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瘦素对体外大鼠成纤维细胞增殖与胶原合成的影响
引用本文:李培兵,金宏,刘佃辛,王先远,许志勤,南文考,王永辉,高兰兴.瘦素对体外大鼠成纤维细胞增殖与胶原合成的影响[J].中国修复重建外科杂志,2005,19(1):20-22.
作者姓名:李培兵  金宏  刘佃辛  王先远  许志勤  南文考  王永辉  高兰兴
作者单位:军事医学科学院卫生学环境医学研究所,天津,300050
基金项目:国家自然科学基金资助项目 (30 371 384)~~
摘    要:目的 研究瘦素对体外培养大鼠成纤维细胞 (fibroblast,FB)增殖与胶原合成的影响 ,以阐明 FB介导瘦素在大鼠皮肤创伤愈合中的促进作用。 方法 体外培养乳鼠真皮 FB,通过 MTT比色分析法、3H-胸腺嘧啶核苷(3H- Td R)和 3H-脯氨酸 (3H- Pro)掺入法观察不同浓度的瘦素 ,分别为 0、10、5 0、10 0、2 0 0及 4 0 0 ng/ ml对其增殖和胶原合成的影响。 结果 瘦素剂量在 4 0 0 ng/ ml以下时 ,随瘦素剂量增加明显增加了体外培养大鼠 FB MTT的光密度值和 3H- Td R的掺入量。3H- Pro的掺入量随瘦素剂量增加基本呈增大趋势。 2 0 0、4 0 0 ng/ ml剂量组的3H- Td R掺入量 379±10 1cpm、32 6± 33cpm,与对照组 2 19± 5 6 cpm比较有统计学差异 (P<0 .0 5 ) ;且 2 0 0、4 0 0 ng/ ml剂量组的 MTT吸光度(A)值 0 .0 82± 0 .0 13、0 .0 91± 0 .0 18与对照组 0 .0 6 3± 0 .0 10比较有统计学差异 (P<0 .0 5 ) ;2 0 0、4 0 0 ng/ ml剂量组的 3H- Pro掺入量 911± 5 5 cpm、10 72± 2 5 9cpm,与对照组 6 79± 176 cpm比较有统计学差异 (P<0 .0 5 )。 结论 瘦素促进了 FB的增殖和胶原蛋白的合成 ,这可能是瘦素发挥促进大鼠皮肤愈合作用的途径之一。

关 键 词:瘦素  大鼠  胶原合成  增殖  剂量  FB  对照组  鼠成纤维细胞  体外培养  脯氨酸
修稿时间:2004年1月16日

STUDY ON THE EFFECT OF LEPTIN ON FIBROBLAST PROLIFERATION AND COLLAGEN SYNTHESIS IN VITRO IN RATS
LI Peibing,JIN Hong,LIU Dianxin,et al..STUDY ON THE EFFECT OF LEPTIN ON FIBROBLAST PROLIFERATION AND COLLAGEN SYNTHESIS IN VITRO IN RATS[J].Chinese Journal of Reparative and Reconstructive Surgery,2005,19(1):20-22.
Authors:LI Peibing  JIN Hong  LIU Dianxin  
Institution:Institution of Hygiene and Environmental Medicine, Academy of Military Medical Sciences, Tianjin 300050, P R China. lipibing@sohu.com
Abstract:OBJECTIVE: To investigate the effect of leptin on fibroblast proliferation and collagen synthesis as to elucidate that fibroblasts play a role in leptin's effect on wound healing. METHODS: Purified dermal fibroblasts were derived from sucking wistar rat skin and exposed to leptin at concentration of 0, 10, 50, 100, 200, and 400 ng/ml. The survived fibroblasts were assessed by the colorimetric thiazolyl blue (MTT) assay. Replication of fibroblast was quantified by the incorporation of 3H-thymidine. Collagen synthesis of fibroblast cell was measured by the incorporation of 3H-proline into collagenase-sensitive protein. RESULTS: The absorption of fibroblast exposed to leptin at concentration of 200 and 400 ng/ml 0.082 +/- 0.013, 0.091 +/- 0.018 was higher than that of control group 0.063 +/- 0.010, P < 0.05. The incorporations of 3H-thymidine of fibroblast exposed to leptin at concentration of 200 and 400 ng/ml 379 +/- 101 cpm, 326 +/- 33 cpm were significantly higher than those of control group 219 +/- 56 cpm, P < 0.05. The incorporations of 3H-proline of fibroblast exposed to leptin at concentration of 200 and 400 ng/ml 911 +/- 55 cpm, 1 072 +/- 259 cpm were significantly higher than that of control group 679 +/- 176 cpm, P < 0.05. CONCLUSION: Lepin can promote rat cutaneous fibroblast proliferation and collagen synthesis in vitro. This suggests that cutaneous fibroblast plays a role in leptin's promoting skin wound healing and it may be one of the main mechanisms by which leptin enhances skin wound healing.
Keywords:Leptin    Fibroblast    Collagen    Proliferation    Wound healing
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