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 Mar 19;11:6428. doi: 10.1038/s41598-021-85760-y

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 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/.

PMC Copyright notice

Circulatory levels of adipose tissue macrophage (ATM) markers in the steady state of obese type 2 diabetes (OT2D). Plasma level of MCP-1 (A), MIF (B) and netrin-1 (C) in control subjects (black circles) and obese subjects with T2D (blue circles). Basal level of plasma MCP-1 did not alter in OT2D compared to control (698 ± 49 vs 760 ± 73 RFU of MCP-1, OT2D vs control, p = ns). Basal level of plasma MIF and netrin-1was increased in OT2D (1387 ± 223 vs 1007 ± 29 RFU of MIF-1 and 558 ± 30 vs 478 ± 19 RFU of netrin-1, OT2D vs control, p < 0.05). Acute normalization of glycemia had no effect on levels of LBP, CD80 or CD38 in T2D subjects (A-C). Data were presented as mean ± SEM. *, p < 0.05.