Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2018 Aug 15;29(17):2055–2068. doi: 10.1091/mbc.E18-01-0007

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© 2018 Shi et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology.

This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License.

PMC Copyright notice

FIGURE 9: — Caly-ATEA but not Caly-WT increases the motility of GFP-Rab5-labeled organelles. (A) Left panels, colocalization of GFP-Rab5 (green) and mCh-Caly-WT (red). Arrows indicate overlapping puncta. Right panels, representative kymographs of Rab5-labeled organelles in axons transfected with mCherry (mCh), mCh-Caly-WT (Caly-WT), and mCh-Caly-ATEA (Caly-ATEA). (B) Average speeds of anterograde and retrograde motile events are higher in Caly-ATEA axons, whereas values detected in Caly-WT axons do not differ from control. (C) Retrogradely moving Rab5-labeled organelles are more common in Caly-ATEA axons relative to static and bidirectional organelles. (D) No difference in retrograde and anterograde motile events >10 μm were detected. Data shown in bar graphs (mean ± SEM) and box-and-whisker plots (mean, min, max ± 95% CI) reflect results obtained in three independent experiments, with at least five axons per group in each experiment; *p < 0.05, **p < 0.01, ***p < 0.001; A.S., axon segment; bar = 20 μm.