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

. 2023 Jan 30;14(1):70. doi: 10.1038/s41419-023-05607-4

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

© The Author(s) 2023

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/.

PMC Copyright notice

Fig. 8 — A Schematic representation of co-culture of PC12 cells and BMDMs. B, E Representative western blots of Cleaved Caspase-3 and Bcl-2 in PC12 cells. Quantitative analysis of the Cleaved Caspase-3/GAPDH ratio and Bcl-2/GAPDH ratio in PC12 cells (n = 3). C, F Flow cytometry assay detected apoptosis of PC12 cells in each group, showing that SCDEs inhibited LPS-induced apoptosis and that the knockout of MFG-E8 reversed the positive effect (n = 3). D, G The TUNEL staining of PC12 cells showed that SCDEs reduced TUNEL + cells while MFG-E8 knockout increased TUNEL + cells (n = 3). Scale bar: 50 μm. Data were presented as mean ± SEM. Results were analyzed by One-way ANOVA. Significance: ns-not significant, *P < 0.05, **P < 0.01, ***P < 0.001.