Sep 22, 2021
MAIT Cell Expansion in Donor Mice
- Timothy S C Hinks1,
- Bonnie van Wilgenburg2,
- Huimeng Wang3,
- Liyen Loh3,
- Marios Koutsakos3,
- Katherine Kedzierska3,
- Alexandra J. Corbett3,
- Zhenjun Chen3
- 1Respiratory Medicine Unit, Nuffield Department of Medicine Experimental Medicine, University of Oxford, Oxfordshire, UK;
- 2Peter Medawar Building for Pathogen Research and Translational Gastroenterology Unit, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK;
- 3Department of Microbiology and Immunology, The Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Parkville, Australia
- Springer Nature Books
Protocol Citation: Timothy S C Hinks, Bonnie van Wilgenburg, Huimeng Wang, Liyen Loh, Marios Koutsakos, Katherine Kedzierska, Alexandra J. Corbett, Zhenjun Chen 2021. MAIT Cell Expansion in Donor Mice. protocols.io https://dx.doi.org/10.17504/protocols.io.bmeqk3dw
Manuscript citation:
Hinks T.S.C. et al. (2020) Study of MAIT Cell Activation in Viral Infections In Vivo. In: Kaipe H., Magalhaes I. (eds) MAIT Cells. Methods in Molecular Biology, vol 2098. Humana, New York, NY. https://doi.org/10.1007/978-1-0716-0207-2_17
License: This is an open access protocol distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
Created: September 16, 2020
Last Modified: September 22, 2021
Protocol Integer ID: 42160
Keywords: Virus, MAIT cell, Flow cytometry, MR1-tetramer, Infection, Mouse ,
Abstract
This is part 3.1 of the "Study of MAIT Cell Activation in Viral Infections In Vivo" collection of protocols.
Collection Abstract: MAIT cells are abundant, highly evolutionarily conserved innate-like lymphocytes expressing a semi-invariant T cell receptor (TCR), which recognizes microbially derived small intermediate molecules from the riboflavin biosynthetic pathway. However, in addition to their TCR-mediated functions they can also be activated in a TCR-independent manner via cytokines including IL-12, -15, -18, and type I interferon. Emerging data suggest that they are expanded and activated by a range of viral infections, and significantly that they can contribute to a protective anti-viral response. Here we describe methods used to investigate these anti-viral functions in vivo in murine models. To overcome the technical challenge that MAIT cells are rare in specific pathogen-free laboratory mice, we describe how pulmonary MAIT cells can be expanded using intranasal bacterial infection or a combination of synthetic MAIT cell antigen and TLR agonists. We also describe protocols for adoptive transfer of MAIT cells, methods for lung homogenization for plaque assays, and surface and intracellular cytokine staining to determine MAIT cell activation.
Abstract: MAIT cells are rare in specific pathogen-free mice [6], typically comprising about 1 x 104 recoverable pulmonary MAIT cells in an infection-naive adult C57BL/6 mouse. Therefore, for adoptive transfer experiments, the MAIT cell population should first be expanded using intranasal infection [15] or immunization (5-OP-RU with TLR agonists) [3, 15] (see Note 5). When planning the adoptive transfer experiment, estimate that one S. Typhimurium BRD509-infected mouse will yield 1–2 x 106 sorted MAITcells, which are enough for 10–20 recipient mice (105 MAIT cells/RAG2–/–γC–/– mouse in this case). Infect donor mice 7 days earlier than the adoptive transfer.
Attachments
Materials
For materials, please refer to the Guidelines section of the '"Study of MAIT Cell Activation in Viral Infections In Vivo" collection.
Safety warnings
Personal protective equipment (PPE) should be worn at all times (gloves, lab coat, & eye protection) (see Notes 3 and 4).
For hazard information and safety warnings, please refer to the SDS (Safety Data Sheet).
Two days before infection streak out a plate of S. Typhimurium BRD509 (an attenuated vaccine strain [14]) on LB agar plates, containing 50 μg/ml streptomycin and incubate plates Overnight at 37 °C .
The day before infection, pick a single colony under flame and inoculate to 10 mL LB culture medium with 50 μg/ml streptomycin and leave static at 37 °C (double contained if working with wild type/virulent SL1344 or equivalent strains) Overnight .
On the day of infection, re-inoculate into fresh 10 mL pre-warmed LB culture medium with 0.5 µL , 100 µL , or 20 µL of overnight culture, under flame. This is to ensure an optimal optical density (O.D.) reading (bacteria in log phase growth) for preparing the inoculum later (see Note 6). The doublingtime for Salmonella can vary between 0.5 and 1 h. Make the infection inoculum from culture with O.D.600nm reading between 0.2 and 0.6. Calculate the required CFU of bacteria estimating 1 O.D. = 5–10 × 108 CFU (this constant needs to be established for individual labs). Dilute with PBS to a final concentration of 2 x 107 CFU/mL, allowing 50 μL inoculum/mouse, i.e., 106 CFU/50 μL/mouse.
Infect mice i.n. with 106 CFU S. Typhimurium BRD509 in 50 µL PBS under isoflurane anesthesia (see Notes 7 and 8).
Allow mice to recover and monitor mice for 7 days to allow the infection to take its course and MAIT cell frequencies to expand dramatically from 104 to 5 × 106 MAIT cells, or from 1 % to 20 % –50 % of all alpha-beta T cells [15] (see Note 8).