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. 2017 Oct 24;7:13915. doi: 10.1038/s41598-017-14246-7

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© The Author(s) 2017

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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Dorsal root ganglion of a Beagle dog (a,d,g), a C57BL/6 mouse (b,e,h), and a gray langur (Semnopithecus sp.) (c,f,i). (a–c) Glial fibrillary acidic protein (GFAP), 2′,3′-cyclic-nucleotide 3′-phosphodiesterase (CNPase) (d–f), and (g–i) glutamine synthetase (GS). Most satellite glial cells (SGCs) are immunopositive for GFAP and CNPase in dogs and monkeys, whereas most murine SGCs lack expression of these markers (arrowheads). Note single CNPase⁺ SGC (arrow, e). In contrast, GS represents a good marker for murine and simian SGCs but not for canine SGCs. There are SGCs positive (arrow) and negative for GS (arrowhead) in dogs. Immunohistochemistry using the avidin-biotin-peroxidase complex method, the chromogen 3,3′-diamino-benzidine, and Mayer’s hematoxylin as counterstain. Bars, 40 μm.