TY - JOUR
T1 - High-throughput label-free detection of DNA-to-RNA transcription inhibition using brightfield microscopy and deep neural networks
AU - Sauvat, Allan
AU - Cerrato, Giulia
AU - Humeau, Juliette
AU - Leduc, Marion
AU - Kepp, Oliver
AU - Kroemer, Guido
N1 - Publisher Copyright:
© 2021 The Authors
PY - 2021/6/1
Y1 - 2021/6/1
N2 - Drug discovery is in constant evolution and major advances have led to the development of in vitro high-throughput technologies, facilitating the rapid assessment of cellular phenotypes. One such phenotype is immunogenic cell death, which occurs partly as a consequence of inhibited RNA synthesis. Automated cell-imaging offers the possibility of combining high-throughput with high-content data acquisition through the simultaneous computation of a multitude of cellular features. Usually, such features are extracted from fluorescence images, hence requiring labeling of the cells using dyes with possible cytotoxic and phototoxic side effects. Recently, deep learning approaches have allowed the analysis of images obtained by brightfield microscopy, a technique that was for long underexploited, with the great advantage of avoiding any major interference with cellular physiology or stimulatory compounds. Here, we describe a label-free image-based high-throughput workflow that accurately detects the inhibition of DNA-to-RNA transcription. This is achieved by combining two successive deep convolutional neural networks, allowing (1) to automatically detect cellular nuclei (thus enabling monitoring of cell death) and (2) to classify the extracted nuclear images in a binary fashion. This analytical pipeline is R-based and can be easily applied to any microscopic platform.
AB - Drug discovery is in constant evolution and major advances have led to the development of in vitro high-throughput technologies, facilitating the rapid assessment of cellular phenotypes. One such phenotype is immunogenic cell death, which occurs partly as a consequence of inhibited RNA synthesis. Automated cell-imaging offers the possibility of combining high-throughput with high-content data acquisition through the simultaneous computation of a multitude of cellular features. Usually, such features are extracted from fluorescence images, hence requiring labeling of the cells using dyes with possible cytotoxic and phototoxic side effects. Recently, deep learning approaches have allowed the analysis of images obtained by brightfield microscopy, a technique that was for long underexploited, with the great advantage of avoiding any major interference with cellular physiology or stimulatory compounds. Here, we describe a label-free image-based high-throughput workflow that accurately detects the inhibition of DNA-to-RNA transcription. This is achieved by combining two successive deep convolutional neural networks, allowing (1) to automatically detect cellular nuclei (thus enabling monitoring of cell death) and (2) to classify the extracted nuclear images in a binary fashion. This analytical pipeline is R-based and can be easily applied to any microscopic platform.
KW - Cellular imaging
KW - Convolutional neural network
KW - Immunogenic cell death
KW - Semantic segmentation
KW - Systems biology
KW - Transmitted light microscopy
KW - UNET
UR - http://www.scopus.com/inward/record.url?scp=85104150814&partnerID=8YFLogxK
U2 - 10.1016/j.compbiomed.2021.104371
DO - 10.1016/j.compbiomed.2021.104371
M3 - Article
C2 - 33845268
AN - SCOPUS:85104150814
SN - 0010-4825
VL - 133
JO - Computers in Biology and Medicine
JF - Computers in Biology and Medicine
M1 - 104371
ER -