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使用基于FIJI的半自动工具进行高效的细胞质细胞定量分析。

Efficient cytoplasmic cell quantification using a semi-automated FIJI-based tool.

作者信息

Unger Lucas, Larsen Ulrik, Sharmine Shayla, Hossain Md Kaykobad, Legøy Thomas Aga, Vaudel Marc, Ghila Luiza, Chera Simona

机构信息

Mohn Research Center for Diabetes Precision Medicine, Department of Clinical Science, Faculty of Medicine, University of Bergen, Glasblokkene 1, Haukelandsbakken 15, 5009, Bergen, Norway.

Department of Clinical Science, Faculty of Medicine, University of Bergen, Postboks 7804, 5020, Bergen, Norway.

出版信息

Sci Rep. 2025 Jul 28;15(1):27509. doi: 10.1038/s41598-025-12144-x.

DOI:10.1038/s41598-025-12144-x
PMID:40721622
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12304148/
Abstract

Quantification of subcellular structures such as nuclei and cytoplasmic proteins using staining methods based on fluorescent dyes or fluorescently tagged antibodies are widely used in scientific research. Accurate high-throughput quantitation of these assays can be time consuming and challenging. Here, we present our FIJI based Semi-Automated counting Macro termed SAM, and we validate its accuracy against manual counting and other automated counting methods. By introducing this automated quantification tool, we aim to contribute to the ongoing efforts to enhance the reliability, efficiency, and standardization of immunostaining analysis in the field of diabetes research and beyond.

摘要

使用基于荧光染料或荧光标记抗体的染色方法对细胞核和细胞质蛋白等亚细胞结构进行定量分析在科学研究中被广泛应用。对这些检测进行准确的高通量定量可能既耗时又具有挑战性。在此,我们展示了基于FIJI的半自动计数宏程序,称为SAM,并将其准确性与手动计数和其他自动计数方法进行了验证。通过引入这种自动定量工具,我们旨在为正在进行的努力做出贡献,以提高糖尿病研究及其他领域免疫染色分析的可靠性、效率和标准化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/12304148/e348ecc1de3a/41598_2025_12144_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/12304148/da86c9182a34/41598_2025_12144_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/12304148/aa47d2ef03b0/41598_2025_12144_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/12304148/be869ab65d75/41598_2025_12144_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/12304148/cce7cb659958/41598_2025_12144_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/12304148/ae1d2ee4df65/41598_2025_12144_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/12304148/c4ceac41c195/41598_2025_12144_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/12304148/e348ecc1de3a/41598_2025_12144_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/12304148/da86c9182a34/41598_2025_12144_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/12304148/66272de95297/41598_2025_12144_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/12304148/aa47d2ef03b0/41598_2025_12144_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/12304148/be869ab65d75/41598_2025_12144_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/12304148/cce7cb659958/41598_2025_12144_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/12304148/ae1d2ee4df65/41598_2025_12144_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/12304148/c4ceac41c195/41598_2025_12144_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d4/12304148/e348ecc1de3a/41598_2025_12144_Fig8_HTML.jpg

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本文引用的文献

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Moderate beta-cell ablation triggers synergic compensatory mechanisms even in the absence of overt metabolic disruption.中度β细胞消融会触发协同补偿机制,即使在没有明显代谢紊乱的情况下也是如此。
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Molecular profiling of NOD mouse islets reveals a novel regulator of insulitis onset.
对 NOD 小鼠胰岛的分子谱分析揭示了一种新的胰岛炎发病调节剂。
Sci Rep. 2024 Jun 25;14(1):14669. doi: 10.1038/s41598-024-65454-x.
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The age-dependent regulation of pancreatic islet landscape is fueled by a HNF1a-immune signaling loop.胰腺胰岛景观的年龄依赖性调节由一个HNF1a-免疫信号回路驱动。
Mech Ageing Dev. 2024 Aug;220:111951. doi: 10.1016/j.mad.2024.111951. Epub 2024 May 31.
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Illuminating the complete ß-cell mass of the human pancreas- signifying a new view on the islets of Langerhans.阐明人类胰腺中的完整β细胞群——标志着对胰岛的新认识。
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Targeted Gene Silencing by Using GapmeRs in Differentiating Human-Induced Pluripotent Stem Cells (hiPSC) Toward Pancreatic Progenitors.利用 GapmeRs 在分化的人诱导多能干细胞 (hiPSC) 中靶向基因沉默以获得胰腺祖细胞。
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