Litcius/Paper detail

Chaperone duality: the role of extracellular and intracellular HSP70 as a biomarker of endothelial dysfunction in the development of atherosclerosis

Lílian Corrêa Costa‐Beber, Gabriela Elisa Hirsch, Thiago Gomes Heck, Mirna Stela Ludwig

2020Archives of Physiology and Biochemistry41 citationsDOI

Abstract

The 70-kDa heat shock proteins (HSP70) may provide relevant information about the endothelial dysfunction in cardiovascular diseases. Located in the intracellular milieu (iHSP70), they are essential chaperones that inhibit nuclear factor kappa B activation, stimulate nitric oxide production and superoxide dismutase activity, and inhibit apoptosis. However, under stressful conditions, HSP70 can be released into the extracellular medium (eHSP70) and act as an inflammatory mediator. Although studies have reported the vasoprotective role of iHSP70, the evidence regarding eHSP70 is contradictory. eHSP70 can activate NFκB and activator protein-1, thus stimulating the release of inflammatory cytokines and production of reactive oxygen species. Due to the antagonistic nature of HSP70 according to its location, the eHSP70/iHSP70 ratio (Heck index) has been proposed as a better marker of inflammatory status; however, more studies are required to confirm this hypothesis. Therefore, this review summarises studies that, together, describe the role of HSP70 in endothelial dysfunction.

Topics & Concepts

Endothelial dysfunctionIntracellularHsp70Activator (genetics)Cell biologyChaperone (clinical)ExtracellularHeat shock proteinNitric oxideReactive oxygen speciesSuperoxide dismutaseHSP60InflammationVasoprotectiveBiologyChemistryImmunologyBiochemistryMedicineEndocrinologyOxidative stressReceptorPathologyGeneHeat shock proteins researchThermoregulation and physiological responsesParaoxonase enzyme and polymorphisms