| Literature DB >> 33479908 |
Akihiko Oka1,2, Bo Liu1, Jeremy W Herzog1, R Balfour Sartor3,4,5.
Abstract
Although the inflammatory cytokine IL-10 is pivotal in regulatory B-cell function, detecting IL-10-producing B cells by intracellular IL-10 staining requires multiple steps and tedious preparation. In contrast, the Il10-eGFP reporter mouse model (VertX), generated in 2009, allows easier and quicker detection of IL-10-producing B cells with the possibility of sorting viable cells without membrane permeabilization and ex vivo activation. Even though detecting IL-10+ cells is simpler, several nuances are important. For example, methanol-containing buffers delete GFP signal, while long-term fixation can maintain GFP intensity but decreases other intracellular signals (FOXP3, etc.). Here, we provide optimized and improved protocols for GFP detection in intestinal B cells and isolation techniques of lamina propria, spleen, mesenteric lymph node, peritoneum, and blood cells from VertX mice.Entities:
Keywords: Flow cytometry; GFP; Gnotobiotic mice; Interleukin-10; Microbiota; Mucosal immunology; Regulatory B cell
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Year: 2021 PMID: 33479908 DOI: 10.1007/978-1-0716-1237-8_19
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745