Broad MICA/B Expression in the Small Bowel Mucosa: A Link between Cellular Stress and Celiac Disease

The MICA/B genes (MHC class I chain related genes A and B) encode for non conventional class I HLA molecules which have no role in antigen presentation. MICA/B are up-regulated by different stress conditions such as heat-shock, oxidative stress, neoplasic transformation and viral infection. Particul...

Descripción completa

Guardado en:
Detalles Bibliográficos
Publicado: 2013
Materias:
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_19326203_v8_n9_p_Allegretti
http://hdl.handle.net/20.500.12110/paper_19326203_v8_n9_p_Allegretti
Aporte de:
id paper:paper_19326203_v8_n9_p_Allegretti
record_format dspace
spelling paper:paper_19326203_v8_n9_p_Allegretti2023-06-08T16:31:18Z Broad MICA/B Expression in the Small Bowel Mucosa: A Link between Cellular Stress and Celiac Disease CD20 antigen CD3 antigen CD68 antigen CD7 antigen glycoprotein p 15095 major histocompatibility antigen class 1 major histocompatibility antigen class 2 syndecan 1 article B lymphocyte celiac disease cell stress cellular distribution child clinical article confocal microscopy controlled study disease severity endoplasmic reticulum stress flow cytometry gene gene expression regulation human human cell human tissue immune dysregulation immunofluorescence test immunopathogenesis intestine biopsy lamina propria macrophage MICA gene MICAB gene oxidative stress preschool child protein localization small intestine mucosa B-Lymphocytes Celiac Disease Child, Preschool Duodenum Enterocytes Female Gene Expression Histocompatibility Antigens Class I Humans Intestinal Mucosa Macrophages Male Plasma Cells Severity of Illness Index Stress, Physiological T-Lymphocytes The MICA/B genes (MHC class I chain related genes A and B) encode for non conventional class I HLA molecules which have no role in antigen presentation. MICA/B are up-regulated by different stress conditions such as heat-shock, oxidative stress, neoplasic transformation and viral infection. Particularly, MICA/B are expressed in enterocytes where they can mediate enterocyte apoptosis when recognised by the activating NKG2D receptor present on intraepithelial lymphocytes. This mechanism was suggested to play a major pathogenic role in active celiac disease (CD). Due to the importance of MICA/B in CD pathogenesis we studied their expression in duodenal tissue from CD patients. By immunofluorescence confocal microscopy and flow cytometry we established that MICA/B was mainly intracellularly located in enterocytes. In addition, we identified MICA/B+ T cells in both the intraepithelial and lamina propria compartments. We also found MICA/B+ B cells, plasma cells and some macrophages in the lamina propria. The pattern of MICA/B staining in mucosal tissue in severe enteropathy was similar to that found in in vitro models of cellular stress. In such models, MICA/B were located in stress granules that are associated to the oxidative and ER stress response observed in active CD enteropathy. Our results suggest that expression of MICA/B in the intestinal mucosa of CD patients is linked to disregulation of mucosa homeostasis in which the stress response plays an active role. © 2013 Allegretti et al. 2013 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_19326203_v8_n9_p_Allegretti http://hdl.handle.net/20.500.12110/paper_19326203_v8_n9_p_Allegretti
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic CD20 antigen
CD3 antigen
CD68 antigen
CD7 antigen
glycoprotein p 15095
major histocompatibility antigen class 1
major histocompatibility antigen class 2
syndecan 1
article
B lymphocyte
celiac disease
cell stress
cellular distribution
child
clinical article
confocal microscopy
controlled study
disease severity
endoplasmic reticulum stress
flow cytometry
gene
gene expression regulation
human
human cell
human tissue
immune dysregulation
immunofluorescence test
immunopathogenesis
intestine biopsy
lamina propria
macrophage
MICA gene
MICAB gene
oxidative stress
preschool child
protein localization
small intestine mucosa
B-Lymphocytes
Celiac Disease
Child, Preschool
Duodenum
Enterocytes
Female
Gene Expression
Histocompatibility Antigens Class I
Humans
Intestinal Mucosa
Macrophages
Male
Plasma Cells
Severity of Illness Index
Stress, Physiological
T-Lymphocytes
spellingShingle CD20 antigen
CD3 antigen
CD68 antigen
CD7 antigen
glycoprotein p 15095
major histocompatibility antigen class 1
major histocompatibility antigen class 2
syndecan 1
article
B lymphocyte
celiac disease
cell stress
cellular distribution
child
clinical article
confocal microscopy
controlled study
disease severity
endoplasmic reticulum stress
flow cytometry
gene
gene expression regulation
human
human cell
human tissue
immune dysregulation
immunofluorescence test
immunopathogenesis
intestine biopsy
lamina propria
macrophage
MICA gene
MICAB gene
oxidative stress
preschool child
protein localization
small intestine mucosa
B-Lymphocytes
Celiac Disease
Child, Preschool
Duodenum
Enterocytes
Female
Gene Expression
Histocompatibility Antigens Class I
Humans
Intestinal Mucosa
Macrophages
Male
Plasma Cells
Severity of Illness Index
Stress, Physiological
T-Lymphocytes
Broad MICA/B Expression in the Small Bowel Mucosa: A Link between Cellular Stress and Celiac Disease
topic_facet CD20 antigen
CD3 antigen
CD68 antigen
CD7 antigen
glycoprotein p 15095
major histocompatibility antigen class 1
major histocompatibility antigen class 2
syndecan 1
article
B lymphocyte
celiac disease
cell stress
cellular distribution
child
clinical article
confocal microscopy
controlled study
disease severity
endoplasmic reticulum stress
flow cytometry
gene
gene expression regulation
human
human cell
human tissue
immune dysregulation
immunofluorescence test
immunopathogenesis
intestine biopsy
lamina propria
macrophage
MICA gene
MICAB gene
oxidative stress
preschool child
protein localization
small intestine mucosa
B-Lymphocytes
Celiac Disease
Child, Preschool
Duodenum
Enterocytes
Female
Gene Expression
Histocompatibility Antigens Class I
Humans
Intestinal Mucosa
Macrophages
Male
Plasma Cells
Severity of Illness Index
Stress, Physiological
T-Lymphocytes
description The MICA/B genes (MHC class I chain related genes A and B) encode for non conventional class I HLA molecules which have no role in antigen presentation. MICA/B are up-regulated by different stress conditions such as heat-shock, oxidative stress, neoplasic transformation and viral infection. Particularly, MICA/B are expressed in enterocytes where they can mediate enterocyte apoptosis when recognised by the activating NKG2D receptor present on intraepithelial lymphocytes. This mechanism was suggested to play a major pathogenic role in active celiac disease (CD). Due to the importance of MICA/B in CD pathogenesis we studied their expression in duodenal tissue from CD patients. By immunofluorescence confocal microscopy and flow cytometry we established that MICA/B was mainly intracellularly located in enterocytes. In addition, we identified MICA/B+ T cells in both the intraepithelial and lamina propria compartments. We also found MICA/B+ B cells, plasma cells and some macrophages in the lamina propria. The pattern of MICA/B staining in mucosal tissue in severe enteropathy was similar to that found in in vitro models of cellular stress. In such models, MICA/B were located in stress granules that are associated to the oxidative and ER stress response observed in active CD enteropathy. Our results suggest that expression of MICA/B in the intestinal mucosa of CD patients is linked to disregulation of mucosa homeostasis in which the stress response plays an active role. © 2013 Allegretti et al.
title Broad MICA/B Expression in the Small Bowel Mucosa: A Link between Cellular Stress and Celiac Disease
title_short Broad MICA/B Expression in the Small Bowel Mucosa: A Link between Cellular Stress and Celiac Disease
title_full Broad MICA/B Expression in the Small Bowel Mucosa: A Link between Cellular Stress and Celiac Disease
title_fullStr Broad MICA/B Expression in the Small Bowel Mucosa: A Link between Cellular Stress and Celiac Disease
title_full_unstemmed Broad MICA/B Expression in the Small Bowel Mucosa: A Link between Cellular Stress and Celiac Disease
title_sort broad mica/b expression in the small bowel mucosa: a link between cellular stress and celiac disease
publishDate 2013
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_19326203_v8_n9_p_Allegretti
http://hdl.handle.net/20.500.12110/paper_19326203_v8_n9_p_Allegretti
_version_ 1768543488785252352