Morphological profiling by high-throughput single-cell biophysical fractometry

Complex and irregular cell architecture is known to statistically exhibit fractal geometry, i.e., a pattern resembles a smaller part of itself. Although fractal variations in cells are proven to be closely associated with the disease-related phenotypes that are otherwise obscured in the standard cel...

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Veröffentlicht in:Communications biology 2023-04, Vol.6 (1), p.449-449, Article 449
Hauptverfasser: Zhang, Ziqi, Lee, Kelvin C. M., Siu, Dickson M. D., Lo, Michelle C. K., Lai, Queenie T. K., Lam, Edmund Y., Tsia, Kevin K.
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Sprache:eng
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Zusammenfassung:Complex and irregular cell architecture is known to statistically exhibit fractal geometry, i.e., a pattern resembles a smaller part of itself. Although fractal variations in cells are proven to be closely associated with the disease-related phenotypes that are otherwise obscured in the standard cell-based assays, fractal analysis with single-cell precision remains largely unexplored. To close this gap, here we develop an image-based approach that quantifies a multitude of single-cell biophysical fractal-related properties at subcellular resolution. Taking together with its high-throughput single-cell imaging performance (~10,000 cells/sec), this technique, termed single-cell biophysical fractometry, offers sufficient statistical power for delineating the cellular heterogeneity, in the context of lung-cancer cell subtype classification, drug response assays and cell-cycle progression tracking. Further correlative fractal analysis shows that single-cell biophysical fractometry can enrich the standard morphological profiling depth and spearhead systematic fractal analysis of how cell morphology encodes cellular health and pathological conditions. A high-throughput image-based approach quantifies single-cell biophysical fractal-related properties at subcellular resolution with statistical power for cell classification, drug response assays, and cell-cycle progression tracking.
ISSN:2399-3642
2399-3642
DOI:10.1038/s42003-023-04839-6