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Siglecs in Brain Function and Neurological Disorders

Siglecs (Sialic acid-binding immunoglobulin-type lectins) are a I-type lectin that typically binds sialic acid. Siglecs are predominantly expressed in immune cells and generate activating or inhibitory signals. They are also shown to be expressed on the surface of cells in the nervous system and hav...

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Autores principales: Siddiqui, Shoib Sarwar, Matar, Rachel, Merheb, Maxime, Hodeify, Rawad, Vazhappilly, Cijo George, Marton, John, Shamsuddin, Syed Azharuddin, Al Zouabi, Hussain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829431/
https://www.ncbi.nlm.nih.gov/pubmed/31546700
http://dx.doi.org/10.3390/cells8101125
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author Siddiqui, Shoib Sarwar
Matar, Rachel
Merheb, Maxime
Hodeify, Rawad
Vazhappilly, Cijo George
Marton, John
Shamsuddin, Syed Azharuddin
Al Zouabi, Hussain
author_facet Siddiqui, Shoib Sarwar
Matar, Rachel
Merheb, Maxime
Hodeify, Rawad
Vazhappilly, Cijo George
Marton, John
Shamsuddin, Syed Azharuddin
Al Zouabi, Hussain
author_sort Siddiqui, Shoib Sarwar
collection PubMed
description Siglecs (Sialic acid-binding immunoglobulin-type lectins) are a I-type lectin that typically binds sialic acid. Siglecs are predominantly expressed in immune cells and generate activating or inhibitory signals. They are also shown to be expressed on the surface of cells in the nervous system and have been shown to play central roles in neuroinflammation. There has been a plethora of reviews outlining the studies pertaining to Siglecs in immune cells. However, this review aims to compile the articles on the role of Siglecs in brain function and neurological disorders. In humans, the most abundant Siglecs are CD33 (Siglec-3), Siglec-4 (myelin-associated glycoprotein/MAG), and Siglec-11, Whereas in mice the most abundant are Siglec-1 (sialoadhesin), Siglec-2 (CD22), Siglec-E, Siglec-F, and Siglec-H. This review is divided into three parts. Firstly, we discuss the general biological aspects of Siglecs that are expressed in nervous tissue. Secondly, we discuss about the role of Siglecs in brain function and molecular mechanism for their function. Finally, we collate the available information on Siglecs and neurological disorders. It is intriguing to study this family of proteins in neurological disorders because they carry immunoinhibitory and immunoactivating motifs that can be vital in neuroinflammation.
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spelling pubmed-68294312019-11-18 Siglecs in Brain Function and Neurological Disorders Siddiqui, Shoib Sarwar Matar, Rachel Merheb, Maxime Hodeify, Rawad Vazhappilly, Cijo George Marton, John Shamsuddin, Syed Azharuddin Al Zouabi, Hussain Cells Review Siglecs (Sialic acid-binding immunoglobulin-type lectins) are a I-type lectin that typically binds sialic acid. Siglecs are predominantly expressed in immune cells and generate activating or inhibitory signals. They are also shown to be expressed on the surface of cells in the nervous system and have been shown to play central roles in neuroinflammation. There has been a plethora of reviews outlining the studies pertaining to Siglecs in immune cells. However, this review aims to compile the articles on the role of Siglecs in brain function and neurological disorders. In humans, the most abundant Siglecs are CD33 (Siglec-3), Siglec-4 (myelin-associated glycoprotein/MAG), and Siglec-11, Whereas in mice the most abundant are Siglec-1 (sialoadhesin), Siglec-2 (CD22), Siglec-E, Siglec-F, and Siglec-H. This review is divided into three parts. Firstly, we discuss the general biological aspects of Siglecs that are expressed in nervous tissue. Secondly, we discuss about the role of Siglecs in brain function and molecular mechanism for their function. Finally, we collate the available information on Siglecs and neurological disorders. It is intriguing to study this family of proteins in neurological disorders because they carry immunoinhibitory and immunoactivating motifs that can be vital in neuroinflammation. MDPI 2019-09-22 /pmc/articles/PMC6829431/ /pubmed/31546700 http://dx.doi.org/10.3390/cells8101125 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Siddiqui, Shoib Sarwar
Matar, Rachel
Merheb, Maxime
Hodeify, Rawad
Vazhappilly, Cijo George
Marton, John
Shamsuddin, Syed Azharuddin
Al Zouabi, Hussain
Siglecs in Brain Function and Neurological Disorders
title Siglecs in Brain Function and Neurological Disorders
title_full Siglecs in Brain Function and Neurological Disorders
title_fullStr Siglecs in Brain Function and Neurological Disorders
title_full_unstemmed Siglecs in Brain Function and Neurological Disorders
title_short Siglecs in Brain Function and Neurological Disorders
title_sort siglecs in brain function and neurological disorders
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829431/
https://www.ncbi.nlm.nih.gov/pubmed/31546700
http://dx.doi.org/10.3390/cells8101125
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