Extracellular Hsp90 and protection of neuronal cells through Nrf2

Author:

Calderwood Stuart K.1ORCID,Borges Thiago J.2,Eguchi Takanori3,Lang Benjamin J.1,Murshid Ayesha14,Okusha Yuka1,Prince Thomas L.15

Affiliation:

1. Department of Radiation Oncology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, U.S.A.

2. Center for Transplantation Science, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02129, U.S.A.

3. Department of Dental Pharmacology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama 700-8525, Japan

4. Acrivon Therapeutics, 480 Arsenal Way, Watertown, MA 02472, U.S.A.

5. Ranok Therapeutics, Waltham, MA 02451, U.S.A.

Abstract

Heat shock protein 90 (Hsp90), although one of the most essential intracellular chaperones, can also play key roles in the extracellular milieu. Here, we review the properties of extracellular Hsp90 in cellular homeostasis in the heat shock response (HSR), focusing on cells of the central nervous system. Hsp90 can be secreted by microglia as well as other cell types by non-canonical pathways of secretion. The chaperone may then influence the behavior of distant cells and can for instance protect neuronal cells from the oxidative burst accompanying phagocytosis by microglia of beta-amyloid fibrils. A mechanism involving activation of the transcription factor Nrf2, and induction of the antioxidant response is reported. We review the potential role of extracellular Hsp90, Nrf2 and transcellular chaperone signaling in the non-cell-intrinsic HSR.

Publisher

Portland Press Ltd.

Subject

Biochemistry

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