Three-dimensional human germinal centers of different sizes in patients diagnosed with lymphadenitis show comparative constant relative volumes of B cells, T cells, follicular dendritic cells, and macrophages

IF 2.3 4区 生物学 Q4 CELL BIOLOGY Acta histochemica Pub Date : 2023-10-01 DOI:10.1016/j.acthis.2023.152075
Constantin Maximilian Schemel , Patrick Wurzel , Sonja Scharf , Hendrik Schäfer , Sylvia Hartmann , Ina Koch , Martin-Leo Hansmann
{"title":"Three-dimensional human germinal centers of different sizes in patients diagnosed with lymphadenitis show comparative constant relative volumes of B cells, T cells, follicular dendritic cells, and macrophages","authors":"Constantin Maximilian Schemel ,&nbsp;Patrick Wurzel ,&nbsp;Sonja Scharf ,&nbsp;Hendrik Schäfer ,&nbsp;Sylvia Hartmann ,&nbsp;Ina Koch ,&nbsp;Martin-Leo Hansmann","doi":"10.1016/j.acthis.2023.152075","DOIUrl":null,"url":null,"abstract":"<div><p><span><span><span>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, </span>T cells<span>, 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 </span></span>lymphadenitis<span><span> 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<span> (nuclear staining). We detected average proportions of about 11% CD3, 9% CD20, 6% </span></span>CD23<span>, 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 </span></span></span>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.</p></div>","PeriodicalId":6961,"journal":{"name":"Acta histochemica","volume":"125 7","pages":"Article 152075"},"PeriodicalIF":2.3000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta histochemica","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0065128123000818","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

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.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
在被诊断为淋巴结炎的患者中,不同大小的三维人类生发中心显示B细胞、T细胞、滤泡树突状细胞和巨噬细胞的相对体积相对恒定。
生殖中心(GC)是人类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经得到了彻底的研究。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GC中。然而,这些细胞类型中每一种所占据的空间量还有待研究。在这项研究中,我们对淋巴结炎反应条件下的典型GC细胞进行了基于共焦激光的3D细胞体积定量,并研究了GC发育过程中体积比例的变化。在本研究中,我们使用了抗CD3(T细胞)、抗CD20和抗Pax5(B细胞)、反CD23(FDCs)、抗CD 68(巨噬细胞)和DAPI(核染色)。我们在GC内最大可能的感兴趣区域中检测到约11%的CD3、9%的CD20、6%的CD23和2%的CD68的平均比例。有趣的是,这些值相对独立于GC大小保持稳定。显著低的B细胞比例可归因于在3D中使用CD20抗体的技术限制。应用B细胞标记物Pax5,我们发现将B细胞核的体积外推到整个B细胞的体积后,约44%的体积被B细胞占据。我们得出结论,Pax5比抗CD20更适合用于GC中的3D B细胞定量。GC中大量未染色的体积提出了其他细胞类型是否填充这些开放空间的问题。我们的3D研究使GC细胞能够进行独特的形态学和体积评估,从而平衡其在GC中的总体积。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Acta histochemica
Acta histochemica 生物-细胞生物学
CiteScore
4.60
自引率
4.00%
发文量
107
审稿时长
23 days
期刊介绍: Acta histochemica, a journal of structural biochemistry of cells and tissues, publishes original research articles, short communications, reviews, letters to the editor, meeting reports and abstracts of meetings. The aim of the journal is to provide a forum for the cytochemical and histochemical research community in the life sciences, including cell biology, biotechnology, neurobiology, immunobiology, pathology, pharmacology, botany, zoology and environmental and toxicological research. The journal focuses on new developments in cytochemistry and histochemistry and their applications. Manuscripts reporting on studies of living cells and tissues are particularly welcome. Understanding the complexity of cells and tissues, i.e. their biocomplexity and biodiversity, is a major goal of the journal and reports on this topic are especially encouraged. Original research articles, short communications and reviews that report on new developments in cytochemistry and histochemistry are welcomed, especially when molecular biology is combined with the use of advanced microscopical techniques including image analysis and cytometry. Letters to the editor should comment or interpret previously published articles in the journal to trigger scientific discussions. Meeting reports are considered to be very important publications in the journal because they are excellent opportunities to present state-of-the-art overviews of fields in research where the developments are fast and hard to follow. Authors of meeting reports should consult the editors before writing a report. The editorial policy of the editors and the editorial board is rapid publication. Once a manuscript is received by one of the editors, an editorial decision about acceptance, revision or rejection will be taken within a month. It is the aim of the publishers to have a manuscript published within three months after the manuscript has been accepted
期刊最新文献
Corrigendum to "Protective effect of FXN overexpression on ferroptosis in L-Glu-induced SH-SY5Y cells" [Acta Histochem. 126 (2024) 152135]. Corrigendum to "MicroRNA-146b-5p suppresses cholangiocarcinoma cells by targeting TRAF6 and modulating p53 translocation" [Acta Histochem. (2021) 123 7 151793]. Exploring the oncogenic role of RGS19 in bladder cancer progression and prognosis miR-103–3p attenuates liver injury with severe acute pancreatitis by inhibiting pyroptosis through miR-103–3p/NLRP1 axis Ultrastructure and immunohistochemistry of apteric skin in ratites and its epidermal soft cornification
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1