Several mechanisms are involved in the protective responses to PDT including the expression of chaperone/heat shock proteins (HSPs).
First-pass extracted concept
heat shock proteins
Aliases
HSPs
Evidence Snippets
The necessity to focus on the role of anti-inflammatory mediators, as well as the pathogenetic significance of important molecular groups, such as the heat shock proteins, which until now have been given scant attention, will be stressed.
Supporting Sources
Linked Claims
Heat shock proteins can promote cell survival through cytoprotective mechanisms.
it has been discovered that HSPs can play an important role in cell survival, due to the fact that they are responsible for many cytoprotective mechanisms
Extracellular or membrane-bound heat shock proteins mediate immunological functions.
In contrast, extracellular HSPs or membrane-bound HSPs mediate immunological functions.
Heat shock protein expression is part of the protective cellular response to photodynamic therapy.
Several mechanisms are involved in the protective responses to PDT including the expression of chaperone/heat shock proteins (HSPs).
Intracellular heat shock proteins are associated with anti-apoptotic function, and HSP-induced autophagy is described as protective.
In general, intracellular HSPs have been related to an anti-apoptotic function and recently, HSP-induced autophagy has shown to have a protective role in these chaperones.
The review discusses how certain photodynamic therapy protocols may optimally stimulate the immune system through heat shock proteins.
We will also discuss how certain PDT protocols optimally stimulate the immune system through HSPs.
The review argues that anti-inflammatory mediators and heat shock proteins deserve greater attention in sepsis microcirculatory pathogenesis and therapy discussions.