Abstract
For several years, it was believed that the thymus was entirely responsible for maintaining T cell homeostasis. Today, it is well-known that homeostatic peripheral mechanisms are essential in order to maintain T cell numbers and diversity constant in the periphery. Naïve and memory T cells require continual access to self-peptide MHC class I and II molecules and/or cytokines to survive in the periphery. Under normal conditions, homeostatic resources are low, and lymphocytes undergo very slow proliferation and survive. Following T cell depletion, the bioavailability of homeostatic resources is significantly increased, and T cell proliferation is dramatically augmented. The development of lymphopenic mouse models has helped our current understanding of factors involved in the regulation of peripheral T cell homeostasis. In this minireview, we will give a brief overview about basic techniques used to study peripheral T cell homeostasis in mice.
Key words
- Lymphopenia
- Homeostasis
- Lymphocytes
- CD4
- CD8
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Acknowledgments
This work was supported by grants from the Cancer Research Society of Canada (grant no. 22669 and 24380 to M.G.) and in part by a grant from the Foundation de l’Hôpital Maisonneuve-Rosemont, Montreal, Quebec, Canada.
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Moutuou, M.M., Gauthier, SD., Chen, N., Leboeuf, D., Guimond, M. (2020). Studying Peripheral T Cell Homeostasis in Mice: A Concise Technical Review. In: Liu, C. (eds) T-Cell Receptor Signaling. Methods in Molecular Biology, vol 2111. Humana, New York, NY. https://doi.org/10.1007/978-1-0716-0266-9_21
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DOI: https://doi.org/10.1007/978-1-0716-0266-9_21
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