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Angiopoietin-related growth factor (AGF) promotes epidermal proliferation, remodeling, and regeneration
Author(s) -
Yuichi Oike,
Kunio Yasunaga,
Yasuhiro Ito,
Shun-ichiro Matsumoto,
Hiromitsu Maekawa,
Tohru Morisada,
Fumio Arai,
Naomi Nakagata,
Motohiro Takeya,
Yasuhiko Masuho,
Toshio Suda
Publication year - 2003
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1531901100
Subject(s) - epidermis (zoology) , wound healing , epidermal growth factor , microbiology and biotechnology , regeneration (biology) , in vivo , anatomy , chemistry , biology , immunology , cell culture , genetics
We report here the identification of an angiopoietin-related growth factor (AGF). To examine the biological function of AGF in vivo, we created transgenic mice expressing AGF in epidermal keratinocytes (K14-AGF). K14-AGF mice exhibited swollen and reddish ears, nose and eyelids. Histological analyses of K14-AGF mice revealed significantly thickened epidermis and a marked increase in proliferating epidermal cells as well as vascular cells in the skin compared with nontransgenic controls. In addition, we found rapid wound closure in the healing process and an unusual closure of holes punched in the ears of K14-AGF mice. Furthermore, we observed that AGF is expressed in platelets and mast cells, and detected at wounded skin, whereas there was no expression of AGF detected in normal skin tissues, suggesting that AGF derived from these infiltrated cells affects epidermal proliferation and thereby plays a role in the wound healing process. These findings demonstrate that biological functions of AGF in epidermal keratinocytes could lead to novel therapeutic strategies for wound care and epidermal regenerative medicine.

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