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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorFortea, Marina
dc.contributor.authorHacour, Leen
dc.contributor.authorSancho, Francesc J.
dc.contributor.authorBoada, Carlos
dc.contributor.authorSevillano-Aguilera, Cesar
dc.contributor.authorSalvo Romero, Eloisa
dc.contributor.authorLobo Alvarez, Beatriz
dc.contributor.authorVicario Perez, Maria
dc.contributor.authorGonzález Castro, Ana Maria
dc.contributor.authorGuagnozzi, Danila
dc.contributor.authorAlonso Cotoner, Carmen
dc.contributor.authorSantos, Javier
dc.date.accessioned2024-11-21T13:57:37Z
dc.date.available2024-11-21T13:57:37Z
dc.date.issued2024-09
dc.identifier.citationFortea M, Hacour L, Sancho F, Boada C, Sevillano-Aguilera C, González-Castro AM, et al. Characterization of Immune Cell Populations and Acid-Sensing Receptors in the Human Esophagus. Gastroenterol Insights. 2024 Sep:15(3):819–34.
dc.identifier.issn2036-7422
dc.identifier.urihttps://hdl.handle.net/11351/12254
dc.descriptionImmune cell; Acid; Human esophagus
dc.description.abstractIntroduction: Esophageal inflammatory diseases are frequent diagnoses in clinical practice and have diverse etiologies, the most common being those associated with the exposure to gastric content, drugs and allergens. In diseases, the immunological component is well identified in endoscopic biopsies, which mainly contain the epithelium and the lamina propria; however, deeper layers are less studied. Moreover, the esophageal capacity of sensing luminal compounds is poorly understood. Methods: In transmural sections from proximal, middle and distal esophagus obtained from deceased patients, we performed a phenotypic analysis of the main immune cell populations and acid-sensing receptors by immunohistochemistry and immunofluorescence methods. Results: A total of nine donors were studied (absence of pathology, optimal tissue preservation and orientation). We found the following: (1) the vascular papillae and the lamina propria are the most infiltrated layers by the lymphoid lineage (T and B lymphocytes), followed by the epithelium, while the smooth muscular layers are mainly populated by the myeloid lineage (macrophages and mast cells); (2) intraepithelial macrophages are consistently found along the esophagus; and (3) eosinophils are absent in all the esophageal layers. The acid-sensing receptors ASIC-1, ASIC-2 and δENAC are expressed in the esophageal epithelium and in the lamina propria, yet only ASIC-2 is expressed in the muscularis mucosae. Conclusions: The human esophagus contains a differential distribution of immune cells and acid-sensing receptors across its layers. This study extends the esophageal histological knowledge previously described and reinforces its role as a defensive and sensing organ.
dc.language.isoeng
dc.publisherMDPI
dc.relation.ispartofseriesGastroenterology Insights;15(3)
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectÀcid gàstric
dc.subjectFenotip
dc.subjectEsòfag - Efecte dels medicaments
dc.subjectImmunohistoquímica
dc.subjectIntestins - Inflamació
dc.subject.meshEsophagus
dc.subject.mesh/drug effects
dc.subject.meshGastric Acid
dc.subject.meshImmunohistochemistry
dc.subject.meshPhenotype
dc.subject.meshInflammatory Bowel Diseases
dc.titleCharacterization of Immune Cell Populations and Acid-Sensing Receptors in the Human Esophagus
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3390/gastroent15030058
dc.subject.decsesófago
dc.subject.decs/efectos de los fármacos
dc.subject.decsácido gástrico
dc.subject.decsinmunohistoquímica
dc.subject.decsfenotipo
dc.subject.decsenfermedad inflamatoria intestinal
dc.relation.publishversionhttps://doi.org/10.3390/gastroent15030058
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Fortea M, Boada C, Sevillano-Aguilera C, Salvo-Romero E, Guagnozzi D] Grup de Recerca d’Immunologia Translacional, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. [Hacour L] Translational Research Center for Gastrointestinal Disorders (TARGID), Deparment of Chronic Diseases and Metabolism, Leuven, Belgium. [Sancho F] Department of Pathology, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain. [González-Castro AM, Vicario M] Grup de Recerca d’Immunologia Translacional, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Instituto de Salud Carlos III, Madrid, Spain. [Lobo B, Alonso-Cotoner C, Santos J] Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Instituto de Salud Carlos III, Madrid, Spain. Grup de Recerca de Fisiologia i Fisiopatologia Digestiva, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain
dc.identifier.wos001323449400001
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PE2013-2016/PI16%2F00583
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PE2017-2020/PI19%2F01643
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/1PN/2008-2011%2FCM08%2F00229
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PE2017-2020/PI19%2F01643
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PE2013-2016/FI12%2F00254
dc.relation.projectidinfo:eu-repo/grantAgreement/ES/PE2013-2016/PI15%2F00301
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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