High‐content, label‐free analysis of proplatelet production from megakaryocytes

Background The mechanisms that regulate platelet biogenesis remain unclear; factors that trigger megakaryocytes (MKs) to initiate platelet production are poorly understood. Platelet formation begins with proplatelets, which are cellular extensions originating from the MK cell body. Objectives Propla...

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Veröffentlicht in:Journal of thrombosis and haemostasis 2020-10, Vol.18 (10), p.2701-2711
Hauptverfasser: French, Shauna L., Vijey, Prakrith, Karhohs, Kyle W., Wilkie, Adrian R., Horin, Lillian J., Ray, Anjana, Posorske, Benjamin, Carpenter, Anne E., Machlus, Kellie R., Italiano, Joseph E.
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Sprache:eng
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Zusammenfassung:Background The mechanisms that regulate platelet biogenesis remain unclear; factors that trigger megakaryocytes (MKs) to initiate platelet production are poorly understood. Platelet formation begins with proplatelets, which are cellular extensions originating from the MK cell body. Objectives Proplatelet formation is an asynchronous and dynamic process that poses unique challenges for researchers to accurately capture and analyze. We have designed an open‐source, high‐content, high‐throughput, label‐free analysis platform. Methods Phase‐contrast images of live, primary MKs are captured over a 24‐hour period. Pixel‐based machine‐learning classification done by ilastik generates probability maps of key cellular features (circular MKs and branching proplatelets), which are processed by a customized CellProfiler pipeline to identify and filter structures of interest based on morphology. A subsequent reinforcement classification, by CellProfiler Analyst, improves the detection of cellular structures. Results This workflow yields the percent of proplatelet production, area, count of proplatelets and MKs, and other statistics including skeletonization information for measuring proplatelet branching and length. We propose using a combination of these analyzed metrics, in particular the area measurements of MKs and proplatelets, when assessing in vitro proplatelet production. Accuracy was validated against manually counted images and an existing algorithm. We then used the new platform to test compounds known to cause thrombocytopenia, including bromodomain inhibitors, and uncovered previously unrecognized effects of drugs on proplatelet formation, thus demonstrating the utility of our analysis platform. Conclusion This advance in creating unbiased data analysis will increase the scale and scope of proplatelet production studies and potentially serve as a valuable resource for investigating molecular mechanisms of thrombocytopenia.
ISSN:1538-7933
1538-7836
1538-7836
DOI:10.1111/jth.15012