Regulatory Circuits Mediated by Lectin-Glycan Interactions in Autoimmunity and Cancer

Numerous regulatory programs have been identified that contribute to the restoration of homeostasis at the conclusion of immune responses and to safeguarding against the detrimental effects of chronic inflammation and autoimmune pathology. Malignant cells may usurp these pathways to create immunosup...

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Autor principal: Croci Russo, Diego Omar
Publicado: 2012
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_10747613_v36_n3_p322_Rabinovich
http://hdl.handle.net/20.500.12110/paper_10747613_v36_n3_p322_Rabinovich
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spelling paper:paper_10747613_v36_n3_p322_Rabinovich2023-06-08T16:05:10Z Regulatory Circuits Mediated by Lectin-Glycan Interactions in Autoimmunity and Cancer Croci Russo, Diego Omar carcinoembryonic antigen related cell adhesion molecule 1 CD22 antigen cytotoxic T lymphocyte antigen 4 dectin 1 galectin glycan glycosidase glycosyltransferase immunoglobulin interleukin 10 interleukin 12 interleukin 6 lectin mitogen activated protein kinase protein tyrosine kinase tumor necrosis factor receptor 1 antigen presenting cell autoimmune disease autoimmunity carbohydrate synthesis cell death cell migration cell survival cytokine production endocytosis enzyme activation glycosylation immune response immunocompetent cell immunological tolerance inflammation lymphocyte activation neoplasm priority journal protein interaction protein motif protein phosphorylation protein structure regulatory mechanism regulatory T lymphocyte review Animals Antigen-Presenting Cells Autoimmunity Cell Death Humans Immune Tolerance Inflammation Lectins Lymphocyte Activation Mice Models, Immunological Neoplasms Polysaccharides Signal Transduction T-Lymphocytes Numerous regulatory programs have been identified that contribute to the restoration of homeostasis at the conclusion of immune responses and to safeguarding against the detrimental effects of chronic inflammation and autoimmune pathology. Malignant cells may usurp these pathways to create immunosuppressive networks that thwart antitumor responses. Herein we review the role of endogenous lectins (C-type lectins, siglecs, and galectins) and specific N- and O-glycans generated by the coordinated action of glycosyltransferases and glycosidases that together promote regulatory signals that control immune cell homeostasis. We also discuss the mechanisms by which glycan-dependent regulatory programs integrate into canonical circuits that amplify or silence immune responses related to autoimmunity and neoplastic disease. © 2012 Elsevier Inc.. Fil:Croci, D.O. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2012 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_10747613_v36_n3_p322_Rabinovich http://hdl.handle.net/20.500.12110/paper_10747613_v36_n3_p322_Rabinovich
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic carcinoembryonic antigen related cell adhesion molecule 1
CD22 antigen
cytotoxic T lymphocyte antigen 4
dectin 1
galectin
glycan
glycosidase
glycosyltransferase
immunoglobulin
interleukin 10
interleukin 12
interleukin 6
lectin
mitogen activated protein kinase
protein tyrosine kinase
tumor necrosis factor receptor 1
antigen presenting cell
autoimmune disease
autoimmunity
carbohydrate synthesis
cell death
cell migration
cell survival
cytokine production
endocytosis
enzyme activation
glycosylation
immune response
immunocompetent cell
immunological tolerance
inflammation
lymphocyte activation
neoplasm
priority journal
protein interaction
protein motif
protein phosphorylation
protein structure
regulatory mechanism
regulatory T lymphocyte
review
Animals
Antigen-Presenting Cells
Autoimmunity
Cell Death
Humans
Immune Tolerance
Inflammation
Lectins
Lymphocyte Activation
Mice
Models, Immunological
Neoplasms
Polysaccharides
Signal Transduction
T-Lymphocytes
spellingShingle carcinoembryonic antigen related cell adhesion molecule 1
CD22 antigen
cytotoxic T lymphocyte antigen 4
dectin 1
galectin
glycan
glycosidase
glycosyltransferase
immunoglobulin
interleukin 10
interleukin 12
interleukin 6
lectin
mitogen activated protein kinase
protein tyrosine kinase
tumor necrosis factor receptor 1
antigen presenting cell
autoimmune disease
autoimmunity
carbohydrate synthesis
cell death
cell migration
cell survival
cytokine production
endocytosis
enzyme activation
glycosylation
immune response
immunocompetent cell
immunological tolerance
inflammation
lymphocyte activation
neoplasm
priority journal
protein interaction
protein motif
protein phosphorylation
protein structure
regulatory mechanism
regulatory T lymphocyte
review
Animals
Antigen-Presenting Cells
Autoimmunity
Cell Death
Humans
Immune Tolerance
Inflammation
Lectins
Lymphocyte Activation
Mice
Models, Immunological
Neoplasms
Polysaccharides
Signal Transduction
T-Lymphocytes
Croci Russo, Diego Omar
Regulatory Circuits Mediated by Lectin-Glycan Interactions in Autoimmunity and Cancer
topic_facet carcinoembryonic antigen related cell adhesion molecule 1
CD22 antigen
cytotoxic T lymphocyte antigen 4
dectin 1
galectin
glycan
glycosidase
glycosyltransferase
immunoglobulin
interleukin 10
interleukin 12
interleukin 6
lectin
mitogen activated protein kinase
protein tyrosine kinase
tumor necrosis factor receptor 1
antigen presenting cell
autoimmune disease
autoimmunity
carbohydrate synthesis
cell death
cell migration
cell survival
cytokine production
endocytosis
enzyme activation
glycosylation
immune response
immunocompetent cell
immunological tolerance
inflammation
lymphocyte activation
neoplasm
priority journal
protein interaction
protein motif
protein phosphorylation
protein structure
regulatory mechanism
regulatory T lymphocyte
review
Animals
Antigen-Presenting Cells
Autoimmunity
Cell Death
Humans
Immune Tolerance
Inflammation
Lectins
Lymphocyte Activation
Mice
Models, Immunological
Neoplasms
Polysaccharides
Signal Transduction
T-Lymphocytes
description Numerous regulatory programs have been identified that contribute to the restoration of homeostasis at the conclusion of immune responses and to safeguarding against the detrimental effects of chronic inflammation and autoimmune pathology. Malignant cells may usurp these pathways to create immunosuppressive networks that thwart antitumor responses. Herein we review the role of endogenous lectins (C-type lectins, siglecs, and galectins) and specific N- and O-glycans generated by the coordinated action of glycosyltransferases and glycosidases that together promote regulatory signals that control immune cell homeostasis. We also discuss the mechanisms by which glycan-dependent regulatory programs integrate into canonical circuits that amplify or silence immune responses related to autoimmunity and neoplastic disease. © 2012 Elsevier Inc..
author Croci Russo, Diego Omar
author_facet Croci Russo, Diego Omar
author_sort Croci Russo, Diego Omar
title Regulatory Circuits Mediated by Lectin-Glycan Interactions in Autoimmunity and Cancer
title_short Regulatory Circuits Mediated by Lectin-Glycan Interactions in Autoimmunity and Cancer
title_full Regulatory Circuits Mediated by Lectin-Glycan Interactions in Autoimmunity and Cancer
title_fullStr Regulatory Circuits Mediated by Lectin-Glycan Interactions in Autoimmunity and Cancer
title_full_unstemmed Regulatory Circuits Mediated by Lectin-Glycan Interactions in Autoimmunity and Cancer
title_sort regulatory circuits mediated by lectin-glycan interactions in autoimmunity and cancer
publishDate 2012
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_10747613_v36_n3_p322_Rabinovich
http://hdl.handle.net/20.500.12110/paper_10747613_v36_n3_p322_Rabinovich
work_keys_str_mv AT crocirussodiegoomar regulatorycircuitsmediatedbylectinglycaninteractionsinautoimmunityandcancer
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