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. Author manuscript; available in PMC: 2017 Sep 1.
Published in final edited form as: Neurochem Int. 2016 Jun 6;98:129–137. doi: 10.1016/j.neuint.2016.05.010

Fig. 3. Requirement of SERT expression in TCAs not SERT in cortical neurons for 5-HT uptake in the barrel cortex.

Fig. 3

A. SERT (grayscale) and Vglut2 (green) double immunostaining of coronal sections of somatosensory cortex from P7 mice. Control SERTfl/fl mice displayed two distinct classes of SERT+ fibers: fibers that were relatively thin, smooth and co-labeled with Vglut2+ TCA patches at layer 4 (L4) (strongly) and layer 6 (L6) (weakly), and fibers that were thick, punctated, randomly distributed as shown in enlarged views in third row images. No SERT immunostaining was discernible in SERTNull mice. SERT immunostaining in Vglut2+ patches was not detectable in SERTGluΔ but undiminished in SERTCortexΔ and SERTRapheΔ mice. SERT immunostaining in the thick fibers was dramatically reduced in SERTRapheΔ, but undiminished in SERTGluΔ and SERTCortexΔ mice. B. 5-HT (grayscale) and Vglut2 (green) double immunolabeling of coronal sections of P7 somatosensory cortex. 5-HT immunostaining of Vglut2+ patches but not the thick fibers was dramatically reduced in SERTGluΔ. 5-HT immunostaining of both the thick fibers and Vglut2+ patches in SERTCortexΔ was indistinguishable from that in SERTRapheΔ and control littermate mice. For each brain sample, SERT and Vglut2 double immunostaining (A) and 5-HT and Vglut2 double immunostaining (B) represent adjacent sections. Third row images show an enlarged view of SERT immunohistochemistry (A) or 5-HT immunohistochemistry (B) in areas outlined by red boxes on images in respective second row. Images for SERTNull, SERTRapheΔ and SERTGluΔ cortices are reproduced from our previous study (Chen et al., 2015) for comparison of SERT and 5-HT immunostaining patterns in age-matched SERTCortexΔ mice. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)