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

. 2019 Sep 2;9:12645. doi: 10.1038/s41598-019-49164-3

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

© The Author(s) 2019

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

Flow cytometry analysis of immunoinfiltrates in colons. Epithelial (EP) and LP leukocyte population were isolated from colon samples as described in Materials and Methods section. (A) Myeloid population was investigated using panel 1 and cells were immunophenotyped as follow: macrophages as CD11b+/F4/80+; moncytes as CD11b+/F4/80−/Ly6C+; granulocytes as CD11b+/F4/80−/Ly6G+, dendritic cells as F4/80^int/CD11c^Hi. (B) Lymphoid population was characterized using panel 2 and immunophenotyped as follow: T lymphocytes as CD11b−/CD3+/CD19−; B lymphocytes as CD11b−/CD3−/CD19+. (C) T lymphocytes were immunophenotyped on the basis of CD4+ or CD8+ gates. Bar graphs show mean values ± s.d. from at least three mice individually tested per group.