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Repeated folding stress‐induced morphological changes in the dermal equivalent
Author(s) -
Arai Koji Y.,
Sugimoto Mami,
Ito Kanako,
Ogura Yuki,
Akutsu Nobuko,
Amano Satoshi,
Adachi Eijiro,
Nishiyama Toshio
Publication year - 2014
Publication title -
skin research and technology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.521
H-Index - 69
eISSN - 1600-0846
pISSN - 0909-752X
DOI - 10.1111/srt.12131
Subject(s) - skin equivalent , extracellular matrix , contraction (grammar) , hydroxyproline , biophysics , stress (linguistics) , chemistry , extracellular , biochemistry , biology , endocrinology , keratinocyte , linguistics , philosophy , in vitro
Background/purpose Repeated mechanical stresses applied to the same region of the skin are thought to induce morphological changes known as wrinkle. However, the underlying mechanisms are not fully understood. To study the mechanisms, we examined effects of repeated mechanical stress on the dermal equivalent. Methods We developed a novel device to apply repeated folding stress to the dermal equivalent. After applying the mechanical stress, morphological changes of the dermal equivalent and expression of several genes related to extracellular matrix turn over and cell contraction were examined. Results The repeated folding stress induced a noticeable decrease in the width of the dermal equivalent. The mechanical stress altered orientations of collagen fibrils. Hydroxyproline contents, dry weights and cell viability of the dermal equivalents were not affected by the mechanical stress. On the other hand, Rho‐associated coiled‐coil‐containing kinase ( ROCK ) specific inhibitor Y27632 completely suppressed the decrease in the width of the dermal equivalent. Conclusion The present results revealed that either degradation of collagen or changes in the number of cells were not responsible for the decrease in the width of the dermal equivalent and indicate that the repeated mechanical stress induces unidirectional contraction in the dermal equivalent through the RhoA‐ ROCK signaling pathway.

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