Skip to main content
. 2014 May 26;205(4):493–510. doi: 10.1083/jcb.201310045

Figure 5.

Figure 5.

Dendritic transport of ID4-chimeric mRNA after β-adrenergic activation. (A and B) After β-adrenergic activation with the agonist isoproterenol, ID4-chimeric α-tubulin mRNA was delivered to distal dendrites of sympathetic neurons. (C and D) In contrast, after α-adrenergic activation with the agonist phenylephrine, ID4-chimeric α-tubulin mRNA was not transported to dendrites to any substantial extent. (E and F) Application of the β-AR antagonist propranolol before application of agonist isoproterenol blocked the isoproterenol-induced dendritic delivery of ID4-chimeric α-tubulin mRNA. Concentrations of agonists, antagonists, and other drugs are given in Materials and methods. Number of cells analyzed: (A and B) 16 cells, 52 dendrites; (C and D) 16 cells, 57 dendrites; (E and F) 14 cells, 50 dendrites. Bar, 50 µm. (G) Quantitative analysis. One-way ANOVA, Dunnett’s post hoc analysis (comparison of RNA levels in the basal state [Fig. 2] with RNA levels after adrenergic activation/blockade): comparison with phenylephrine (A and B), P > 0.7 for interval points 50 µm; comparison with isoproterenol (C and D), P < 0.001 for all interval points; comparison with isoproterenol/propranolol (E and F), P > 0.8 for interval points 50 µm. Error bars indicate SEM.