服这一局限性,在此我们测试了通过磁珠激活去除CD24未成熟胸腺细胞作为富集iNKT细胞的替代方法。我们发现这两种方法在iNKT细胞数量的总体回收率上没有差异。然而,通过去除CD24细胞进行富集可保留胸腺中iNKT细胞的亚群组成,从而能够更准确且可重复地进一步详细分析胸腺iNKT细胞。

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