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. 2018 Feb 27;8:3692. doi: 10.1038/s41598-018-22049-7

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Specific structural organization of OSNs during their differentiation and movement in the olfactory epithelium in C. inermis. Staining for F-actin (FITC phalloidin, green) and for nuclei (DAPI, blue); laser confocal microscopy. (A) OSN during migration (3D reconstruction); (b) A dendrite with nuclear material inside (2D section) and its orthogonal projections (b1 and b2); (c) a lengthwise cut through a iOSN; nuclear material is located inside the actin microfilaments; the front section of the dendrite is marked by an arrow; (d) apical surface of the iOSN dendrite that contains a section without actin microfilaments (marked by an arrow); (e) uneven contours of the front section of the dendrite (marked by an arrow), where the growth cone is presumably located. The red arrow indicates the direction to the surface of the olfactory epithelium.