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. 2019 Jan 9;11:484. doi: 10.3389/fnmol.2018.00484

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Copyright © 2019 Kuramochi and Doi.

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(s) 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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The localization patterns of the presynaptic protein RAB-3 in ASEL/R neurons and the postsynaptic AMPA-type glutamate receptors in AIB neurons. (A) The localization patterns of RAB-3 in the ASEL and the AMPA-type glutamate receptor GLR-1 in the AIB. (B) The localization patterns of RAB-3 in the ASER and the AMPA-type glutamate receptor GLR-1 in the AIB. (C) One-side images from left or right, and frontal images for the localization patterns of mCherry::RAB-3 on ASEL and GLR-1::GFP on the AIB. The left-half images show the co-localization pattern of mCherry::RAB-3 on the proximal ASEL and GLR-1::GFP in both the AIBL proximal neurite and AIBR distal neurite. The right side shows the co-localization pattern of mCherry::RAB-3 on the distal ASEL and GLR-1::GFP in both the AIBR proximal neurite and AIBL distal neurite. 0–1.0 shows the corresponding Z-axis frame position in (E). (D) One-side images from left or right, and frontal images for the localization patterns of mCherry::RAB-3 on ASER and GLR-1::GFP on AIB. The left-side images show the co-localization pattern of mCherry::RAB-3 on the distal ASEL and GLR-1::GFP in both the AIBL proximal neurite and AIBR distal neurite. The right side shows the co-localization pattern of mCherry::RAB-3 on the proximal ASER and GLR-1::GFP in both the AIBR proximal neurite and AIBL distal neurite. 0–1.0 shows the corresponding Z-axis frame position in (E). (E) Heatmap images of colocalization between mCherry (RAB-3) and GFP (GLR-1). Each colored line represents the overlap between green and red fluorescence in single slice image from Z-stack acquisition of corresponding transgenic worms. Numbers in left indicate individual animals. 0–1.0 is the relative flame position in full Z-stack image. (F) Quantification of overlap position in (E). The number of overlapped pixels in each z-axis frame are averaged. The error bars indicate the SEM; *p < 0.05; Wilcoxon rank sum test.