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

. 2021 Jul 30;4:928. doi: 10.1038/s42003-021-02427-0

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

© The Author(s) 2021

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. 3 — a Mice received an intra-peritoneal acetate (Ac) injection (500 mg/kg) followed by analysis of blood acetate concentrations (isolated from the tail vein) and neutrophil phenotypes 30 min and 6 h after injection. b Acetate (Ac) i.p. injection caused a two-fold serum acetate increase 30 min after injection and normal serum acetate levels were restored after 6 h. c Neutrophils isolated from mice treated with acetate showed enhanced complement (CD11b) and Fcγ (CD16/CD32) receptor expression compared to PBS-treated mice. d In vivo acetate (Ac) injection caused increased ROS production upon stimulation with phorbol-12-myristat-13-acetate (PMA). Data in all panels represent geometric means from six animals. *P < 0.05; **P < 0.01 significant difference versus the indicated condition as calculated by Mann–Whitney U test.