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. 2020 Aug 12;40(33):6270–6288. doi: 10.1523/JNEUROSCI.0925-20.2020

Figure 10.

Figure 10.

Morphologic consequences of silencing of MN1-Ib or MNIs. A–C, Representative confocal images of third instar larval M1 NMJs at segment A3 following immunolabeling with anti-HRP, anti-GFP, and anti-BRP in the following genotypes: UAS-TeTXLC control (A); MN1-Ib GAL4>UAS-TeTXLC (B); and MNIs GAL4>UAS-TeTXLC (C). MN1-Ib LexA>LexAop2-CD8-GFP was present in each genetic background to allow unambiguous identification of the Ib terminal. Diagrams of the experimental manipulation are shown on the left, with MN1-Ib (teal) and MNIs (orange) labeled. The merged image is shown on the right. The white dashed line highlights the MNIs terminal in the final three panels for each manipulation. Arrowheads in B depict GFP-positive filopodial-like projections from MN1-Ib following tetanus toxin expression. Scale bars: all panels, 10 µm. D, Quantification of filopodial-like projections in controls and following UAS-TeTXLC expression with MN1-Ib or MNIs GAL4. Each data point represents quantification from segment A3 M1 from a single third instar larvae. Statistical significance was determined using ANOVA. Data are shown as mean ± SEM. ***p < 0.001.