The isolation of human epidermal stem cells is critical for their clinical applications. In the present study, we isolated three populations of epidermal keratinocytes according to their ability to adhere to collagen type IV: i.e., rapidly adhering (RA), slowly adhering (SA), and non-adhering (NA) cells. The aim of this study was to characterize RA cells and to investigate the possibility of using these cells for epidermis reconstruction. To identify RA cells, flow cytometric analysis was performed using anti-alpha(6) integrin and anti-CD71 antibodies. RA cells express high levels of alpha(6) integrin and low levels of CD71, which are considered as markers of an epidermal stem cell nature. Furthermore, electron microscopy showed that RA cells are small and have a high nuclear to cytoplasmic ratio, whereas SA and NA cells have well-developed cellular organelles and abundant tonofilaments. Western blot analysis showed that RA cells are slow cycling and express p63, a putative epidermal stem cell marker, whereas SA and NA cells express c-Myc, which is known to regulate stem cell fate. To compare epidermal regenerative abilities, skin equivalents (SEs) were made using RA, SA, and NA cells. The epidermis constructed from RA cells was well formed compared to those formed from SA or NA cells. In addition, only SEs with RA cells expressed alpha(6) integrin and beta(1) integrin at the basal layer. These results indicate that RA cells represent epidermal stem cells and are predominately comprised of stem cells. Therefore, the isolation of RA cells using a simple technique offers a potential route to their clinical application, because they are easily isolated and provide a high yield of epidermal stem cells.

Abstract-Fingerprinting is an approach that assigns a unique and invisible ID to each sold instance of the intellectual property (IP). One of the key advantages fingerprinting-based intellectual property protection (IPP) has over watermarking-based IPP is the enabling of tracing stolen hardware or software. Fingerprinting schemes have been widely and effectively used to achieve this goal; however, their application domain has been restricted only to static artifacts, such as image and audio, where distinct copies can be obtained easily. In this paper, we propose the first generic fingerprinting technique that can be applied to an arbitrary synthesis (optimization or decision) or compilation problem and, therefore to hardware and software IPs.The key problem with design IP fingerprinting is that there is a need to generate a large number of structurally unique but functionally and timing identical designs. To reduce the cost of generating such distinct copies, we apply iterative optimization in an incremental fashion to solve a fingerprinted instance. Therefore, we leverage on the optimization effort already spent in obtaining previous solutions, yet we generate a uniquely fingerprinted new solution. This generic approach is the basis for developing specific fingerprinting techniques for four important problems in VLSI CAD: partitioning, graph coloring, satisfiability, and standard-cell placement. We demonstrate the effectiveness of the new fingerprintingbased IPP techniques on a number of standard benchmarks.

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Glycyl-L-histidyl-L-lysyl (GHK) possesses a high affinity for copper(II) ions, with which it spontaneously forms a complex (copper-GHK). It is well known that copper-GHK plays a physiological role in the process of wound healing and tissue repair by stimulating collagen synthesis in fibroblasts. This study was conducted to investigate the effects of copper-GHK on keratinocytes. Proliferative effects were analyzed and hematoxylin and eosin staining and immunohistochemistry were conducted to evaluate the effects of copper-GHK in skin equivalent (SE) models. In addition, western blotting was performed. In monolayer cultured keratinocytes, copper-GHK increased the proliferation of keratinocytes. When the SE models were evaluated, basal cells became cuboidal when copper-GHK was added. Immunohistochemical analysis revealed that copper-GHK increased proliferating cell nuclear antigen (PCNA) and p63 positivity. Furthermore, the expression of integrin alpha6 and beta1 increased in SE models, and these results were confirmed by Western blotting. The results of this study indicate that treatment with copper-GHK may increase the proliferative potential of basal keratinocytes by modulating the expression of integrins, p63 and PCNA. In addition, increased levels of p63, a putative stem cell marker of the skin, suggests that copper-GHK promotes the survival of basal stem cells in the skin.