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In vivo characterization of keratinocyte growth factor‐2 as a potential wound healing agent
Author(s) -
Soler Pedro M,
Wright Terry E,
Smith Paul D,
Maggi Sergio P,
Hill Donald P,
Ko Francis,
Jimenez Pablo A,
Robson Martin C
Publication year - 1999
Publication title -
wound repair and regeneration
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.847
H-Index - 109
eISSN - 1524-475X
pISSN - 1067-1927
DOI - 10.1046/j.1524-475x.1999.00172.x
Subject(s) - keratinocyte , keratinocyte growth factor , wound healing , growth factor , granulation tissue , medicine , in vivo , immunology , surgery , chemistry , in vitro , biology , receptor , biochemistry , microbiology and biotechnology
Human keratinocyte growth factor‐2 exerts a proliferative effect on epithelial cells and mediates keratinocyte migration. It has also been shown to increase both deposition of granulation tissue and collagen and maturation of collagen. Because these properties should affect the healing trajectory of wounds, this study set out to investigate the effects of keratinocyte growth factor‐2 on the healing of three different types of wounds. Human meshed skin grafts explanted to athymic “nude” rats, surgical incisions in Sprague‐Dawley rats, and acute excisional rat wounds inoculated with Escherichia coli were used. Two concentrations of recombinant human keratinocyte growth factor‐2 were compared to a vehicle control and keratinocyte growth factor‐1. Keratinocyte growth factor‐2 significantly accelerated the rate of epithelialization in the meshed skin graft model and effected a modestly more rapid gain in breaking strength of surgical incisions than keratinocyte growth factor‐1 or the vehicle control treatment. Neither keratinocyte growth factors accelerated wound closure by contraction of the excisional wounds. Based on these data, keratinocyte growth factor‐2 may be useful in accelerating healing in wounds healing mainly by the process of epithelialization such as venous stasis ulcers, partial thickness burn wounds, and skin graft donor sites. It might also accelerate the gain in incisional wound strength in acute surgical or traumatic wounds.

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