SenPred: a single-cell RNA sequencing-based machine learning pipeline to classify deeply senescent dermal fibroblast cells for the detection of an in vivo senescent cell burden.

IF 10.4 1区 生物学 Q1 GENETICS & HEREDITY
Bethany K Hughes, Andrew Davis, Deborah Milligan, Ryan Wallis, Federica Mossa, Michael P Philpott, Linda J Wainwright, David A Gunn, Cleo L Bishop
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Abstract

Background: Senescence classification is an acknowledged challenge within the field, as markers are cell-type and context dependent. Currently, multiple morphological and immunofluorescence markers are required. However, emerging scRNA-seq datasets have enabled an increased understanding of senescent cell heterogeneity.

Methods: Here we present SenPred, a machine-learning pipeline which identifies fibroblast senescence based on single-cell transcriptomics from fibroblasts grown in 2D and 3D.

Results: Using scRNA-seq of both 2D and 3D deeply senescent fibroblasts, the model predicts intra-experimental fibroblast senescence to a high degree of accuracy (> 99% true positives). Applying SenPred to in vivo whole skin scRNA-seq datasets reveals that cells grown in 2D cannot accurately detect fibroblast senescence in vivo. Importantly, utilising scRNA-seq from 3D deeply senescent fibroblasts refines our ML model leading to improved detection of senescent cells in vivo. This is context specific, with the SenPred pipeline proving effective when detecting senescent human dermal fibroblasts in vivo, but not the senescence of lung fibroblasts or whole skin.

Conclusions: We position this as a proof-of-concept study based on currently available scRNA-seq datasets, with the intention to build a holistic model to detect multiple senescent triggers using future emerging datasets. The development of SenPred has allowed for the detection of an in vivo senescent fibroblast burden in human skin, which could have broader implications for the treatment of age-related morbidities. All code for the SenPred pipeline is available at the following URL: https://github.com/bethk-h/SenPred_HDF .

SenPred:一个基于单细胞RNA测序的机器学习管道,用于对深度衰老的真皮成纤维细胞进行分类,以检测体内衰老细胞负荷。
背景:衰老分类是该领域公认的挑战,因为标记物依赖于细胞类型和环境。目前,需要多种形态和免疫荧光标记。然而,新兴的scRNA-seq数据集增加了对衰老细胞异质性的理解。方法:在这里,我们提出了SenPred,一个机器学习管道,它基于2D和3D生长的成纤维细胞的单细胞转录组学来识别成纤维细胞衰老。结果:使用2D和3D深度衰老成纤维细胞的scRNA-seq,该模型预测实验内成纤维细胞衰老的准确性很高(> 99%真阳性)。将SenPred应用于体内全皮肤scRNA-seq数据集显示,在2D中生长的细胞不能准确检测体内成纤维细胞衰老。重要的是,利用3D深度衰老成纤维细胞的scRNA-seq改进了我们的ML模型,从而改善了体内衰老细胞的检测。这是特定环境的,SenPred管线在检测体内衰老的人类真皮成纤维细胞时被证明是有效的,但在检测肺成纤维细胞或整个皮肤的衰老时无效。结论:我们将此定位为基于当前可用的scRNA-seq数据集的概念验证研究,目的是建立一个整体模型,利用未来新出现的数据集检测多种衰老触发因素。SenPred的开发允许在人体皮肤中检测体内衰老成纤维细胞负荷,这可能对治疗年龄相关疾病具有更广泛的意义。SenPred管道的所有代码可在以下URL获得:https://github.com/bethk-h/SenPred_HDF。
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来源期刊
Genome Medicine
Genome Medicine GENETICS & HEREDITY-
CiteScore
20.80
自引率
0.80%
发文量
128
审稿时长
6-12 weeks
期刊介绍: Genome Medicine is an open access journal that publishes outstanding research applying genetics, genomics, and multi-omics to understand, diagnose, and treat disease. Bridging basic science and clinical research, it covers areas such as cancer genomics, immuno-oncology, immunogenomics, infectious disease, microbiome, neurogenomics, systems medicine, clinical genomics, gene therapies, precision medicine, and clinical trials. The journal publishes original research, methods, software, and reviews to serve authors and promote broad interest and importance in the field.
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