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ROCKETS - 一种用于药物发现的新型通用化的光片显微镜工具盒。

ROCKETS - a novel one-for-all toolbox for light sheet microscopy in drug discovery.

机构信息

Interdisciplinary Center for Clinical Research Laboratory (IZKF) Würzburg, Department of Internal Medicine II, Center for Experimental Molecular Medicine, Würzburg University Hospital, Würzburg, Germany.

Pharmaceutical Research and Early Development, Roche Diagnostics GmbH, Penzberg, Germany.

出版信息

Front Immunol. 2023 Feb 7;14:1034032. doi: 10.3389/fimmu.2023.1034032. eCollection 2023.

Abstract

Advancing novel immunotherapy strategies requires refined tools in preclinical research to thoroughly assess drug targets, biodistribution, safety, and efficacy. Light sheet fluorescence microscopy (LSFM) offers unprecedented fast volumetric imaging of large tissue samples in high resolution. Yet, to date laborious and unstandardized tissue processing procedures have limited throughput and broader applications in immunological research. Therefore, we developed a simple and harmonized protocol for processing, clearing and imaging of all mouse organs and even entire mouse bodies. Applying this Rapid Optical Clearing Kit for Enhanced Tissue Scanning (ROCKETS) in combination with LSFM allowed us to comprehensively study the biodistribution of an antibody targeting Epithelial Cell Adhesion Molecule (EpCAM) in 3D. Quantitative high-resolution scans of whole organs did not only reveal known EpCAM expression patterns but, importantly, uncovered several new EpCAM-binding sites. We identified gustatory papillae of the tongue, choroid plexi in the brain and duodenal papillae as previously unanticipated locations of high EpCAM expression. Subsequently, we confirmed high EpCAM expression also in human tongue and duodenal specimens. Choroid plexi and duodenal papillae may be considered as particularly sensitive sites due to their importance for liquor production or as critical junctions draining bile and digestive pancreatic enzymes into the small bowel, respectively. These newly gained insights appear highly relevant for clinical translation of EpCAM-addressing immunotherapies. Thus, ROCKETS in combination with LSFM may help to set new standards for preclinical evaluation of immunotherapeutic strategies. In conclusion, we propose ROCKETS as an ideal platform for a broader application of LSFM in immunological research optimally suited for quantitative co-localization studies of immunotherapeutic drugs and defined cell populations in the microanatomical context of organs or even whole mice.

摘要

推进新型免疫治疗策略需要在临床前研究中使用精细的工具,以彻底评估药物靶点、生物分布、安全性和疗效。光片荧光显微镜(LSFM)提供了前所未有的快速大容量成像高分辨率的大组织样本。然而,迄今为止,繁琐和非标准化的组织处理程序限制了其在免疫研究中的通量和更广泛的应用。因此,我们开发了一种简单而协调的方案,用于处理、清除和成像所有小鼠器官,甚至整个小鼠体。应用这种用于增强组织扫描的快速光学清除试剂盒(ROCKETS)与 LSFM 相结合,使我们能够全面研究针对上皮细胞黏附分子(EpCAM)的抗体的生物分布。对整个器官的定量高分辨率扫描不仅揭示了已知的 EpCAM 表达模式,而且重要的是,还揭示了几个新的 EpCAM 结合位点。我们确定了舌的味觉乳头、脑的脉络丛和十二指肠乳头是 EpCAM 高表达的先前未预料到的部位。随后,我们在人舌和十二指肠标本中证实了高 EpCAM 表达。脉络丛和十二指肠乳头可能被认为是特别敏感的部位,因为它们对于产生脑脊液或作为胆汁和消化胰腺酶分别排入小肠的关键交界处具有重要意义。这些新获得的见解似乎对 EpCAM 靶向免疫治疗的临床转化具有高度相关性。因此,ROCKETS 与 LSFM 结合可能有助于为免疫治疗策略的临床前评估设定新标准。总之,我们建议 ROCKETS 作为 LSFM 在免疫研究中更广泛应用的理想平台,非常适合定量共定位研究免疫治疗药物和定义的细胞群体在器官的微观解剖学背景下,甚至整个小鼠。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30f3/9945347/fbd5b8bcf470/fimmu-14-1034032-g001.jpg

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