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. 2017 Dec 19;11:124. doi: 10.3389/fnana.2017.00124

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Copyright © 2017 Alonso, Lamus, Carnicero, Moro, de la Mano, Fernández, Desmond and Gato.

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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Effect of E-CSF on the number of migratory NSCs, monitored by co-expression of BrdU (green) and Doublecortin (DCX, red). Confocal photomicrographs show the RMS area of “in vitro” cultured adult mice brain slices (RMS in Figure 1B). Quantification of co-labeled BrdU and (DCX) NSCs in Control (A,B) and E-CSF treated brain slices (C,D) was plotted in graph bars (E) and expressed as means ± SD (n = 20); the significant threshold was set at p ≤ 0.001 (*) according to the two-tailed Student’s t-test. The results reveal a significant increase (127%) in the number of RMS migratory NSCs in CSF-E treated brain slices with respect to the controls. Scale bar: 100 μm (A,C) and 25 μm (B,D).