Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2020 Dec 14;15:10113–10125. doi: 10.2147/IJN.S282985

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© 2020 Luo et al.

This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).

PMC Copyright notice

Histomorphological changes at 8 weeks post-injury in vivo. (A) Images of spinal cord tissue after staining with H&E, shown at 2X (left, scale bar = 500 μm) and 20 X magniﬁcation (right, scale bar = 50 μm). The images on the right are the corresponding enlarged views of the areas indicated by blue squares in the left images. The red lines indicate the edge of the lesion sites. (B) LFB staining of myelin sheaths is shown at 2X (left, scale bar = 500 μm) and 20X magniﬁcation (right, scale bar = 50 μm). The images on the right are the corresponding enlarged views of the areas indicated by blue squares in the left images. The red lines indicate the edge of the lesion sites. (C) Representative TEM images showing the ultrastructure of myelin sheaths in different groups. Scale bar = 5 μm. (D) Double-staining of the slices with anti-NF200 and anti-NeuN antibodies. Scale bar = 50 μm. (E) Quantitative analysis of mean ﬂuorescence intensity of NF200 staining in Figure 4D, * P< 0.05, in comparison with saline group. (F) Quantitative analysis of mean ﬂuorescence intensity of NeuN staining in Figure 4D. * P < 0.05 and ** P < 0.01, in comparison with saline group.