W. Bowers et al., Artificial human skin: cytokine, prostaglandin, Hsp70 and histological responses to heat exposure, J DERMA SCI, 20(3), 1999, pp. 172-182
Artificial human skin, Skin(2)(TM) (keratinocytes and fibroblasts) and EpiD
erm(TM) (keratinocytes), was used to determine heat-induced release/accumul
ation of mediators of injury and repair. Skin(2) was exposed to 37 or 41-45
degrees C for 90 min, followed by 37 degrees C for 22.5 h. Media were anal
yzed for interleukin-1 alpha (IL-1 alpha), prostaglandin-E, (PGE), thrombox
ane-B-2 (TxB(2)) and nuclear matrix apparatus protein (NMAP, viability). Sp
ecimens were taken for microscopy. Media and lysates from Skin(2) and EpiDe
rm (37 and 45 degrees C) were analyzed for IL-1 alpha, its soluble receptor
(sIL-1RII), receptor antagonist (IL-1Ra), interleukin-6 (IL-6) and heat sh
ock protein-70A (lysates only). Significant release of IL-1 alpha and PGE,
was detected only above 43 degrees C, where viability deteriorated and hist
ological damage (especially to keratinocytes) was observed. With both skin
products, sIL-1RII release was heat-depressed. IL-1 alpha and IL-1Ra were e
levated in media and IL-1Ra appeared to lower the bioactivity of IL-1 alpha
. Heat depressed IL-6 release from Skin(2) fibroblasts. IL-6 production and
release were negligible with EpiDerm. Heat increased Hsp-70A in both produ
cts. We conclude keratinocytes and fibroblasts are not primary cytokine and
prostaglandin sources in heatstroke ( < 44 degrees C) but could be in evap
orative cooling failure, focal hot spots, or systemic responses. Levels of
IL-1Ra. PGE(2) and Hsp70A may be important markers of cell status. (C) 1999
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