基于光学成熟度特征的iPSC-CMs无创成熟度评估

IF 4.1 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Computational and structural biotechnology journal Pub Date : 2025-08-22 eCollection Date: 2025-01-01 DOI:10.1016/j.csbj.2025.08.024
Fabian Scheurer, Alexander Hammer, Mario Schubert, Robert-Patrick Steiner, Oliver Gamm, Kaomei Guan, Frank Sonntag, Hagen Malberg, Martin Schmidt
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引用次数: 0

摘要

人诱导多能干细胞来源的心肌细胞(iPSC-CMs)是鉴定新的治疗靶点和心脏保护药物的重要资源。然而,iPSC-CMs的一个关键限制是它们不成熟的胎儿样表型。在脂质补充成熟培养基(MM)中培养iPSC-CMs可提高iPSC-CMs的结构、代谢和电生理特性。然而,它们面临着巨大的局限性,因为它们劳动密集,耗时,并且与细胞损伤或样品丢失一致。为了解决这个问题,我们开发了一种非侵入性方法,通过基于视频运动分析的可解释的基于人工智能(AI)的节奏特征分析,对iPSC-CM成熟度进行自动分类。在一项前瞻性研究中,我们评估了230个早期状态的未成熟iPSC-CMs在分化后21天(d21)和更成熟的iPSC-CMs在MM中培养(d42, MM)的视频记录。对每条录音,使用Maia运动分析软件提取10个特征,并输入支持向量机(SVM)。通过5倍交叉验证,对80% %的数据进行网格搜索,优化支持向量机的超参数。优化后的模型在hold-out测试集上的准确率为99.5 ± 1.1 %。Shapley加性解释(SHAP)确定位移、松弛上升时间和跳动持续时间是评估iPSC-CM成熟度最相关的特征。我们的研究结果表明,使用非侵入性光学运动分析结合基于人工智能的方法作为评估iPSC-CMs成熟度的工具,可以在进行功能读数或药物测试之前应用。这可能会潜在地减少可变性并提高实验研究的可重复性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Non-invasive maturity assessment of iPSC-CMs based on optical maturity characteristics using interpretable AI.

Human induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) are an important resource for identifying novel therapeutic targets and cardioprotective drugs. However, a key limitation of iPSC-CMs is their immature, fetal-like phenotype. Cultivation of iPSC-CMs in lipid-supplemented maturation media (MM) enhances the structural, metabolic and electrophysiological properties of iPSC-CMs. Nevertheless, they face substantial limitations as there are labor-intensive, time consuming and go in line with cell damage or loss of the sample. To address this issue, we have developed a non-invasive approach for automated classification of iPSC-CM maturity through interpretable artificial intelligence (AI)-based analysis of beat characteristics derived from video-based motion analysis. In a prospective study, we evaluated 230 video recordings of early-state, immature iPSC-CMs on day 21 after differentiation (d21) and more mature iPSC-CMs cultured in MM (d42, MM). For each recording, 10 features were extracted using Maia motion analysis software and entered into a support vector machine (SVM). The hyperparameters of the SVM were optimized in a grid search on 80 % of the data using 5-fold cross-validation. The optimized model achieved an accuracy of 99.5 ± 1.1 % on a hold-out test set. Shapley Additive Explanations (SHAP) identified displacement, relaxation-rise time and beating duration as the most relevant features for assessing iPSC-CM maturity. Our results suggest the use of non-invasive, optical motion analysis combined with AI-based methods as a tool to assess iPSC-CMs maturity and could be applied before performing functional readouts or drug testing. This may potentially reduce the variability and improve the reproducibility of experimental studies.

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来源期刊
Computational and structural biotechnology journal
Computational and structural biotechnology journal Biochemistry, Genetics and Molecular Biology-Biophysics
CiteScore
9.30
自引率
3.30%
发文量
540
审稿时长
6 weeks
期刊介绍: Computational and Structural Biotechnology Journal (CSBJ) is an online gold open access journal publishing research articles and reviews after full peer review. All articles are published, without barriers to access, immediately upon acceptance. The journal places a strong emphasis on functional and mechanistic understanding of how molecular components in a biological process work together through the application of computational methods. Structural data may provide such insights, but they are not a pre-requisite for publication in the journal. Specific areas of interest include, but are not limited to: Structure and function of proteins, nucleic acids and other macromolecules Structure and function of multi-component complexes Protein folding, processing and degradation Enzymology Computational and structural studies of plant systems Microbial Informatics Genomics Proteomics Metabolomics Algorithms and Hypothesis in Bioinformatics Mathematical and Theoretical Biology Computational Chemistry and Drug Discovery Microscopy and Molecular Imaging Nanotechnology Systems and Synthetic Biology
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