Diversity of γδ T-cell receptors on murine intestinal intraepithelial lymphocytes
Abstract
The search for the genes encoding the T-cell receptor (TCR) alpha- and beta-subunits revealed a third gene gamma which shares with the alpha- and beta-genes several properties including somatic rearrangement. This gene, together with a fourth rearranging gene delta, encodes a second type of T-cell receptor, TCR gamma delta. Although TCR gamma delta-bearing T cells constitute a relatively minor subpopulation in the thymus and in peripheral lymphoid organs, they are the major lymphocytes of epidermis (dendritic epidermal cells or DEC) and of intestinal epithelium (intestinal intraepithelial lymphocytes or IEL) in mice, suggesting that at least some gamma delta T cells are important in the surveillance of a variety of epithelia. It was recently reported, however, that the TCR gamma delta on DEC has essentially no structural diversity, implying that the putative ligand is monomorphic. As this finding, if generally applicable, poses severe restrictions on the origin of the ligand, we investigated the diversity of the TCR on the second major epithelium-associated gamma delta T cells, namely IEL from mice. We report here that by contrast with the DEC gamma delta, the IEL gamma delta TCR are structurally diverse.
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Vγ3+ thymocytes are generated only during the early fetal stages of thymic development from E13 to E18 and migrate to the epidermis, where a defined homeostatic density is maintained throughout life by self-renewal.
“Vγ3+ thymocytes are generated only during the early fetal stages of thymic development from E13 to E18 and migrate to the epidermis, where a defined homeostatic density is maintained throughout life by self-renewal (30).”
From Comparing Mouse and Human Tissue-Resident γδ T Cells (2022) · cites this paper as [30]
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Haas, J. D., Ravens, S., Düber, S., Sandrock, I., Oberdörfer, L., Kashani, E., Chennupati, V., Föhse, L., Naumann, R., Weiss, S., et al. (2012) · Immunity · doi:10.1016/j.immuni.2012.06.003 · Cited by 348 · see citing works
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HELGELAND, L., VAAGE, J. T., ROLSTAD, B., MIDTVEDT, T., & BRANDTZAEG, P. (1996) · Immunology · doi:10.1046/j.1365-2567.1996.d01-783.x · Cited by 122 · see citing works
Comparing Mouse and Human Tissue-Resident γδ T Cells
Qu, G., Wang, S., Zhou, Z., Jiang, D., Liao, A., & Luo, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.891687 · Cited by 87 · see citing works
“Vg3 thymocytes are generated only during the early fetal stages of thymic development from E13 to E18 and migrate to the epidermis, where a defined homeostatic density is maintained throughout life by self-renewal (30).”
BackgroundMechanisms of activation of innate-like intraepithelial T lymphocytes
Vandereyken, M., James, O. J., & Swamy, M. (2020) · Mucosal Immunology · doi:10.1038/s41385-020-0294-6 · Cited by 65 · see citing works
- Authors
- Takagaki, Y., DeCloux, A., Bonneville, M., & Tonegawa, S.
- Affiliations
- Howard Hughes Medical Institute (US)
- Venue
- Nature
- Published
- 1989-06
- Volume
- 339
- Issue
- 6227
- Pages
- 712-714
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2043462667
- Cited by
- 217
- References
- 0
- Citations by year
- 2026: 3 · 2024: 3 · 2023: 2 · 2022: 4 · 2020: 5 · 2019: 1 · 2018: 1 · 2017: 4 · 2015: 1 · 2014: 2 · 2013: 1 · 2012: 3
- FWCI
- 12.76
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Monoclonal and Polyclonal Antibodies Research
- Keywords
- γδ T cells, T cell receptor diversity, intestinal intraepithelial lymphocytes, somatic rearrangements, dendritic epidermal T cells, T cell receptor ligands
- MeSH terms
- Animals, Base Sequence, Epithelial Cells, Intestines, Mice, Inbred C57BL, Molecular Sequence Data, Receptors, Antigen, T-Cell, T-Lymphocytes, Transcription, Genetic, Gene Rearrangement, T-Lymphocyte, Gene Rearrangement, gamma-Chain T-Cell Antigen Receptor, Macromolecular Substances, Mice
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