TY - JOUR
T1 - 24-hour rhythm of aquaporin-3 function in the epidermis is regulated by molecular clocks
AU - Matsunaga, Naoya
AU - Itcho, Kazufumi
AU - Hamamura, Kengo
AU - Ikeda, Eriko
AU - Ikeyama, Hisako
AU - Furuichi, Yoko
AU - Watanabe, Miyako
AU - Koyanagi, Satoru
AU - Ohdo, Shigehiro
N1 - Funding Information:
This study was supported in part by Grants-in-Aid for Scientific Research (A; 25253038; S. Ohdo), for Scientific Research on Innovative Areas (25136716; S. Ohdo), and for Challenging Exploratory Research (25670079; S. Ohdo) and Scientific Research (C; 24590196; N. Matsunaga) from the Japan Society for the Promotion of Science (JSPS) and the Fukuoka Foundation for Sound Health. This work was supported by Platform for Drug Discovery, Informatics, and Structural Life Science from the Ministry of Education, Culture, Sports, Science and Technology, Japan, and the Research Support Center, Graduate School of Medical Sciences, Kyushu University is acknowledged for their technical support.
Publisher Copyright:
© 2014 The Society for Investigative Dermatology.
PY - 2014
Y1 - 2014
N2 - Aquaporin 3 (AQP3) is located in the basal layer of the epidermis and regulates biological functions of skin such as water content and trans-epidermal water loss. A recent study showed that the biological function of skin exhibits a 24-hour rhythm, but the molecular mechanism of the variation remains poorly understood. Here we show that mice mutated in the core clock component CLOCK (Clk/Clk) show decreased stratum corneum hydration. An extensive search for the underlying cause led us to identify AQP3 as a new regulator to control the 24-hour variation in biological functions of skin. In mouse epidermis of wild-type mice, mAqp3 exhibits circadian rhythms; however, these are significantly decreased in Clk/Clk. Luciferase reporter gene analysis revealed that transcription of mAqp3 is activated by D-site-binding protein, a clock gene. A human homolog, hAQP3, also exhibited significant oscillation in human keratinocyte (HaCaT) cells synchronized with medium containing 50% serum, and this rhythm was regulated by the endogenous CLOCK/BMAL1 heterodimer. These data indicate that although the molecular mechanisms underlying the rhythmic expression of mAqp3 and hAQP3 are different, clock genes are involved in time-dependent skin hydration. Our current findings provide a molecular link between the circadian clock and AQP3 function in mouse dorsal skin and HaCaT cells.
AB - Aquaporin 3 (AQP3) is located in the basal layer of the epidermis and regulates biological functions of skin such as water content and trans-epidermal water loss. A recent study showed that the biological function of skin exhibits a 24-hour rhythm, but the molecular mechanism of the variation remains poorly understood. Here we show that mice mutated in the core clock component CLOCK (Clk/Clk) show decreased stratum corneum hydration. An extensive search for the underlying cause led us to identify AQP3 as a new regulator to control the 24-hour variation in biological functions of skin. In mouse epidermis of wild-type mice, mAqp3 exhibits circadian rhythms; however, these are significantly decreased in Clk/Clk. Luciferase reporter gene analysis revealed that transcription of mAqp3 is activated by D-site-binding protein, a clock gene. A human homolog, hAQP3, also exhibited significant oscillation in human keratinocyte (HaCaT) cells synchronized with medium containing 50% serum, and this rhythm was regulated by the endogenous CLOCK/BMAL1 heterodimer. These data indicate that although the molecular mechanisms underlying the rhythmic expression of mAqp3 and hAQP3 are different, clock genes are involved in time-dependent skin hydration. Our current findings provide a molecular link between the circadian clock and AQP3 function in mouse dorsal skin and HaCaT cells.
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U2 - 10.1038/jid.2014.13
DO - 10.1038/jid.2014.13
M3 - Article
C2 - 24418925
AN - SCOPUS:84900857843
SN - 0022-202X
VL - 134
SP - 1636
EP - 1644
JO - Journal of Investigative Dermatology
JF - Journal of Investigative Dermatology
IS - 6
ER -