Multiplicity of Glycosphingolipid-Enriched Microdomain-Driven Immune Signaling

• Main Authors: Noriko Yokoyama, Kei Hanafusa, Tomomi Hotta, Eriko Oshima, Kazuhisa Iwabuchi, Hitoshi Nakayama
• Format: Article
• Language: English
• Published: MDPI AG 2021-09-01
• Series: International Journal of Molecular Sciences
• Subjects: glycosphingolipids; microdomain; immune signaling
• Online Access: https://www.mdpi.com/1422-0067/22/17/9565
• ISSN: 1661-6596; 1422-0067

Glycosphingolipids (GSLs), together with cholesterol, sphingomyelin (SM), and glycosylphosphatidylinositol (GPI)-anchored and membrane-associated signal transduction molecules, form GSL-enriched microdomains. These specialized microdomains interact in a <i>cis</i> manner with various immune receptors, affecting immune receptor-mediated signaling. This, in turn, results in the regulation of a broad range of immunological functions, including phagocytosis, cytokine production, antigen presentation and apoptosis. In addition, GSLs alone can regulate immunological functions by acting as ligands for immune receptors, and exogenous GSLs can alter the organization of microdomains and microdomain-associated signaling. Many pathogens, including viruses, bacteria and fungi, enter host cells by binding to GSL-enriched microdomains. Intracellular pathogens survive inside phagocytes by manipulating intracellular microdomain-driven signaling and/or sphingolipid metabolism pathways. This review describes the mechanisms by which GSL-enriched microdomains regulate immune signaling.