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Studies of Chaperone-Cochaperone Interactions using Homogenous Bead-Based Assay
Published on: July 21, 2021
Spatiotemporal Regulation of Hsp90-Ligand Complex Leads to Immune Activation
Yasuaki Tamura1, Akihiro Yoneda1, Norio Takei1
1Department of Molecular Therapeutics, Center for Food and Medical Innovation, Institute for Innovation and Business Promotion, Hokkaido University , Sapporo , Japan.
Abstract:
Although heat shock proteins (HSPs) primarily play a pivotal role in the maintenance of cellular homeostasis while reducing extracellular as well as intracellular stresses, their role in immunologically relevant scenarios, including activation of innate immunity as danger signals, antitumor immunity, and autoimmune diseases, is now gaining much attention. The most prominent feature of HSPs is that they function both in their own and as an HSP-ligand complex. We here show as a unique feature of extracellular HSPs that they target chaperoned molecules into a particular endosomal compartment of dendritic cells, thereby inducing innate and adaptive immune responses via spatiotemporal regulation.
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