The role of sialic acid-binding immunoglobulin-like-lectin-1 (siglec-1) in immunology and infectious disease.


Journal

International reviews of immunology
ISSN: 1563-5244
Titre abrégé: Int Rev Immunol
Pays: England
ID NLM: 8712260

Informations de publication

Date de publication:
2023
Historique:
pubmed: 9 9 2021
medline: 22 2 2023
entrez: 8 9 2021
Statut: ppublish

Résumé

Siglec-1, also known as Sialoadhesin (Sn) and CD169 is highly conserved among vertebrates and with 17 immunoglobulin-like domains is Siglec-1 the largest member of the Siglec family. Expression of Siglec-1 is found primarily on dendritic cells (DCs), macrophages and interferon induced monocyte. The structure of Siglec-1 is unique among siglecs and its function as a receptor is also different compared to other receptors in this class as it contains the most extracellular domains out of all the siglecs. However, the ability of Siglec-1 to internalize antigens and to pass them on to lymphocytes by allowing dendritic cells and macrophages to act as antigen presenting cells, is the main reason that has granted Siglec-1's key role in multiple human disease states including atherosclerosis, coronary artery disease, autoimmune diseases, cell-cell signaling, immunology, and more importantly bacterial and viral infections. Enveloped viruses for example have been shown to manipulate Siglec-1 to increase their virulence by binding to sialic acids present on the virus glycoproteins allowing them to spread or evade immune response. Siglec-1 mediates dissemination of HIV-1 in activated tissues enhancing viral spread via infection of DC/T-cell synapses. Overall, the ability of Siglec-1 to bind a variety of target cells within the immune system such as erythrocytes, B-cells, CD8+ granulocytes and NK cells, highlights that Siglec-1 is a unique player in these essential processes.

Identifiants

pubmed: 34494938
doi: 10.1080/08830185.2021.1931171
doi:

Substances chimiques

Sialic Acid Binding Ig-like Lectin 1 0
Sialic Acid Binding Immunoglobulin-like Lectins 0
Sialic Acids 0
Immunoglobulins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

113-138

Auteurs

Shane Prenzler (S)

School of Pharmacy and Medical Sciences, Griffith University, Gold Coast, Queensland, Australia.
Menzies Health Institute Queensland, Griffith University, Gold Coast, Queensland, Australia.

Santosh Rudrawar (S)

School of Pharmacy and Medical Sciences, Griffith University, Gold Coast, Queensland, Australia.
Menzies Health Institute Queensland, Griffith University, Gold Coast, Queensland, Australia.

Mario Waespy (M)

Centre for Biomolecular Interactions Bremen, Department of Biology and Chemistry, University of Bremen, Bremen, Germany.

Sørge Kelm (S)

Centre for Biomolecular Interactions Bremen, Department of Biology and Chemistry, University of Bremen, Bremen, Germany.

Shailendra Anoopkumar-Dukie (S)

School of Pharmacy and Medical Sciences, Griffith University, Gold Coast, Queensland, Australia.
Menzies Health Institute Queensland, Griffith University, Gold Coast, Queensland, Australia.

Thomas Haselhorst (T)

Institute for Glycomics, Griffith University, Gold Coast, Queensland, Australia.

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Classifications MeSH