Single cell classification of macrophage subtypes by label-free cell signatures and machine learning

被引:5
|
作者
Dannhauser, David [1 ,2 ]
Rossi, Domenico [3 ]
De Gregorio, Vincenza [1 ,4 ]
Netti, Paolo Antonio [1 ,2 ,3 ]
Terrazzano, Giuseppe [5 ]
Causa, Filippo [1 ,2 ]
机构
[1] Univ Napoli Federico II, Interdisciplinary Res Ctr Biomat CRIB, Piazzale Tecchio 80, I-80125 Naples, Italy
[2] Univ Napoli Federico II, Dipartimento Ingn Chim, Mat Prod Ind, Piazzale Tecchio 80, I-80125 Naples, Italy
[3] Ctr Adv Biomat Healthcare CRIB, Ist Italiano Tecnol, Largo Barsanti Matteucci 53, I-80125 Naples, Italy
[4] Univ Napoli Federico II, Complesso Univ Monte S Angelo, Dipartimento Biol, Naples, Italy
[5] Univ Basilicata, Dipartimento Sci DiS, Via Ateneo Lucano 10, I-85100 Potenza, Italy
来源
ROYAL SOCIETY OPEN SCIENCE | 2022年 / 9卷 / 09期
关键词
single-cell; label-free; machine learning; optical signature; macrophages;
D O I
10.1098/rsos.220270
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Pro-inflammatory (M1) and anti-inflammatory (M2) macrophage phenotypes play a fundamental role in the immune response. The interplay and consequently the classification between these two functional subtypes is significant for many therapeutic applications. Albeit, a fast classification of macrophage phenotypes is challenging. For instance, image-based classification systems need cell staining and coloration, which is usually time- and cost-consuming, such as multiple cell surface markers, transcription factors and cytokine profiles are needed. A simple alternative would be to identify such cell types by using single-cell, label-free and high throughput light scattering pattern analyses combined with a straightforward machine learning-based classification. Here, we compared different machine learning algorithms to classify distinct macrophage phenotypes based on their optical signature obtained from an ad hoc developed wide-angle static light scattering apparatus. As the main result, we were able to identify unpolarized macrophages from M1- and M2-polarized phenotypes and distinguished them from naive monocytes with an average accuracy above 85%. Therefore, we suggest that optical single-cell signatures within a lab-on-a-chip approach along with machine learning could be used as a fast, affordable, non-invasive macrophage phenotyping tool to supersede resource-intensive cell labelling.
引用
收藏
页数:12
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