3D examination reveals increased destruction of alpha-actin-positive structures in advanced follicular lymphoma stages

IF 2.3 4区 生物学 Q4 CELL BIOLOGY
Katharina Geib , Sonja Scharf , Hendrik Schäfer , Sylvia Hartmann , Martin-Leo Hansmann , Patrick Wurzel
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引用次数: 0

Abstract

Follicular lymphoma (FL) represents the most prevalent subtype of non-Hodgkin’s-lymphoma in Western Europe and the United States. While the examination of two-dimensional histological slides remains the gold standard method for diagnosing FL stages, three-dimensional analysis provides additional insights, particularly regarding cellular morphology, spatial relationships and network connectivity. This investigation assessed the tumor-related morphological destruction of fibroreticular cell (FRC) networks bordering germinal centres in FL. A confocal laser scanning technology and a digital three-dimensional analysis system were used. Quantitive measurements included the length of fibroblastic reticular walls surrounding the germinal centres as well as the size of the gaps and holes within these structures. Three-dimensional analysis revealed progressive structural degradation and a reduction in mechanical barrier integrity, with differences observed between low- and high-grade FL. High-grade FL exhibited greater network destruction. Fibroblastic reticular cell networks’ wall length demonstrated a consistent decline across all grades. The lengths of these walls and wall-like structures in FL grades 1 or 2 were similar to reactive germinal centres seen in lymphadenitis, as well as the gap size. The gaps are thought to be responsible for B- and T-cell exchange. This work demonstrated the massive destruction of neoplastic germinal centres in grades 3a and 3b FL. In grade 3b, this was accompanied by a likely dysfunctional mechanical border of the germinal centre and the near-complete loss of structural integrity. Under physiological conditions, gaps and holes regulate lymphoid traffic. Under reactive conditions, only a few specific T-cells can access the germinal centre. Under neoplastic conditions, the diameter of these gaps increases as grades increase, culminating in complete structural disruption in grade 3b. The mechanical destruction was found to begin at one pole of the germinal centre, as evidenced by localized decay and fragmentation of FRC walls on one side. Fibroblastic reticular cell networks are critical for maintaining chemokine gradients to ensure compartmentalisation of lymphoid structures. Their ongoing degradation in FL of the networks leads to a morphological loss of function. This is due to the blurring of various lymph node zones.
3D检查显示在晚期滤泡性淋巴瘤阶段α -肌动蛋白阳性结构的破坏增加。
滤泡性淋巴瘤(FL)是西欧和美国最常见的非霍奇金淋巴瘤亚型。虽然二维组织学切片检查仍然是诊断FL分期的金标准方法,但三维分析提供了额外的见解,特别是关于细胞形态,空间关系和网络连接。本研究评估了FL中与生发中心接壤的纤维网状细胞(FRC)网络的肿瘤相关形态学破坏。采用共聚焦激光扫描技术和数字三维分析系统。定量测量包括围绕生发中心的成纤维网状壁的长度以及这些结构内的间隙和孔的大小。三维分析显示,低级别和高级别FL之间存在结构退化和机械屏障完整性降低的差异。高级别FL表现出更大的网络破坏。纤维母细胞网状细胞网络的壁长在所有等级中都表现出一致的下降。FL 1级或2级的壁和壁样结构的长度和间隙大小与淋巴结炎的反应性生发中心相似。这些间隙被认为是B细胞和t细胞交换的原因。本研究表明3a级和3b级FL中肿瘤生发中心的大量破坏。在3b级FL中,这可能伴随着生发中心的机械边界功能障碍和结构完整性几乎完全丧失。在生理条件下,间隙和孔洞调节淋巴细胞的运输。在反应条件下,只有少数特定的t细胞可以进入生发中心。在肿瘤条件下,这些间隙的直径随着级别的增加而增加,最终在3b级时发生完全的结构破坏。发现机械破坏始于生发中心的一端,一侧FRC壁的局部腐烂和碎裂证明了这一点。成纤维网状细胞网络对于维持趋化因子梯度以确保淋巴样结构的区隔化至关重要。它们在网络FL中的持续降解导致功能的形态学丧失。这是由于不同淋巴结区域的模糊。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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
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