Veronika E.M. Drexel , Thomas W. Göbel , Simon P. Früh
{"title":"新型鸡 γδ TCR 特异性标记物的特征。","authors":"Veronika E.M. Drexel , Thomas W. Göbel , Simon P. Früh","doi":"10.1016/j.dci.2024.105250","DOIUrl":null,"url":null,"abstract":"<div><p>Chickens are a species with a high number of γδ T cells in various tissues. Despite their abundance, γδ T cells are poorly characterized in chickens, partially due to a lack of specific reagents to characterize these cells. Up until now, the TCR1 clone has been the only γδ T cell-specific monoclonal antibody (mAb) in chickens and additional reagents for γδ T cell subsets are needed. In order to address this issue, new mAb were generated in our laboratory by immunizing mice with <em>in vitro</em> cultured γδ T cells. In an initial flow cytometric screen a new mAb, clone “8D2”, displayed an interesting staining pattern that mirrored γδ TCR up- and downregulation in the γδ T cell line D4 over time, prompting us to characterize this antibody further. We compared the expression of the unknown 8D2 epitope in combination with TCR1 staining across various primary cells. In splenocytes, peripheral blood lymphocytes and intestinal epithelial cells, 8D2 consistently labeled a subset of TCR1<sup>+</sup> cells. To determine, whether specific γδ T cell receptors were recognized by 8D2, we sorted γδ T cells according to their 8D2 and TCR1 expression and analyzed their TCR V(D)J gene usage by TCR profiling. Strikingly, sorted 8D2<sup>+</sup> cells preferentially expressed Vγ3 genes, whereas the TCR Vγ genes used by TCR1<sup>+</sup> 8D2<sup>-</sup> cells were more variable. γδ TCR in 8D2<sup>+</sup> cells were most frequently comprised of gamma chain VJ genes TRGV3-8 and TRGJ3, and delta chain VDJ genes TRDV1-2, TRDD2, TRDJ1. To confirm binding of 8D2 to specific γδ TCR, the preferentially utilized combination of TRG and TRD was expressed in HEK293 cells in combination with CD3, demonstrating surface binding of the 8D2 mAb to this Vγ3 γδ TCR-expressing cell line. Conversely, HEK293 cells expressing either Vγ1 or Vγ2 TCR did not react with 8D2. In conclusion, 8D2 is a novel tool for identifying specific Vγ3 bearing γδ T cells.</p></div>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-08-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0145305X24001228/pdfft?md5=a69b229c9846deca8c39ad870a388c55&pid=1-s2.0-S0145305X24001228-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Characterization of a novel chicken γδ TCR-specific marker\",\"authors\":\"Veronika E.M. Drexel , Thomas W. Göbel , Simon P. Früh\",\"doi\":\"10.1016/j.dci.2024.105250\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Chickens are a species with a high number of γδ T cells in various tissues. Despite their abundance, γδ T cells are poorly characterized in chickens, partially due to a lack of specific reagents to characterize these cells. Up until now, the TCR1 clone has been the only γδ T cell-specific monoclonal antibody (mAb) in chickens and additional reagents for γδ T cell subsets are needed. In order to address this issue, new mAb were generated in our laboratory by immunizing mice with <em>in vitro</em> cultured γδ T cells. In an initial flow cytometric screen a new mAb, clone “8D2”, displayed an interesting staining pattern that mirrored γδ TCR up- and downregulation in the γδ T cell line D4 over time, prompting us to characterize this antibody further. We compared the expression of the unknown 8D2 epitope in combination with TCR1 staining across various primary cells. In splenocytes, peripheral blood lymphocytes and intestinal epithelial cells, 8D2 consistently labeled a subset of TCR1<sup>+</sup> cells. To determine, whether specific γδ T cell receptors were recognized by 8D2, we sorted γδ T cells according to their 8D2 and TCR1 expression and analyzed their TCR V(D)J gene usage by TCR profiling. Strikingly, sorted 8D2<sup>+</sup> cells preferentially expressed Vγ3 genes, whereas the TCR Vγ genes used by TCR1<sup>+</sup> 8D2<sup>-</sup> cells were more variable. γδ TCR in 8D2<sup>+</sup> cells were most frequently comprised of gamma chain VJ genes TRGV3-8 and TRGJ3, and delta chain VDJ genes TRDV1-2, TRDD2, TRDJ1. To confirm binding of 8D2 to specific γδ TCR, the preferentially utilized combination of TRG and TRD was expressed in HEK293 cells in combination with CD3, demonstrating surface binding of the 8D2 mAb to this Vγ3 γδ TCR-expressing cell line. Conversely, HEK293 cells expressing either Vγ1 or Vγ2 TCR did not react with 8D2. In conclusion, 8D2 is a novel tool for identifying specific Vγ3 bearing γδ T cells.</p></div>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-08-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S0145305X24001228/pdfft?md5=a69b229c9846deca8c39ad870a388c55&pid=1-s2.0-S0145305X24001228-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0145305X24001228\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0145305X24001228","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0
摘要
鸡是各种组织中存在大量γδ T 细胞的物种。尽管γδ T 细胞数量很多,但鸡体内γδ T 细胞的特征却很不明显,部分原因是缺乏表征这些细胞的特异性试剂。到目前为止,TCR1 克隆一直是鸡体内唯一的γδ T 细胞特异性单克隆抗体(mAb),还需要更多的γδ T 细胞亚群试剂。为了解决这个问题,我们实验室用体外培养的 γδ T 细胞免疫小鼠,产生了新的 mAb。在最初的流式细胞筛选中,一种新的 mAb(克隆 "8D2")显示了一种有趣的染色模式,它反映了随着时间推移γδ T 细胞系 D4 中γδ TCR 的上调和下调,这促使我们进一步研究这种抗体的特性。我们比较了未知 8D2 表位与 TCR1 染色在各种原代细胞中的表达情况。在脾细胞、外周血淋巴细胞和肠上皮细胞中,8D2 始终标记 TCR1+ 细胞亚群。为了确定 8D2 是否能识别特定的 γδ T 细胞受体,我们根据 8D2 和 TCR1 的表达对 γδ T 细胞进行了分选,并通过 TCR 图谱分析了它们的 TCR V(D)J 基因使用情况。引人注目的是,分选的8D2+细胞优先表达Vγ3基因,而TCR1+ 8D2-细胞使用的TCR Vγ基因则变化较大。8D2+ 细胞中的γδ TCR 最常由γ链 VJ 基因 TRGV3-8 和 TRGJ3 以及δ链 VDJ 基因 TRDV1-2、TRDD2 和 TRDJ1 组成。为了证实 8D2 与特异性 γδ TCR 的结合,在 HEK293 细胞中将 TRG 和 TRD 的优先利用组合与 CD3 结合表达,证明 8D2 mAb 与这种表达 Vγ3 γδ TCR 的细胞系表面结合。相反,表达 Vγ1 或 Vγ2 TCR 的 HEK293 细胞与 8D2 没有反应。总之,8D2 是识别特异性 Vγ3 γδ T 细胞的一种新工具。
Characterization of a novel chicken γδ TCR-specific marker
Chickens are a species with a high number of γδ T cells in various tissues. Despite their abundance, γδ T cells are poorly characterized in chickens, partially due to a lack of specific reagents to characterize these cells. Up until now, the TCR1 clone has been the only γδ T cell-specific monoclonal antibody (mAb) in chickens and additional reagents for γδ T cell subsets are needed. In order to address this issue, new mAb were generated in our laboratory by immunizing mice with in vitro cultured γδ T cells. In an initial flow cytometric screen a new mAb, clone “8D2”, displayed an interesting staining pattern that mirrored γδ TCR up- and downregulation in the γδ T cell line D4 over time, prompting us to characterize this antibody further. We compared the expression of the unknown 8D2 epitope in combination with TCR1 staining across various primary cells. In splenocytes, peripheral blood lymphocytes and intestinal epithelial cells, 8D2 consistently labeled a subset of TCR1+ cells. To determine, whether specific γδ T cell receptors were recognized by 8D2, we sorted γδ T cells according to their 8D2 and TCR1 expression and analyzed their TCR V(D)J gene usage by TCR profiling. Strikingly, sorted 8D2+ cells preferentially expressed Vγ3 genes, whereas the TCR Vγ genes used by TCR1+ 8D2- cells were more variable. γδ TCR in 8D2+ cells were most frequently comprised of gamma chain VJ genes TRGV3-8 and TRGJ3, and delta chain VDJ genes TRDV1-2, TRDD2, TRDJ1. To confirm binding of 8D2 to specific γδ TCR, the preferentially utilized combination of TRG and TRD was expressed in HEK293 cells in combination with CD3, demonstrating surface binding of the 8D2 mAb to this Vγ3 γδ TCR-expressing cell line. Conversely, HEK293 cells expressing either Vγ1 or Vγ2 TCR did not react with 8D2. In conclusion, 8D2 is a novel tool for identifying specific Vγ3 bearing γδ T cells.