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用不同创新的显微镜和光谱技术描述体外个体肾小球足细胞的形态。

Characterizing Intraindividual Podocyte Morphology In Vitro with Different Innovative Microscopic and Spectroscopic Techniques.

机构信息

Institute for Nanotechnology and Correlative Microscopy, INAM, 91301 Forchheim, Germany.

Department of Nephrology and Hypertension, Universitätsklinikum Erlangen, Friedrich-Alexander-University (FAU) Erlangen-Nürnberg, 91054 Erlangen, Germany.

出版信息

Cells. 2023 Apr 25;12(9):1245. doi: 10.3390/cells12091245.

Abstract

Podocytes are critical components of the glomerular filtration barrier, sitting on the outside of the glomerular basement membrane. Primary and secondary foot processes are characteristic for podocytes, but cell processes that develop in culture were not studied much in the past. Moreover, protocols for diverse visualization methods mostly can only be used for one technique, due to differences in fixation, drying and handling. However, we detected by single-cell RNA sequencing (scRNAseq) analysis that cells reveal high variability in genes involved in cell type-specific morphology, even within one cell culture dish, highlighting the need for a compatible protocol that allows measuring the same cell with different methods. Here, we developed a new serial and correlative approach by using a combination of a wide variety of microscopic and spectroscopic techniques in the same cell for a better understanding of podocyte morphology. In detail, the protocol allowed for the sequential analysis of identical cells with light microscopy (LM), Raman spectroscopy, scanning electron microscopy (SEM) and atomic force microscopy (AFM). Skipping the fixation and drying process, the protocol was also compatible with scanning ion-conductance microscopy (SICM), allowing the determination of podocyte surface topography of nanometer-range in living cells. With the help of nanoGPS Oxyo, tracking concordant regions of interest of untreated podocytes and podocytes stressed with TGF-β were analyzed with LM, SEM, Raman spectroscopy, AFM and SICM, and revealed significant morphological alterations, including retraction of podocyte process, changes in cell surface morphology and loss of cell-cell contacts, as well as variations in lipid and protein content in TGF-β treated cells. The combination of these consecutive techniques on the same cells provides a comprehensive understanding of podocyte morphology. Additionally, the results can also be used to train automated intelligence networks to predict various outcomes related to podocyte injury in the future.

摘要

足细胞是肾小球滤过屏障的关键组成部分,位于肾小球基底膜的外侧。初级和次级足突是足细胞的特征,但过去对培养中的细胞突起研究不多。此外,由于固定、干燥和处理方式的不同,大多数用于不同可视化方法的方案大多只能用于一种技术。然而,我们通过单细胞 RNA 测序(scRNAseq)分析发现,即使在同一个细胞培养皿中,参与细胞类型特异性形态的基因也存在高度变异性,这突出表明需要一种兼容的方案,允许用不同的方法测量同一个细胞。在这里,我们开发了一种新的串联和相关方法,在同一个细胞中使用多种微观和光谱技术的组合,以更好地了解足细胞的形态。具体来说,该方案允许用光镜(LM)、拉曼光谱、扫描电子显微镜(SEM)和原子力显微镜(AFM)对相同的细胞进行顺序分析。该方案跳过了固定和干燥过程,也与扫描离子电导显微镜(SICM)兼容,允许在活细胞中测定纳米级范围的足细胞表面形貌。借助 nanoGPS Oxyo,对未经处理的足细胞和经 TGF-β 处理的足细胞的共同感兴趣区域进行跟踪,用光镜、SEM、拉曼光谱、AFM 和 SICM 进行分析,结果显示出明显的形态改变,包括足细胞突起回缩、细胞表面形态变化和细胞间连接丧失,以及 TGF-β 处理细胞中脂质和蛋白质含量的变化。这些连续技术在同一细胞上的组合提供了对足细胞形态的全面了解。此外,这些结果还可以用于训练自动化智能网络,以预测未来与足细胞损伤相关的各种结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c785/10177567/19d0c11fe0c1/cells-12-01245-g001.jpg

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