Epithelial recognition and elimination against aberrant cells
- PMID: 38411739
- DOI: 10.1007/s00281-024-01001-0
Epithelial recognition and elimination against aberrant cells
Erratum in
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Publisher Correction: Epithelial recognition and elimination against aberrant cells.Semin Immunopathol. 2024 Jan;45(4-6):551-554. doi: 10.1007/s00281-024-01009-6. Semin Immunopathol. 2024. PMID: 38656341 No abstract available.
Abstract
Epithelial cells, which are non-immune cells, not only function as a physical defence barrier but also continuously monitor and eliminate aberrant epithelial cells in their vicinity. In other words, it has become evident that epithelial cells possess immune cell-like functions. In fact, recent research has revealed that epithelial cells recognise the Major Histocompatibility Complex I (MHC-I) of aberrant cells as a mechanism for surveillance. This cellular defence mechanism of epithelial cells probably detects aberrant cells more promptly than the conventional immune response, making it a novel and primary biological defence. Furthermore, there is the potential for this new immune-like biological defence mechanism to establish innovative treatment for disease prevention, leading to increasing anticipation for its future medical applications. In this review, we aim to summarise the recognition and attack mechanisms of aberrant cells by epithelial cells in mammals, with a particular focus on the field of cancer. Additionally, we discuss the potential therapeutic applications of epithelial cell-based defence against cancer, including novel prophylactic treatment methods based on molecular mechanisms.
Keywords: Anti-carcinogenesis; Epithelial surveillance; Immune cell-like function; MHC-I.
© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
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References
-
- Morata G, Ripoll P (1975) Minutes — mutants of Drosophila autonomously affecting cell-division rate. Dev Biol 42(2):211–221. https://doi.org/10.1016/0012-1606(75)90330-9 - DOI - PubMed
-
- Van Neerven SM, Vermeulen L (2023) Cell competition in development, homeostasis and cancer. Nat Rev Mol Cell Biol 24(3):221–236. https://doi.org/10.1038/s41580-022-00538-y - DOI - PubMed
-
- Maruyama T, Fujita Y (2017) Cell competition in mammals — novel homeostatic machinery for embryonic development and cancer prevention. Curr Opin Cell Biol 48:106–112. https://doi.org/10.1016/j.ceb.2017.06.007 - DOI - PubMed
-
- Maruyama T, Fujita Y (2022) Cell competition in vertebrates—a key machinery for tissue homeostasis. Curr Opin Genet Dev 72:15–21. https://doi.org/10.1016/j.gde.2021.09.006 - DOI - PubMed
-
- Hogan C, Dupré-Crochet S, Norman M et al (2009) Characterization of the interface between normal and transformed epithelial cells. Nat Cell Biol 11(4):460–467. https://doi.org/10.1038/ncb1853 - DOI - PubMed
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