GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR AND GRANULOCYTE-COLONY-STIMULATING FACTOR - DIFFERENTIAL ACTION ON INCISIONAL WOUND-HEALING

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作者
JYUNG, RW
WU, LC
PIERCE, GF
MUSTOE, TA
机构
[1] WASHINGTON UNIV, SCH MED, DEPT OTOLARYNGOL, ST LOUIS, MO 63110 USA
[2] NORTHWESTERN UNIV, SCH MED, DIV PLAST SURG, CHICAGO, IL 60614 USA
[3] AMGEN INC, DEPT EXPTL PATHOL, THOUSAND OAKS, CA 91320 USA
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R61 [外科手术学];
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摘要
Background. Granulocyte-macrophage colony-stimulating factor (GM-CSF) specifically stimulates granulocyte, macrophage, and eosinophil colonies; granulocyte colony-stimulating factor (G-CSF) acts directly on neutrophil-restricted progenitor cells in their proliferation. Those cells have been implicated in the process of wound healing. Methods. Paired 6 cm incisions were made on rats; GM-CSF or G-CSF was given systemically (100 mu g/kg/dose) or locally 30 mu g/wound). The controls received vehicle alone. Impaired healing was induced by injection of methylprednisolone (30 mg/kg). White blood cells (WBC) were counted at day 2 after treatment. Tissue strips were evaluated for tensiometry and histologic features at days 7 and 14 after wounding. Results. For local GM-CSF treated incisions, the breaking strength was 25% stronger than controls at day 7 (p = 0.004), 36% at day 14 (p < 0.0001), and 42% at day 7 (p = 0.012) in impaired animals. Local G-CSF and systemic GM-CSF and G-CSF increased circulating WBC (p < 0.05), but they had no effects on healing. Histologic studies revealed an increase of wound cellulity at day 7 and day 14 in topical GM-CSF treated wounds. Conclusions. These results suggest GM-CSF is an activator of tissue macrophages and that increasing circulating WBC did not affect wound healing.
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页码:325 / 334
页数:10
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