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

. 2024 Jul 6;15:199. doi: 10.1186/s13287-024-03817-x

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

© The Author(s) 2024

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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

PMC Copyright notice

Fig. 1 — Comparison of the characteristics of ex vivo-expanded NG2/_BMMSCs and parental_BMMSCs. (Aa-c) Comparison of the sizes of m-NG2/_BMMSCs (a) and parental m-_BMMSCs (b) and quantification (c, n = 20). (B) FCM analyses and IF staining (red) of NG-2⁺ cells (arrow) in mouse marrow MSC (m-_BMMSC) cultures; n = 6/type of experiment. (C) Measurement of the purity of the isolated and ex vivo-expanded NG2⁺ cells using FCM (left panel) and IF staining (green, arrow); n = 3/method. (D) NG2⁺ cells (boxes) within m-_BMMSC cultures generated smaller spindle-shaped _BMMSCs (thin arrows, S1 and S2 represent individual cultures. (Ea, b) IF staining for SSEA-3 in m-NG2/_BMMSCs (a, red) and m-_BMMSCs (b, green) and quantification from a and b. (F, boxes), n = 3. The means ± SDs of duplicate preparations from three independent experiments are shown. Scale bars = 200 μm for all the images except for those in A and D; scale bars = 100 μm. ** ##p < 0.001 compared with m-_BMMSCs