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Identification of SLC15A4/PHT1 Gene Products Upregulation Marking the Intestinal Epithelial Monolayer of Ulcerative Colitis Patients

SLC15A4/PHT1 is an endolysosome-resident carrier of oligopeptides and histidine recently come into view as a key path marker of immune/autoimmune/inflammatory pathways in immune cells. Yet, its emerging role in inflammatory processes directly targeting the gastrointestinal epithelial layer, as in th...

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Autores principales: Mazzei, Aurora, Serino, Grazia, Romano, Alessandro, Piccinno, Emanuele, Scalavino, Viviana, Valentini, Anna Maria, Armentano, Raffaele, Schiavone, Roberta, Giannelli, Gianluigi, Verri, Tiziano, Barca, Amilcare
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9658943/
https://www.ncbi.nlm.nih.gov/pubmed/36361959
http://dx.doi.org/10.3390/ijms232113170
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author Mazzei, Aurora
Serino, Grazia
Romano, Alessandro
Piccinno, Emanuele
Scalavino, Viviana
Valentini, Anna Maria
Armentano, Raffaele
Schiavone, Roberta
Giannelli, Gianluigi
Verri, Tiziano
Barca, Amilcare
author_facet Mazzei, Aurora
Serino, Grazia
Romano, Alessandro
Piccinno, Emanuele
Scalavino, Viviana
Valentini, Anna Maria
Armentano, Raffaele
Schiavone, Roberta
Giannelli, Gianluigi
Verri, Tiziano
Barca, Amilcare
author_sort Mazzei, Aurora
collection PubMed
description SLC15A4/PHT1 is an endolysosome-resident carrier of oligopeptides and histidine recently come into view as a key path marker of immune/autoimmune/inflammatory pathways in immune cells. Yet, its emerging role in inflammatory processes directly targeting the gastrointestinal epithelial layer, as in the multifactorial pathophysiology of inflammatory bowel disease (IBD), is poorly investigated. Here, the first identification of SLC15A4/PHT1 gene products in human colonic epithelium of ulcerative colitis (UC) patients is reported, showing protein primarily localized in intracellular vesicle-like compartments. Qualitative and quantitative immunohistochemical analyses of colon biopsies revealed overexpression of SLC15A4/PHT1 protein product in the epithelial layer of UC patients. Results were successfully mirrored in vitro, in spontaneously differentiated enterocyte-like monolayers of Caco-2 cells specifically exposed to DSS (dextran sodium sulphate) to mimic IBD inflammatory onsets. SLC15A4/PHT1 expression and cellular localization were characterized confirming its (dys)regulation traits in inflamed vs. healthy epithelia, strongly hinting the hypothesis of SLC15A4/PHT1 increased function associated with epithelial inflammation in IBD patients.
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spelling pubmed-96589432022-11-15 Identification of SLC15A4/PHT1 Gene Products Upregulation Marking the Intestinal Epithelial Monolayer of Ulcerative Colitis Patients Mazzei, Aurora Serino, Grazia Romano, Alessandro Piccinno, Emanuele Scalavino, Viviana Valentini, Anna Maria Armentano, Raffaele Schiavone, Roberta Giannelli, Gianluigi Verri, Tiziano Barca, Amilcare Int J Mol Sci Article SLC15A4/PHT1 is an endolysosome-resident carrier of oligopeptides and histidine recently come into view as a key path marker of immune/autoimmune/inflammatory pathways in immune cells. Yet, its emerging role in inflammatory processes directly targeting the gastrointestinal epithelial layer, as in the multifactorial pathophysiology of inflammatory bowel disease (IBD), is poorly investigated. Here, the first identification of SLC15A4/PHT1 gene products in human colonic epithelium of ulcerative colitis (UC) patients is reported, showing protein primarily localized in intracellular vesicle-like compartments. Qualitative and quantitative immunohistochemical analyses of colon biopsies revealed overexpression of SLC15A4/PHT1 protein product in the epithelial layer of UC patients. Results were successfully mirrored in vitro, in spontaneously differentiated enterocyte-like monolayers of Caco-2 cells specifically exposed to DSS (dextran sodium sulphate) to mimic IBD inflammatory onsets. SLC15A4/PHT1 expression and cellular localization were characterized confirming its (dys)regulation traits in inflamed vs. healthy epithelia, strongly hinting the hypothesis of SLC15A4/PHT1 increased function associated with epithelial inflammation in IBD patients. MDPI 2022-10-29 /pmc/articles/PMC9658943/ /pubmed/36361959 http://dx.doi.org/10.3390/ijms232113170 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mazzei, Aurora
Serino, Grazia
Romano, Alessandro
Piccinno, Emanuele
Scalavino, Viviana
Valentini, Anna Maria
Armentano, Raffaele
Schiavone, Roberta
Giannelli, Gianluigi
Verri, Tiziano
Barca, Amilcare
Identification of SLC15A4/PHT1 Gene Products Upregulation Marking the Intestinal Epithelial Monolayer of Ulcerative Colitis Patients
title Identification of SLC15A4/PHT1 Gene Products Upregulation Marking the Intestinal Epithelial Monolayer of Ulcerative Colitis Patients
title_full Identification of SLC15A4/PHT1 Gene Products Upregulation Marking the Intestinal Epithelial Monolayer of Ulcerative Colitis Patients
title_fullStr Identification of SLC15A4/PHT1 Gene Products Upregulation Marking the Intestinal Epithelial Monolayer of Ulcerative Colitis Patients
title_full_unstemmed Identification of SLC15A4/PHT1 Gene Products Upregulation Marking the Intestinal Epithelial Monolayer of Ulcerative Colitis Patients
title_short Identification of SLC15A4/PHT1 Gene Products Upregulation Marking the Intestinal Epithelial Monolayer of Ulcerative Colitis Patients
title_sort identification of slc15a4/pht1 gene products upregulation marking the intestinal epithelial monolayer of ulcerative colitis patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9658943/
https://www.ncbi.nlm.nih.gov/pubmed/36361959
http://dx.doi.org/10.3390/ijms232113170
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