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Mol. Cells 2008; 25(1): 99-104

Published online January 1, 1970

© The Korean Society for Molecular and Cellular Biology

Contribution of TLR2 to the Initiation of Ganglioside-triggered Inflammatory Signaling

Hee Jung Yoon, Sae Bom Jeon, Kyoungho Suk, Dong-Kug Choi, Young-Joon Hong and Eun Jung Park

Abstract

Gangliosides, sialic acid-containing glycosphingolipids, are implicated in many neuronal diseases, but the precise molecular mechanisms underlying their pathological activities are poorly understood. Here we report that TLR2 participates in the initiation of ganglioside-triggered inflammatory signaling responses. Using FACS analysis and immunofluorescence microscopy, we found that gangliosides rapidly enhanced the cell surface expression of TLR2 in microglia, while reducing that of TLR4. The ganglioside-dependent increase of TLR2 expression was also observed at the messenger and protein levels. We also showed that gangliosides stimulate the interaction of TLR2 with Myd88, an adaptor for TLRs, and obtained evidence that lipid raft formation is closely associated with the ganglioside-induced activation of TLR2 and subsequent inflammatory signaling. These results collectively suggest that TLR2 contributes to the ability of gangliosides to cause inflammatory conditions in the brain.

Keywords Adaptor; Astrocytes; Brain; Endogenous Ligand; Gangliosides; Inflammation; Microglia; Myd88; TLR2

Article

Research Article

Mol. Cells 2008; 25(1): 99-104

Published online February 29, 2008

Copyright © The Korean Society for Molecular and Cellular Biology.

Contribution of TLR2 to the Initiation of Ganglioside-triggered Inflammatory Signaling

Hee Jung Yoon, Sae Bom Jeon, Kyoungho Suk, Dong-Kug Choi, Young-Joon Hong and Eun Jung Park

Abstract

Gangliosides, sialic acid-containing glycosphingolipids, are implicated in many neuronal diseases, but the precise molecular mechanisms underlying their pathological activities are poorly understood. Here we report that TLR2 participates in the initiation of ganglioside-triggered inflammatory signaling responses. Using FACS analysis and immunofluorescence microscopy, we found that gangliosides rapidly enhanced the cell surface expression of TLR2 in microglia, while reducing that of TLR4. The ganglioside-dependent increase of TLR2 expression was also observed at the messenger and protein levels. We also showed that gangliosides stimulate the interaction of TLR2 with Myd88, an adaptor for TLRs, and obtained evidence that lipid raft formation is closely associated with the ganglioside-induced activation of TLR2 and subsequent inflammatory signaling. These results collectively suggest that TLR2 contributes to the ability of gangliosides to cause inflammatory conditions in the brain.

Keywords: Adaptor, Astrocytes, Brain, Endogenous Ligand, Gangliosides, Inflammation, Microglia, Myd88, TLR2

Mol. Cells
Nov 30, 2023 Vol.46 No.11, pp. 655~725
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Molecules and Cells

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