Dynamics of heat shock protein 70 kDa in heat-shocked and hypoxic human endothelial cells

Author(s)

Coimbra, Luiza B. C. T. ; Pinto-Martinez, Andrea ; Pavan, Isadora C. B. ; Melo, Everton G. ; Araujo, Thais L. S.

• Document type: Journal article
• Source: CELL STRESS & CHAPERONES; v. 30, n. 4, p. 16-pg., 2025-07-01.

Abstract

Heat shock proteins (HSPs) play crucial roles in human endothelial cell functions such as migration and angiogenesis. However, human HSP dynamics under stress conditions such as heat shock (HS) and hypoxia in human endothelial cells (ECs) are enigmatic, and the characteristics of HSPs in ECs after exposure to thermal stress and a low-oxygen environment are unknown. We hypothesized that ECs adapt to HS and hypoxia by modulating chaperome oligomerization and that HSP70 is a major determinant of the endothelial phenotype. HSP70 inhibition with VER-155008 or YM-1 in primary human endothelial cells decreases EC proliferation, migration, and angiogenesis at baseline and after heat shock recovery. We showed that vascular-independent HSC/P70 multimeric complexes in primary human veins (HUVEC) and coronary artery ECs (HCAEC) accumulate after HS and are decreased by hypoxia. HS recovery increases the number of HSP90 dimers, inducible HSP70, and HSP40 macromolecular complexes, whereas HSC70 returns to baseline. We demonstrated that the HS response and hypoxia regulate HSPs through a new layer of complexity, oligomerization, in addition to classical cochaperone/NEF interactions. The biphasic temporal oligomerization of molecular chaperones in the recovery phase provides a novel face of the heat shock response. In addition, shifts in the subcellular location and upregulation of HSP70 were also observed here. The decrease in HSP expression caused by hypoxia raises the possibility that decreased chaperone power contributes to the endothelial dysfunction found in atherosclerosis, thrombosis, and cancer. Together, these results show that HSP70 is pivotal to the healthy endothelial response in veins and coronary arteries, and we revealed human HSP dynamics in the vascular response to proteotoxic stress. (AU)

• FAPESP's process: 19/20435-8 - Molecular chaperone HSP70 mediates proteostasis in endothelial cells response to hemodynamic force
• Grantee: Thaís Larissa Araujo de Oliveira Silva
• Support Opportunities: Scholarships in Brazil - Young Researchers
• FAPESP's process: 20/11249-3 - The pathophysiology of endothelial cells isolated from patients with hypertensive pulmonary thromboembolism: mechanisms regulated by HSP70
• Grantee: Luiza Bitencourt de Carvalho Terci Coimbra
• Support Opportunities: Scholarships in Brazil - Master
• FAPESP's process: 18/13739-8 - Molecular chaperone HSP70 mediates proteostasis in endothelial cells response to hemodynamic force
• Grantee: Thaís Larissa Araujo de Oliveira Silva
• Support Opportunities: Research Grants - Young Investigators Grants
• FAPESP's process: 23/06938-2 - Standardization of BONCAT coupled to PLA in primary endothelial cells.
• Grantee: Isadora Carolina Betim Pavan
• Support Opportunities: Scholarships in Brazil - Technical Training Program - Technical Training
• FAPESP's process: 19/25503-1 - Mechanism of formation and stability of macromolecular complexes of Hsp70 and Hsp90 in endothelial cells
• Grantee: Everton Gonzaga de Melo
• Support Opportunities: Scholarships in Brazil - Scientific Initiation
• FAPESP's process: 24/20224-5 - Standardization of BONCAT coupled to PLA in primary endothelial cells.
• Grantee: Andrea Katherine Pinto Martinez
• Support Opportunities: Scholarships in Brazil - Technical Training Program - Technical Training