Deep learning for label-free nuclei detection from implicit phase information of mesenchymal stem cells

Monitoring of adherent cells in culture is routinely performed in biological and clinical laboratories, and it is crucial for large-scale manufacturing of cells needed in cell-based clinical trials and therapies. However, the lack of reliable and easily implementable label-free techniques makes this...

Full description

Bibliographic Details
Main Authors: Zhang, Zhengyun (Author), Leong, Kim Whye (Author), Vliet, Krystyn Van (Author), Barbastathis, George (Author), Ravasio, Andrea (Author)
Format: Article
Language:English
Published: The Optical Society, 2021-12-13T19:16:54Z.
Subjects:
Online Access:Get fulltext
LEADER 01961 am a22002053u 4500
001 138461
042 |a dc 
100 1 0 |a Zhang, Zhengyun  |e author 
700 1 0 |a Leong, Kim Whye  |e author 
700 1 0 |a Vliet, Krystyn Van  |e author 
700 1 0 |a Barbastathis, George  |e author 
700 1 0 |a Ravasio, Andrea  |e author 
245 0 0 |a Deep learning for label-free nuclei detection from implicit phase information of mesenchymal stem cells 
260 |b The Optical Society,   |c 2021-12-13T19:16:54Z. 
856 |z Get fulltext  |u https://hdl.handle.net/1721.1/138461 
520 |a Monitoring of adherent cells in culture is routinely performed in biological and clinical laboratories, and it is crucial for large-scale manufacturing of cells needed in cell-based clinical trials and therapies. However, the lack of reliable and easily implementable label-free techniques makes this task laborious and prone to human subjectivity. We present a deep-learning-based processing pipeline that locates and characterizes mesenchymal stem cell nuclei from a few bright-field images captured at various levels of defocus under collimated illumination. Our approach builds upon phase-from-defocus methods in the optics literature and is easily applicable without the need for special microscopy hardware, for example, phase contrast objectives, or explicit phase reconstruction methods that rely on potentially bias-inducing priors. Experiments show that this label-free method can produce accurate cell counts as well as nuclei shape statistics without the need for invasive staining or ultraviolet radiation. We also provide detailed information on how the deep-learning pipeline was designed, built and validated, making it straightforward to adapt our methodology to different types of cells. Finally, we discuss the limitations of our technique and potential future avenues for exploration. 
546 |a en 
655 7 |a Article 
773 |t 10.1364/BOE.420266 
773 |t Biomedical Optics Express