Image based Machine Learning for identification of macrophage subsets

被引:135
作者
Rostam, Hassan M. [1 ,4 ]
Reynolds, Paul M. [2 ]
Alexander, Morgan R. [3 ]
Gadegaard, Nikolaj [2 ]
Ghaemmaghami, Amir M. [1 ]
机构
[1] Univ Nottingham, Sch Life Sci, Div Immunol, Fac Med & Hlth Sci, Nottingham NG7 2RD, England
[2] Univ Glasgow, Sch Engn, Div Biomed Engn, Glasgow G12 8LT, Lanark, Scotland
[3] Univ Nottingham, Sch Pharm, Adv Mat & Healthcare Technol Div, Nottingham NG7 2RD, England
[4] Univ Garmian, Dept Biol, Kalar, Kurdistan, Iraq
基金
英国工程与自然科学研究理事会;
关键词
IN-VITRO; ACTIVATION; POLARIZATION; CELLS; CLASSIFICATION; INFLAMMATION; INDUCTION; PHENOTYPE; IMMUNITY; RELEASE;
D O I
10.1038/s41598-017-03780-z
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
Macrophages play a crucial rule in orchestrating immune responses against pathogens and foreign materials. Macrophages have remarkable plasticity in response to environmental cues and are able to acquire a spectrum of activation status, best exemplified by pro-inflammatory (M1) and antiinflammatory (M2) phenotypes at the two ends of the spectrum. Characterisation of M1 and M2 subsets is usually carried out by quantification of multiple cell surface markers, transcription factors and cytokine profiles. These approaches are time-consuming, require large numbers of cells and are resource intensive. In this study, we used machine learning algorithms to develop a simple and fast imaging-based approach that enables automated identification of different macrophage functional phenotypes using their cell size and morphology. Fluorescent microscopy was used to assess cell morphology of different cell types which were stained for nucleus and actin distribution using DAPI and phalloidin respectively. By only analysing their morphology we were able to identify M1 and M2 phenotypes effectively and could distinguish them from naive macrophages and monocytes with an average accuracy of 90%. Thus we suggest high-content and automated image analysis can be used for fast phenotyping of functionally diverse cell populations with reasonable accuracy and without the need for using multiple markers.
引用
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页数:11
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