Zhao Jing, Tian Tian, Zhang Qiong, Wang Yonggang, Li Yanping
Reproductive Medicine Center, Xiangya Hospital, Central South University, Changsha, Hunan, China.
PLoS One. 2013 Dec 23;8(12):e82375. doi: 10.1371/journal.pone.0082375. eCollection 2013.
Granulocyte colony-stimulating factor (G-CSF) induces stem cells to mobilize to the injury site, which have beneficial effect on tissue repair. The aim of this study was to investigate the effect of G-CSF on the thin endometrium in rat models. In the present study, rats with thin endometrium were divided into 4 groups (experimental group I: administrated with G-CSF (40 µg/kg/d) 4-6 hours post-modeling; control group I: administrated with saline 4-6 hours post-modeling; experimental group II: administrated with G-CSF (40 µg/kg/d) 12 days post-modeling; control group II: administrated with saline 12 days post-modeling. The agentia was given once daily and last for 5 days. Endometrial morphology was analyzed by Hematoxylin-Eosin staining, and the regeneration of endometrial cells was evaluated by immunohistochemistry and western-blot with cytokeratin and vimentin. We found that endometrial thickness and morphology presented a significant difference between experimental groups and control groups. No matter when we start with G-CSF, there was a significantly thicker endometrium and stronger expression of cytokeratin/vimintin in the experimental groups compared with the control groups (P<0.01). There were significant thicker endometrial lining and stronger expression of cytokeratin/vimintin in experimental group I than that of experimental group II (P<0.05), but there was no difference in the endometrial lining and the expression of cytokeratin/vimintin between the two control groups (P>0.05). In conclusion, G-CSF can promote the regeneration of endometrial cells in animal research, especially when the G-CSF was administrated earlier.
粒细胞集落刺激因子(G-CSF)可诱导干细胞向损伤部位动员,这对组织修复具有有益作用。本研究旨在探讨G-CSF对大鼠薄型子宫内膜模型的影响。在本研究中,将薄型子宫内膜大鼠分为4组(实验组I:建模后4 - 6小时给予G-CSF(40μg/kg/d);对照组I:建模后4 - 6小时给予生理盐水;实验组II:建模后12天给予G-CSF(40μg/kg/d);对照组II:建模后12天给予生理盐水。药物每日给药1次,持续5天。通过苏木精-伊红染色分析子宫内膜形态,并用细胞角蛋白和波形蛋白的免疫组织化学及蛋白质印迹法评估子宫内膜细胞的再生情况。我们发现实验组与对照组之间子宫内膜厚度和形态存在显著差异。无论何时开始给予G-CSF,与对照组相比,实验组的子宫内膜明显更厚,细胞角蛋白/波形蛋白的表达更强(P<0.01)。实验组I的子宫内膜厚度和细胞角蛋白/波形蛋白的表达明显高于实验组II(P<0.05),但两个对照组之间的子宫内膜厚度和细胞角蛋白/波形蛋白的表达无差异(P>0.05)。总之,在动物研究中,G-CSF可促进子宫内膜细胞的再生,尤其是早期给予G-CSF时。