Li Peibing, Jin Hong, Liu Dianxin, Gao Lanxing, Xu Zhiqin, Nan Wenkao, Wang Yonghui, Gao Lanxing
Institution of Hygiene and Environmental Medicine, Academy of Military Medical Sciences, Tianjin 300050, P R China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2005 Jan;19(1):20-2.
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.
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.
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.
Leptin 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.
研究瘦素对成纤维细胞增殖及胶原合成的影响,以阐明成纤维细胞在瘦素促进伤口愈合中的作用。
从新生Wistar大鼠皮肤中分离纯化真皮成纤维细胞,分别用浓度为0、10、50、100、200和400 ng/ml的瘦素处理。采用比色法噻唑蓝(MTT)法评估存活的成纤维细胞。通过掺入3H-胸腺嘧啶核苷来定量成纤维细胞的增殖。通过将3H-脯氨酸掺入对胶原酶敏感的蛋白中来测定成纤维细胞的胶原合成。
用浓度为200和400 ng/ml瘦素处理的成纤维细胞的吸光度分别为0.082±0.013、0.091±0.018,高于对照组的0.063±0.010,P<0.05。用浓度为200和400 ng/ml瘦素处理的成纤维细胞的3H-胸腺嘧啶核苷掺入量分别为379±101 cpm、326±33 cpm,显著高于对照组的219±56 cpm,P<0.05。用浓度为200和400 ng/ml瘦素处理的成纤维细胞的3H-脯氨酸掺入量分别为911±55 cpm、1072±259 cpm,显著高于对照组的679±176 cpm,P<0.05。
瘦素在体外可促进大鼠皮肤成纤维细胞的增殖及胶原合成。这表明皮肤成纤维细胞在瘦素促进皮肤伤口愈合中发挥作用,可能是瘦素促进皮肤伤口愈合的主要机制之一。