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Skin-on-a-chip model simulating inflammation, edema and drug-based treatment.
Wufuer, Maierdanjiang; Lee, GeonHui; Hur, Woojune; Jeon, Byoungjun; Kim, Byung Jun; Choi, Tae Hyun; Lee, SangHoon.
Afiliação
  • Wufuer M; Department of Plastic and Reconstructive Surgery, Institute of Human-Environment Interface Biology, College of Medicine, Seoul Nat'l University, Seoul, Republic of Korea.
  • Lee G; Biomedical Research Institute, Seoul Nat'l Univ. Hospital, Seoul, Republic of Korea.
  • Hur W; KU-KIST Graduate School of Converging Science and Technology, Korea University, Republic of Korea.
  • Jeon B; Department of Plastic and Reconstructive Surgery, Institute of Human-Environment Interface Biology, College of Medicine, Seoul Nat'l University, Seoul, Republic of Korea.
  • Kim BJ; Biomedical Research Institute, Seoul Nat'l Univ. Hospital, Seoul, Republic of Korea.
  • Choi TH; Department of Plastic and Reconstructive Surgery, Institute of Human-Environment Interface Biology, College of Medicine, Seoul Nat'l University, Seoul, Republic of Korea.
  • Lee S; Biomedical Research Institute, Seoul Nat'l Univ. Hospital, Seoul, Republic of Korea.
Sci Rep ; 6: 37471, 2016 11 21.
Article em En | MEDLINE | ID: mdl-27869150
Recent advances in microfluidic cell cultures enable the construction of in vitro human skin models that can be used for drug toxicity testing, disease study. However, current in vitro skin model have limitations to emulate real human skin due to the simplicity of model. In this paper, we describe the development of 'skin-on-a-chip' to mimic the structures and functional responses of the human skin. The proposed model consists of 3 layers, on which epidermal, dermal and endothelial components originated from human, were cultured. The microfluidic device was designed for co-culture of human skin cells and each layer was separated by using porous membranes to allow interlayer communication. Skin inflammation and edema were induced by applying tumor necrosis factor alpha on dermal layer to demonstrate the functionality of the system. The expression levels of proinflammatory cytokines were analyzed to illustrate the feasibility. In addition, we evaluated the efficacy of therapeutic drug testing model using our skin chip. The function of skin barrier was evaluated by staining tight junctions and measuring a permeability of endothelium. Our results suggest that the skin-on-a-chip model can potentially be used for constructing in vitro skin disease models or for testing the toxicity of cosmetics or drugs.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pele / Edema / Dispositivos Lab-On-A-Chip / Inflamação / Modelos Biológicos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pele / Edema / Dispositivos Lab-On-A-Chip / Inflamação / Modelos Biológicos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article