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. 2018 May 15;12:324. doi: 10.3389/fnins.2018.00324

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Copyright © 2018 Chen, Cheng, Chu, Zhang, Dong, Lou, Zhu and Liu.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Recording of cellular and subcellular behaviors using the ATPγS microinjection-based imaging system. (A) Dynamic changes of macropinosomes, from formation to fusion. Note that macropinosomes (red) were formed from the surface membrane ruffles and internalized after enclosure (arrowheads). The newly formed macropinosomes were indicated by dashed boxes and corresponding enlarged parts were presented at right corners. (B) TRD3S macropinosomes (red) transported within migrating hemocytes (green). The arrow indicates the location of a trafficking vesicle. Scale bars, 10 μm.