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Jonak C, Klosner G, Trautinger F. Heat shock proteins in the skin. Int J Cosmet Sci. 2006;28(4):233-41doi: 10.1111/j.1467-2494.2006.00327.x.
Jonak, C., Klosner, G., & Trautinger, F. (2006). Heat shock proteins in the skin. International journal of cosmetic science, 28(4), 233-41. https://doi.org/10.1111/j.1467-2494.2006.00327.x
Jonak, C, et al. "Heat shock proteins in the skin." International journal of cosmetic science vol. 28,4 (2006): 233-41. doi: https://doi.org/10.1111/j.1467-2494.2006.00327.x
Jonak C, Klosner G, Trautinger F. Heat shock proteins in the skin. Int J Cosmet Sci. 2006 Aug;28(4):233-41. doi: 10.1111/j.1467-2494.2006.00327.x. PMID: 18489262.
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Int J Cosmet Sci. 2006 Aug;28(4):233-41. doi: 10.1111/j.1467-2494.2006.00327.x.

Heat shock proteins in the skin.

International journal of cosmetic science

C Jonak, G Klosner, F Trautinger

Affiliations

  1. Department of Dermatology, Medical University of Vienna, Vienna, Austria.

PMID: 18489262 DOI: 10.1111/j.1467-2494.2006.00327.x

Abstract

Heat shock proteins (hsp) are expressed in all cells and organisms. Their expression is induced by heat shock (temperatures above 42 degrees C) and other forms of pathophysiological stress. Elevated levels of hsp protect cells from further stress exposure. Hsp are expressed intracellularly. They are highly conserved throughout evolution indicating hsp being necessary for survival under potentially harmful environmental conditions. Hsp are divided into families according to their molecular weight. The majority of hsp function as molecular chaperones. Chaperone function is characterized by binding to other proteins and mediating their folding, transport and interaction with other molecules. In human epidermis hsp are abundantly expressed and have been linked with functions in cell differentiation and photobiology. Recent research has mainly focused on the 27 and 72 kD hsp that are constitutively expressed in human keratinocytes. ultraviolet radiation (UV)-induced cell death and sunburn cell formation can be inhibited by previous heat shock exposure and UV itself can induce hsp expression. The expression of the 27 kD hsp (hsp27) in epidermal keratinocytes in situ and in culture correlates with differentiation. Expression of hsp27 increases simultaneously with keratinocyte differentiation. For that reason, hsp27 is described as a marker of epidermal differentiation. Changes in the expression and inducibility of hsp have been linked with ageing. In the skin, recent data indicate that hsp72 expression remains remarkably stable with intrinsic ageing. In contrast, levels of hsp27 have been found to be elevated in sun-protected aged skin indicating a link between hsp27 expression and age-dependent epidermal alterations. Regulation of hsp can be modified by pharmacological intervention and the development of safe topical and systemic treatments for the prevention of skin damage and disorders of keratinocyte differentiation can be expected for the future.

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