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深入细胞洞察:人类干细胞和癌细胞中细胞骨架结构的超分辨率STORM成像

Advancing cellular insights: Super-resolution STORM imaging of cytoskeletal structures in human stem and cancer cells.

作者信息

Bharadwaj Anupam, Kumar Amalesh, Padalumavunkal Mathew Sam, Mitra Rumela, Bhattacharyya Jina, Jaganathan Bithiah Grace, Boruah Bosanta R

机构信息

Department of Physics, Indian Institute of Technology Guwahati, Guwahati, 781039, Assam, India.

Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Guwahati, 781039, Assam, India.

出版信息

Biochem Biophys Rep. 2024 Jul 25;39:101798. doi: 10.1016/j.bbrep.2024.101798. eCollection 2024 Sep.

Abstract

Fluorescence microscopy is an important tool for cell biology and cancer research. Present-day approach of implementing advanced optical microscopy methods combined with immunofluorescence labelling of specific proteins in cells is now able to deliver optical super-resolution up to ∼25 nm. Here we perform super-resolved imaging using standard immunostaining protocol combined with easy stochastic optical reconstruction microscopy (easySTORM) to observe structural differences of two cytoskeleton elements, actin and tubulin in three different cell types namely human bone marrow-derived mesenchymal stem cells (MSCs), human glioblastoma (U87MG) and breast cancer (MDAMB-231) cells. The average width of the actin bundle obtained from STORM images of stem cells is observed to be larger than the same for U87MG and MDAMB-231 cells. No significant difference is however noticed in the width of the tubulin within the same cells. We also study the functional effect on the 2D migration potential of MDAMB-231 cells silenced for NICD1 and β-catenin. Although similar migration speed is observed for cells with the above two conditions compared to their control cells, easySTORM images show that widths of the actin in MDAMB-231 cells in β-catenin silenced is significantly lower than the same in control cells. Such minute differences however are not observable in widefield images. The outcome of our easySTORM investigation should benefit the researchers carrying out detailed investigations of the cellular structure and potential therapeutic applications.

摘要

荧光显微镜是细胞生物学和癌症研究的重要工具。目前,将先进的光学显微镜方法与细胞中特定蛋白质的免疫荧光标记相结合的方法,现在能够实现高达约25纳米的光学超分辨率。在这里,我们使用标准免疫染色方案结合简易随机光学重建显微镜(easySTORM)进行超分辨成像,以观察三种不同细胞类型,即人骨髓间充质干细胞(MSC)、人胶质母细胞瘤(U87MG)和乳腺癌(MDAMB-231)细胞中两种细胞骨架成分肌动蛋白和微管蛋白的结构差异。从干细胞的STORM图像中获得的肌动蛋白束的平均宽度被观察到大于U87MG和MDAMB-231细胞的平均宽度。然而,在相同细胞内微管蛋白的宽度上没有观察到显著差异。我们还研究了对NICD1和β-连环蛋白沉默的MDAMB-231细胞的二维迁移潜力的功能影响。尽管与对照细胞相比,上述两种条件下的细胞观察到相似的迁移速度,但easySTORM图像显示,β-连环蛋白沉默的MDAMB-231细胞中肌动蛋白的宽度明显低于对照细胞。然而,这种微小差异在宽视野图像中是无法观察到的。我们easySTORM研究的结果应该会使那些对细胞结构进行详细研究和潜在治疗应用的研究人员受益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f865/11332080/7048f96724ab/gr1.jpg

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