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Review
. 2011 May;16(3):235-49.
doi: 10.1007/s12192-010-0236-4. Epub 2010 Oct 21.

Extracellular heat shock proteins, cellular export vesicles, and the Stress Observation System: a form of communication during injury, infection, and cell damage. It is never known how far a controversial finding will go! Dedicated to Ferruccio Ritossa

Affiliations
Review

Extracellular heat shock proteins, cellular export vesicles, and the Stress Observation System: a form of communication during injury, infection, and cell damage. It is never known how far a controversial finding will go! Dedicated to Ferruccio Ritossa

Antonio De Maio. Cell Stress Chaperones. 2011 May.

Abstract

Heat shock proteins (hsp) have been found to play a fundamental role in the recovery from multiple stress conditions and to offer protection from subsequent insults. The function of hsp during stress goes beyond their intracellular localization and chaperone role as they have been detected outside cells activating signaling pathways. Extracellular hsp are likely to act as indicators of the stress conditions, priming other cells, particularly of the immune system, to avoid the propagation of the insult. Some extracellular hsp, for instance Hsp70, are associated with export vesicles, displaying a robust activation of macrophages. We have coined the term Stress Observation System (SOS) for the mechanism for sensing extracellular hsp, which we propose is a form of cellular communication during stress conditions. An enigmatic and still poorly understood process is the mechanism for the release of hsp, which do not contain any consensus secretory signal. The export of hsp appears to be a very complex phenomenon encompassing different alternative pathways. Moreover, extracellular hsp may not come in a single flavor, but rather in a variety of physical conditions. This review addresses some of our current knowledge about the release and function of extracellular hsp, in particular those associated with vesicles.

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Figures

Fig. 1
Fig. 1
Liposome aggregation induced by Hsp70, effect of cholesterol and GM1. The aggregation assay was performed with PS liposomes prepared with or without GM1 (20 μg/ml), cholesterol (20% mol/mol) or a combination of both. Liposomes were incubated with Hsp70 (10 μg/ml) in 40 mM histidine–HCl, pH 6, 300 mM sucrose, 0.5 mM MgCl2, 1 mM CaCl2 at 25°C, and the change in absorbance produced as a result of the aggregation process was measured at 350 nm in a Hewlett Packard spectrophotometer, with data collected every 30 s
Fig. 2
Fig. 2
Possible mechanisms for the interaction of extracellular vesicles containing Hsp70 and macrophages

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