Significance of PD1 Alternative Splicing in Celiac Disease as a Novel Source for Diagnostic and Therapeutic Target

BackgroundWe have focused on the alteration of the PD-1/PD-L1 pathway in celiac disease and discussed the roles of the PD1 pathway in regulating the immune response. We explored the idea that the altered mRNA splicing process in key regulatory proteins could represent a novel source to identify diag...

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Main Authors: Candelaria Ponce de León, Pedro Lorite, Miguel Ángel López-Casado, Francisco Barro, Teresa Palomeque, María Isabel Torres
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-06-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2021.678400/full
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spelling doaj-6dee7a3cc9424d4b8ab00684e208b2722021-06-16T10:03:57ZengFrontiers Media S.A.Frontiers in Immunology1664-32242021-06-011210.3389/fimmu.2021.678400678400Significance of PD1 Alternative Splicing in Celiac Disease as a Novel Source for Diagnostic and Therapeutic TargetCandelaria Ponce de León0Pedro Lorite1Miguel Ángel López-Casado2Francisco Barro3Teresa Palomeque4María Isabel Torres5Department of Experimental Biology, Faculty of Health Sciences, University of Jaén, Jaén, SpainDepartment of Experimental Biology, Faculty of Health Sciences, University of Jaén, Jaén, SpainDepartment of Pediatric Gastroenterology, Virgen de las Nieves Hospital, Granada, SpainDepartment of Plant Genetic Improvement, Institute for Sustainable Agriculture, Spanish National Research Council (CSIC), Córdoba, SpainDepartment of Experimental Biology, Faculty of Health Sciences, University of Jaén, Jaén, SpainDepartment of Experimental Biology, Faculty of Health Sciences, University of Jaén, Jaén, SpainBackgroundWe have focused on the alteration of the PD-1/PD-L1 pathway in celiac disease and discussed the roles of the PD1 pathway in regulating the immune response. We explored the idea that the altered mRNA splicing process in key regulatory proteins could represent a novel source to identify diagnostic, prognostic, and therapeutic targets in celiac disease.MethodsWe characterized the PD1 mRNA variants’ profile in CD patients and in response to gluten peptides’ incubation after in vitro experiments. Total RNA from whole blood was isolated, and the coding region of the human PD-1 mRNA was amplified by cDNA PCR.ResultsPCR amplification of the human PD-1 coding sequence revealed an association between the over-expression of the sPD-1 protein and the PD-1Δex3 transcript in celiac disease. Thus, we have found three novel alternative spliced isoforms, two of which result in a truncated protein and the other isoform with a loss of 14 aa of exon 2 and complete exon 3 (Δ3) which could encode a new soluble form of PD1 (sPD-1).ConclusionsOur study provides evidence that dietary gluten can modulate processes required for cell homeostasis through the splicing of pre-mRNAs encoding key regulatory proteins, which represents an adaptive mechanism in response to different nutritional conditions.https://www.frontiersin.org/articles/10.3389/fimmu.2021.678400/fullPD1/PDLceliac diseasealternative splicinggluten peptidesimmune checkpoint
collection DOAJ
language English
format Article
sources DOAJ
author Candelaria Ponce de León
Pedro Lorite
Miguel Ángel López-Casado
Francisco Barro
Teresa Palomeque
María Isabel Torres
spellingShingle Candelaria Ponce de León
Pedro Lorite
Miguel Ángel López-Casado
Francisco Barro
Teresa Palomeque
María Isabel Torres
Significance of PD1 Alternative Splicing in Celiac Disease as a Novel Source for Diagnostic and Therapeutic Target
Frontiers in Immunology
PD1/PDL
celiac disease
alternative splicing
gluten peptides
immune checkpoint
author_facet Candelaria Ponce de León
Pedro Lorite
Miguel Ángel López-Casado
Francisco Barro
Teresa Palomeque
María Isabel Torres
author_sort Candelaria Ponce de León
title Significance of PD1 Alternative Splicing in Celiac Disease as a Novel Source for Diagnostic and Therapeutic Target
title_short Significance of PD1 Alternative Splicing in Celiac Disease as a Novel Source for Diagnostic and Therapeutic Target
title_full Significance of PD1 Alternative Splicing in Celiac Disease as a Novel Source for Diagnostic and Therapeutic Target
title_fullStr Significance of PD1 Alternative Splicing in Celiac Disease as a Novel Source for Diagnostic and Therapeutic Target
title_full_unstemmed Significance of PD1 Alternative Splicing in Celiac Disease as a Novel Source for Diagnostic and Therapeutic Target
title_sort significance of pd1 alternative splicing in celiac disease as a novel source for diagnostic and therapeutic target
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2021-06-01
description BackgroundWe have focused on the alteration of the PD-1/PD-L1 pathway in celiac disease and discussed the roles of the PD1 pathway in regulating the immune response. We explored the idea that the altered mRNA splicing process in key regulatory proteins could represent a novel source to identify diagnostic, prognostic, and therapeutic targets in celiac disease.MethodsWe characterized the PD1 mRNA variants’ profile in CD patients and in response to gluten peptides’ incubation after in vitro experiments. Total RNA from whole blood was isolated, and the coding region of the human PD-1 mRNA was amplified by cDNA PCR.ResultsPCR amplification of the human PD-1 coding sequence revealed an association between the over-expression of the sPD-1 protein and the PD-1Δex3 transcript in celiac disease. Thus, we have found three novel alternative spliced isoforms, two of which result in a truncated protein and the other isoform with a loss of 14 aa of exon 2 and complete exon 3 (Δ3) which could encode a new soluble form of PD1 (sPD-1).ConclusionsOur study provides evidence that dietary gluten can modulate processes required for cell homeostasis through the splicing of pre-mRNAs encoding key regulatory proteins, which represents an adaptive mechanism in response to different nutritional conditions.
topic PD1/PDL
celiac disease
alternative splicing
gluten peptides
immune checkpoint
url https://www.frontiersin.org/articles/10.3389/fimmu.2021.678400/full
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