Angiopoietin-related growth factor (AGF) promotes epidermal proliferation, remodeling, and regeneration

被引:111
作者
Oike, Y [1 ]
Yasunaga, K
Ito, Y
Matsumoto, S
Maekawa, H
Morisada, T
Arai, F
Nakagata, N
Takeya, M
Masuho, Y
Suda, T
机构
[1] Keio Univ, Sch Med, Sakaguchi Lab, Dept Cell Differentiat, Tokyo 1608582, Japan
[2] Yamanouchi Pharmaceut Co Ltd, Mol Med Labs, Tsukuba, Ibaraki 3058585, Japan
[3] Helix Res Inst Inc, Kisarazu 2920812, Japan
[4] Kumamoto Univ, Ctr Anim Resources & Dev, Kumamoto 8600811, Japan
[5] Kumamoto Univ, Dept Pathol, Kumamoto 8600811, Japan
关键词
D O I
10.1073/pnas.1531901100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:9494 / 9499
页数:6
相关论文
共 36 条
  • [1] [Anonymous], 1994, MANIPULATING MOUSE E
  • [2] Mast cells and their mediators in cutaneous wound healing active participants or innocent bystanders?
    Artuc, M
    Hermes, B
    Steckelings, UM
    Grützkau, A
    Henz, BM
    [J]. EXPERIMENTAL DERMATOLOGY, 1999, 8 (01) : 1 - 16
  • [3] Mast cells can secrete vascular permeability factor vascular endothelial cell growth factor and exhibit enhanced release after immunoglobulin E-dependent upregulation of Fcε receptor I expression
    Boesiger, J
    Tsai, M
    Maurer, M
    Yamaguchi, M
    Brown, LF
    Claffey, KP
    Dvorak, HF
    Galli, SJ
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (06) : 1135 - 1145
  • [4] ANGPTL3 stimulates endothelial cell adhesion and migration via integrin αvβ3 and induces blood vessel formation in vivo
    Camenisch, G
    Pisabarro, MT
    Sherman, D
    Kowalski, J
    Nagel, M
    Hass, P
    Xie, MH
    Gurney, A
    Bodary, S
    Liang, XH
    Clark, K
    Beresini, M
    Ferrara, N
    Gerber, HP
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (19) : 17281 - 17290
  • [5] A new murine model for mammalian wound repair and regeneration
    Clark, LD
    Clark, RK
    Heber-Katz, E
    [J]. CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1998, 88 (01): : 35 - 45
  • [6] Detmar M, 1998, J INVEST DERMATOL, V110, P504
  • [7] DUMONT DJ, 1992, ONCOGENE, V7, P1471
  • [8] Induction of hypervascularity without leakage or inflammation in transgenic mice overexpressing hypoxia-inducible factor-1α
    Elson, DA
    Thurston, G
    Huang, LE
    Ginzinger, DG
    McDonald, DM
    Johnson, RS
    Arbeit, JM
    [J]. GENES & DEVELOPMENT, 2001, 15 (19) : 2520 - 2532
  • [9] Growth factors acting via endothelial cell-specific receptor tyrosine kinases: VEGFs, angiopoietins, and ephrins in vascular development
    Gale, NW
    Yancopoulos, GD
    [J]. GENES & DEVELOPMENT, 1999, 13 (09) : 1055 - 1066
  • [10] Keratinocyte growth factor is required for hair development but not for wound healing
    Guo, LF
    Degenstein, L
    Fuchs, E
    [J]. GENES & DEVELOPMENT, 1996, 10 (02) : 165 - 175