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Autophagy-dependent regulation of MHC-I molecule presentation.
- Source :
-
Journal of cellular biochemistry [J Cell Biochem] 2024 Nov; Vol. 125 (11), pp. e30416. Date of Electronic Publication: 2023 May 01. - Publication Year :
- 2024
-
Abstract
- The major histocompatibility complex (MHC) class I molecules present peptide antigens to MHC class I-restricted CD8+ T lymphocytes to elicit an effective immune response. The conventional antigen-processing pathway for MHC-I presentation depends on proteasome-mediated peptide generation and peptide loading in the endoplasmic reticulum by members of the peptide loading complex. Recent discoveries in this field highlight the role of alternative MHC-I peptide loading and presentation pathways, one of them being autophagy. Autophagy is a cell-intrinsic degradative pathway that ensures cellular homoeostasis and plays critical roles in cellular immunity. In this review article, we discuss the role of autophagy in MHC class I-restricted antigen presentation, elucidating new findings on the crosstalk of autophagy and ER-mediated MHC-I peptide presentation, dendritic cell-mediated cross-presentation and also mechanisms governing immune evasion. A detailed molecular understanding of the key drivers of autophagy-mediated MHC-I modulation holds promising targets to devise effective measures to improve T cell immunotherapies.<br /> (© 2023 The Authors. Journal of Cellular Biochemistry published by Wiley Periodicals LLC.)
- Subjects :
- Humans
Animals
Dendritic Cells immunology
Dendritic Cells metabolism
CD8-Positive T-Lymphocytes immunology
CD8-Positive T-Lymphocytes metabolism
Endoplasmic Reticulum metabolism
Cross-Priming immunology
Autophagy
Histocompatibility Antigens Class I metabolism
Histocompatibility Antigens Class I immunology
Antigen Presentation immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4644
- Volume :
- 125
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Journal of cellular biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 37126231
- Full Text :
- https://doi.org/10.1002/jcb.30416