Skip to content
2000
Volume 2, Issue 3
  • ISSN: 1573-3955
  • E-ISSN: 1875-631X

Abstract

Heat shock proteins exert their beneficial effects via basically two modes of action depending on their relative location within the host. Intracellular heat shock proteins found within cells serve a cytoprotective role by chaperoning naïve, misfolded and/or denatured proteins in response to stressful stimuli by a process known as the stress response. However, stressful stimuli also induce the release of intracellular heat shock proteins into the extracellular milieu and circulation. The extracellular heat shock protein serve a cytostimulatory role by initiating immune responses designed to fend off microbial infection and destroy neoplastic transformed cells. This review will briefly cover recent advances into elucidating the mechanism(s) by which stress induces the release of heat shock proteins into the circulation, how it initiates immune responses and suggest the possible biological significance of circulating Hsp to the host.

Loading

Article metrics loading...

/content/journals/cir/10.2174/157339506778018514
2006-08-01
2025-09-02
Loading full text...

Full text loading...

/content/journals/cir/10.2174/157339506778018514
Loading

  • Article Type:
    Research Article
Keyword(s): Cancer; chaperokine; heat shock proteins; inflammation; receptors; signal transduction
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test