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Keratinocyte Growth Factor-2 on the Proliferation of Corneal Epithelial Stem Cells in Rabbit Alkali Burned Cornea 被引量:2

Keratinocyte Growth Factor-2 on the Proliferation of Corneal Epithelial Stem Cells in Rabbit Alkali Burned Cornea
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摘要 Purpose: To determine whether the topical application of keratinocyte growth factor-2 (KGF-2) can enhance corneal epithelial healing in rabbit alkali burned cornea. In addition, the distribution and proliferation of corneal epithelial stem cells in KGF-2-treated and control corneas were investigated to explain their mechanisms of effects on the epithelium. Methods: Twenty-four New Zealand eyes were divided into four groups, treated with KGF-2 solution (1, 50, 100 μg/ml) and PBS solution. Eighth millimeter filter paper discs, produced by standard paper punch, were soaked for 15 sec in 0.5N NaOH solution. The alkali-soaked discs were applied to the central cornea, centered on the pupil and held gently in position with forceps for 1 min. The cornea was finally irrigated over 1 min with 100 ml balanced salt solution (BSS). Keratinocyte growth factor-2 was then applied topically three times a day. The phosphate-buffered saline (PBS) group was served as a control. Each corneal epithelial defect was subsequently photographed every 24 hours with a slit lamp and was measured by computer-assisted digitizer. In each group, two rabbits were sacrificed for light microscopic examination after the interval of 7, 14 and 21 days. Meanwhile, the cornea epithelium was examined by immunohistochemistry for P63, AE5, EGFR. Results: Topical application of 10 μg/ml to 100 μg/ml KGF-2 significantly accelerated corneal epithelial wound healing when compared with controls. After 24 hours, epithelial healing rate of the 100 μg/ml KGF-2 group and the PBS treated group was (74±6)% and (40±8)% (P < 0.05). After 48 hours, the rate of the C group was (94±6)%, whereas in the control group it was (73±12)% (P < 0.05). Epithelial defects were often recurrent, which happened only two times in the 100 μg/ml KGF-2-treated group, but many times in the control group. In the corneal epithelial stem cell analysis, the number of the P63 positive cells was higher in the KGF-2-treated corneal epithelium than in the controls. The P63 positive cells in Purpose: To determine whether the topical application of keratinocyte growth factor-2 (KGF-2) can enhance corneal epithelial healing in rabbit alkali burned cornea. In addition, the distribution and proliferation of corneal epithelial stem cells in KGF-2- treated and control corneas were investigated to explain their mechanisms of effects on the epithelium. Methods: Twenty-four New Zealand eyes were divided into four groups, treated with KGF-2 solution ( 1, 50, 100 μg/ml) and PBS solution. Eighth millimeter filter paper discs, produced by standard paper punch, were soaked for 15 see in 0.5N NaOH solution. The alkali-soaked discs were applied to the central cornea, centered on the pupil and held gently in position with forceps for 1 min. The cornea was finally irrigated over 1 min with 100 ml balanced salt solution (BSS). Keratinocyte growth factor-2 was then applied topically three times a day. The phosphate-buffered saline (PBS) group was served as a control. Each corneal epithelial defect was subsequently photographed every 24 hours with a slit lamp and was measured by computer-assisted digitizer. In each group, two rabbits were sacrificed for light microscopic examination after the interval of 7, 14 and 21 days. Meanwhile, the cornea epithelium was examined by immunohistochemistry for P63, AE5, EGFR. Results : Topical application of 10 μg/ml to 100μg/ml KGF-2 significantly accelerated corneal epithelial wound healing when compared with controls. After 24 hours, epithelial healing rate of the 100 μg/ml KGF-2 group and the PBS treated group was (74±6)% and (40±8)% (P 〈 0.05). After 48 hours, the rate of the C group was (94±6)%, whereas in the control group it was (73±12)% (P 〈 0.05). Epithelial defects were often recurrent, which happened only two times in the 100μg/ml KGF- 2-treated group, but many times in the control group. In the corneal epithelial stem cell analysis, the number of the P63 positive cells was higher in the KGF-2-treated corneal epi
出处 《眼科学报》 2007年第2期107-116,共10页 Eye Science
基金 National Natural Science Foundation of China ( No.39870801) Special Purpose Original New Drug Foundationin Technology Domain of Guangzhou (No.2006Z3-E4091) Medical Technique Foundation of Guangdong Province (No. B2006118) .
关键词 角化细胞生长因子-2 角膜上皮干细胞 角膜碱烧伤 治疗 细胞培养 Corneal epithelial stem cells P63 Kerationcyte growth factor-2 Cornealalkali injure
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参考文献16

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同被引文献9

  • 1Abler LL, Mansour SL, Sun X. Conditional gene inactivation reveals roles for FGF-10 and FGF-2 in establishing a normal pattern of epithelial branching in the mouse lung [J]. Dev Dyn, 2009, 238: 1999-2013. 被引量:1
  • 2Hamady ZZ, Scott N, Farrar MD, et al. Xylan regulated delivery of human keratinocyte growth factor-2 to the inflammed colon by the human anaerobic commensal bacterium Bacteroides ovatus[J]. Gut, 2010, 59: 461-469. 被引量:1
  • 3Phoenix TN, Temple S. Baby got brain: FGF10 sets rostral cortical size [ J ]. Neuron, 2009, 63 : 1-3. 被引量:1
  • 4Steiling H, Werner S. Fibroblast growth factors, key players in epithelial morphogenesis, repair and eytoproteetion [J]. Curr Opin Biotechnol, 2003, 14: 533-537. 被引量:1
  • 5Radek KA, Taylor KR, Gallo RL. FGF-10 and specific structural elements of dermatan sulfate size and sulfation promote maximal keratinocyte migration and cellular proliferation [ J ]. Wound Repair Regen, 2009, 17 : 118-126. 被引量:1
  • 6Dieckgraefe BK, Korzenik JR, Anant S. Growth factors as treatment options for intestinal inflammation[ J]. Ann N Y Acad Sci, 2006, 1072: 300-306. 被引量:1
  • 7Zhang X, Wu M, Zhang W, et al. Differentiation of human adipose-derived stem cells induced by recombinantly expressed fibroblast growth factor 10 in vitro and in vivo [J]. In Vitro Cell Dev Biol, 2010, 46: 60-71. 被引量:1
  • 8Gupte VV, Ramasamy SK, Reddy R, et al. Overexpression of fibroblast growth factor 10 (FGF-10) both during the inflammatory and the fibrotic phases attenuates bleomycin-Iinduced pulmonary fibrosis in mice [ J]. Am J Respir Crit Care Med, 2009, 180: 424-436. 被引量:1
  • 9高荣莲,马萍,陈鹏,梁洁,王丽峰,肖瑞,康宏向,杨艳峰,钱焕文,王玉芝.角质细胞生长因子-2对角膜激光烧伤的治疗作用及机制研究[J].中国激光医学杂志,2010,19(4):205-209. 被引量:5

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