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. 2017 May 4;11:135. doi: 10.3389/fncel.2017.00135

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Copyright © 2017 Gimenez-Molina, Villanueva, Nanclares, Lopez-Font, Viniegra, Francés, Gandia, Gil and Gutiérrez.

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) or licensor 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 distribution of α-fodrin in cultured cells and cells from adrenomedullary slices. Confocal images of α-fodrin (green fluorescence) and anti-SNAP-25 (red fluorescence) used to calculate the density of α-fodrin in the whole cell and at the plasma membrane (Membrane), as indicated in the previous Figure. Individual density profiles were used to obtain the averaged α-fodrin profiles from cultured cells (C, n = 11, 2 cell preparations) and in cells from adrenomedullary slices (D, n = 16, 2 adrenal medulla preparations). The average total α-fodrin patches appear to be much higher in the cells forming part of the adrenomedullary tissue (F), this being due to the abundant cytoplasmic α-fodrin. There are a similar number of membrane associated α-fodrin patches in cultured cells and cells from the adrenomedullary tissue (E,F). Bars in (A,B) represent 1 μm. ^∗∗∗P < 0.0001 using the two-way ANOVA test.