Macrophage Galactose C-type Lectin Exacerbates MS Pathogenesis in EAE Murine Model (P6-1.001)

Multiple sclerosis (MS) is a chronic autoimmune disorder affecting the central nervous system (CNS), leading to neuroinflammation, gliosis, and neuronal loss. The human macrophage galactose-type lectin (MGL or CD301), a member of the C-type lectin receptor (CLR) family, is expressed by myeloid cells such as dendritic cells (DCs) and macrophages. In mice, the macrophage galactose-type lectin 2 (MGL2 or CD301b) receptor is homologous to the human MGL. This study investigates the role of MGL2 in the progression of experimental autoimmune encephalomyelitis (EAE), a murine model replicating MS disease.

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Publication Details

Journal
Neurology
Published
2025-04-07
DOI
https://doi.org/10.1212/wnl.0000000000211365
Primary Topic
Immune Cell Function and Interaction
Type
article
Field-Weighted Citation Impact
0.00
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article

Macrophage Galactose C-type Lectin Exacerbates MS Pathogenesis in EAE Murine Model (P6-1.001)

Fikri Y. Avci, Mariye Erol Demirturk
Neurology
Immune Cell Function and Interaction
article

Macrophage Galactose C-type Lectin Exacerbates MS Pathogenesis in EAE Murine Model (P6-1.001)

Fikri Y. Avci, Mariye Erol Demirturk
article en

Abstract

Multiple sclerosis (MS) is a chronic autoimmune disorder affecting the central nervous system (CNS), leading to neuroinflammation, gliosis, and neuronal loss. The human macrophage galactose-type lectin (MGL or CD301), a member of the C-type lectin receptor (CLR) family, is expressed by myeloid cells such as dendritic cells (DCs) and macrophages. In mice, the macrophage galactose-type lectin 2 (MGL2 or CD301b) receptor is homologous to the human MGL. This study investigates the role of MGL2 in the progression of experimental autoimmune encephalomyelitis (EAE), a murine model replicating MS disease.

NeurologyVol. 104(7_Supplement_1)
Emory University (US)
Zero hunger
Openalex Percentile: Top 92%
Immune Cell Function and Interaction
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