The effect of gamma keratose on cell viability in vitro after thermal stress and the regulation of cell death pathway-specific gene expression

被引:11
|
作者
Poranki, Deepika R. [1 ]
Van Dyke, Mark E. [2 ]
机构
[1] Wake Forest Sch Med, Wake Forest Inst Regenerat Med, Winston Salem, NC 27157 USA
[2] Virginia Polytech Inst & State Univ, Virginia Tech, Wake Forest Sch Biomed Engn & Sci, Blacksburg, VA 24061 USA
关键词
Keratin; Thermal; Apoptosis; Autophagy; Burn; Skin; TUMOR-NECROSIS-FACTOR; PROTEIN-KINASE-B; HEAT-SHOCK; INDUCED APOPTOSIS; L929; CELLS; AUTOPHAGY; AKT; ACTIVATION; SURVIVAL; TRANSDUCTION;
D O I
10.1016/j.biomaterials.2014.02.044
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
When skin is thermally burned, transfer of heat energy into the skin results in the destruction of cells. Some of these cells are damaged but may be capable of self-repair and survival, thereby contributing to spontaneous healing of the wound. Keratin protein-based biomaterials have been suggested as potential treatments for burn injury. Isolation of cortical proteins from hair fibers results in an acid soluble fraction of keratin proteins referred to as "gamma" keratose. In the present study, treatment with this fraction dissolved in media was able to maintain cell viability after thermal stress in an in vitro model using primary mouse dermal fibroblasts. PCR array analysis demonstrated that gamma keratose treatment may assist in the survival and salvage of thermally stressed cells by maintaining their viability through regulation of cell death pathway-related genes. Gamma keratose may be a promising biomaterial for burn treatment that aids in spontaneous wound healing from viable tissue surrounding the burn. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4646 / 4655
页数:10
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