Schemel Constantin Maximilian, Wurzel Patrick, Scharf Sonja, Schäfer Hendrik, Hartmann Sylvia, Koch Ina, Hansmann Martin-Leo
Institute of General Pharmacology and Toxicology, Goethe University Frankfurt/Main, Frankfurt/Main, Hessen, Germany.
Institute of General Pharmacology and Toxicology, Goethe University Frankfurt/Main, Frankfurt/Main, Hessen, Germany; Department of Molecular Bioinformatics, Institute of Computer Science, Goethe University Frankfurt/Main, Frankfurt/Main, Hessen, Germany; Frankfurt Institute for Advanced Studies (FIAS), Goethe University Frankfurt/Main, Frankfurt/Main, Hessen, Germany.
Acta Histochem. 2023 Oct;125(7):152075. doi: 10.1016/j.acthis.2023.152075. Epub 2023 Jul 15.
Germinal centers (GCs) are some of the most important structures in the human immune system. As such, their cell types and functions have been thoroughly investigated. B cells, T cells, follicular dendritic cells (FDCs), and macrophages have widely been found to typically be aggregated in GCs. However, the amount of space occupied by each of these cell types has yet to be investigated. In this study, we conducted confocal laser-based 3D cell-volume quantification of typical GC cells under reactive conditions in lymphadenitis and investigated how volume proportions change during GC development. For this investigation, we used anti-CD3 (T cells), anti-CD20 and anti-Pax5 (B cells), anti-CD23 (FDCs), anti-CD68 (macrophages), and DAPI (nuclear staining). We detected average proportions of about 11% CD3, 9% CD20, 6% CD23, and 2% CD68 in the largest possible regions of interest within GCs. Interestingly, these values remained steady relatively independent of GC size. The remarkably low B cell proportion can be attributed to technical constraints given the use of the CD20 antibody in 3D. Applying the B cell marker Pax5, we found that about 44% of the volume was occupied by B cells after extrapolating the volume of B cell nuclei to that of whole B cells. We concluded that Pax5 is more suitable than anti-CD20 for 3D B cell quantification in GCs. The substantial unstained volume in GCs raises the question of whether other cell types fill these open spaces. Our 3D investigation enabled a unique morphological and volumetric evaluation of GC cells that balance their overall volumes in GCs.
生发中心(GCs)是人体免疫系统中一些最重要的结构。因此,它们的细胞类型和功能已得到充分研究。人们广泛发现B细胞、T细胞、滤泡树突状细胞(FDCs)和巨噬细胞通常聚集在生发中心。然而,这些细胞类型各自所占的空间量尚未得到研究。在本研究中,我们对淋巴结炎反应条件下典型生发中心细胞进行了基于共聚焦激光的三维细胞体积定量分析,并研究了生发中心发育过程中体积比例是如何变化的。为了进行这项研究,我们使用了抗CD3(T细胞)、抗CD20和抗Pax5(B细胞)、抗CD23(FDCs)、抗CD68(巨噬细胞)以及DAPI(细胞核染色剂)。我们在生发中心内尽可能大的感兴趣区域检测到平均比例约为11%的CD3、9%的CD20、6%的CD23和2%的CD68。有趣的是,这些值相对稳定,与生发中心大小无关。鉴于在三维分析中使用了CD20抗体,B细胞比例极低可归因于技术限制。应用B细胞标志物Pax5,我们发现将B细胞核的体积外推至整个B细胞体积后,约44%的体积被B细胞占据。我们得出结论,在生发中心进行三维B细胞定量分析时,Pax5比抗CD20更合适。生发中心中大量未染色的体积引发了一个问题,即是否有其他细胞类型填充这些开放空间。我们的三维研究能够对生发中心细胞进行独特的形态学和体积评估,以平衡它们在生发中心的总体积。