Repeated folding stress-induced morphological changes in the dermal equivalent

被引:2
作者
Arai, Koji Y. [1 ]
Sugimoto, Mami [1 ]
Ito, Kanako [1 ]
Ogura, Yuki [2 ]
Akutsu, Nobuko [2 ]
Amano, Satoshi [2 ]
Adachi, Eijiro [3 ]
Nishiyama, Toshio [1 ]
机构
[1] Tokyo Univ Agr & Technol, Fac Agr, Scleroprot Res Inst, Fuchu, Tokyo 1838509, Japan
[2] Shiseido Res Ctr, Yokohama, Kanagawa, Japan
[3] Kitasato Univ, Grad Sch Med Sci, Dept Matrix Biol & Regenerat Med, Minato, Kanagawa, Japan
关键词
dermal equivalent; fibroblast; mechanical stress; skin furrow; wrinkle; COLLAGEN-MATRIX CONTRACTION; ENDOGENOUS CONTROL GENES; TIME QUANTITATIVE PCR; SMOOTH-MUSCLE-CELLS; GROWTH-FACTOR; FOCAL ADHESIONS; MECHANICAL SIGNALS; BASEMENT-MEMBRANE; TENASCIN-C; RHO-KINASE;
D O I
10.1111/srt.12131
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background/purposeRepeated 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. MethodsWe 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. ResultsThe 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. ConclusionThe 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.
引用
收藏
页码:399 / 408
页数:10
相关论文
共 37 条
[1]   Different molecular motors mediate platelet-derived growth factor and lysophosphatidic acid-stimulated floating collagen matrix contraction [J].
Abe, M ;
Ho, CH ;
Kamm, KE ;
Grinnell, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (48) :47707-47712
[2]   Formation of actin stress fibers and focal adhesions enhanced by Rho-kinase [J].
Amano, M ;
Chihara, K ;
Kimura, K ;
Fukata, Y ;
Nakamura, N ;
Matsuura, Y ;
Kaibuchi, K .
SCIENCE, 1997, 275 (5304) :1308-1311
[3]   Importance of balance between extracellular matrix synthesis and degradation in basement membrane formation [J].
Amano, S ;
Akutsu, N ;
Matsunaga, Y ;
Kadoya, K ;
Nishiyama, T ;
Champliaud, MF ;
Burgeson, RE ;
Adachi, E .
EXPERIMENTAL CELL RESEARCH, 2001, 271 (02) :249-262
[4]   Effects of vitamin C deficiency on the skin of the senescence marker protein-30 (SMP30) knockout mouse [J].
Arai, Koji Y. ;
Sato, Yasunori ;
Kondo, Yoshitaka ;
Kudo, Chikako ;
Tsuchiya, Hiroyuki ;
Nomura, Yoshihiro ;
Ishigami, Akihito ;
Nishiyama, Toshio .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2009, 385 (03) :478-483
[5]   Cell-matrix adhesion [J].
Berrier, Allison L. ;
Yamada, Kenneth M. .
JOURNAL OF CELLULAR PHYSIOLOGY, 2007, 213 (03) :565-573
[6]   Rho and Rac take center stage [J].
Burridge, K ;
Wennerberg, K .
CELL, 2004, 116 (02) :167-179
[7]  
Carmeliet G, 2001, CRIT REV EUKAR GENE, V11, P131
[8]   Regulation of extracellular matrix gene expression by mechanical stress [J].
Chiquet, M .
MATRIX BIOLOGY, 1999, 18 (05) :417-426
[9]   How do fibroblasts translate mechanical signals into changes in extracellular matrix production? [J].
Chiquet, M ;
Reneda, AS ;
Huber, F ;
Flück, M .
MATRIX BIOLOGY, 2003, 22 (01) :73-80
[10]   TENASCIN-C EXPRESSION BY FIBROBLASTS IS ELEVATED IN STRESSED COLLAGEN GELS [J].
CHIQUETEHRISMANN, R ;
TANNHEIMER, M ;
KOCH, M ;
BRUNNER, A ;
SPRING, J ;
MARTIN, D ;
BAUMGARTNER, S ;
CHIQUET, M .
JOURNAL OF CELL BIOLOGY, 1994, 127 (06) :2093-2101