Label-free detection of cellular drug responses by high-throughput bright-field imaging and machine learning.
Hirofumi KobayashiCheng LeiYi WuAilin MaoYiyue JiangBaoshan GuoYasuyuki OzekiKeisuke GodaPublished in: Scientific reports (2017)
In the last decade, high-content screening based on multivariate single-cell imaging has been proven effective in drug discovery to evaluate drug-induced phenotypic variations. Unfortunately, this method inherently requires fluorescent labeling which has several drawbacks. Here we present a label-free method for evaluating cellular drug responses only by high-throughput bright-field imaging with the aid of machine learning algorithms. Specifically, we performed high-throughput bright-field imaging of numerous drug-treated and -untreated cells (N = ~240,000) by optofluidic time-stretch microscopy with high throughput up to 10,000 cells/s and applied machine learning to the cell images to identify their morphological variations which are too subtle for human eyes to detect. Consequently, we achieved a high accuracy of 92% in distinguishing drug-treated and -untreated cells without the need for labeling. Furthermore, we also demonstrated that dose-dependent, drug-induced morphological change from different experiments can be inferred from the classification accuracy of a single classification model. Our work lays the groundwork for label-free drug screening in pharmaceutical science and industry.
Keyphrases
- label free
- drug induced
- high throughput
- machine learning
- liver injury
- single cell
- induced apoptosis
- high resolution
- deep learning
- adverse drug
- cell cycle arrest
- artificial intelligence
- drug discovery
- big data
- oxidative stress
- endoplasmic reticulum stress
- endothelial cells
- optical coherence tomography
- bone marrow
- mesenchymal stem cells
- cell proliferation
- convolutional neural network
- photodynamic therapy
- stem cells
- sensitive detection
- pluripotent stem cells
- newly diagnosed
- cell therapy
- living cells
- emergency department
- induced pluripotent stem cells