首页|VEGF对小鼠卵巢类固醇合成相关基因表达的影响及其机制

VEGF对小鼠卵巢类固醇合成相关基因表达的影响及其机制

扫码查看
目的 探讨血管内皮生长因子(VEGF)对小鼠卵巢类固醇合成相关基因表达的影响及其机制。方法 利用四环素可逆调节VEGF表达的转基因小鼠模型,采用聚合酶链反应(PCR)法鉴定小鼠基因型,通过喂食强力霉素将20只小鼠分为VEGF表达正常组(Dox+)与VEGF表达抑制组(Dox-)(n=10)。采用Western blotting检测卵巢组织中VEGF蛋白的表达情况;荧光定量PCR检测VEGF、VEGF受体2(KDR)及已知在卵泡发育中发挥作用的基因卵泡刺激素(FSH)、抑制素B(INHBB)mRNA的表达情况。HE染色观察卵巢组织的变化。取小鼠卵巢组织提取总RNA进行转录组测序,并通过FPKM、log2FC值分析相关差异基因。结果 与Dox+组比较,Dox-组VEGF mRNA和蛋白水平明显降低,KDR mRNA水平明显降低(P<0。05)。HE染色结果显示,与Dox+组比较,Dox-组卵泡发育障碍,并出现闭锁卵泡。根据测序结果分析筛选出两组小鼠的卵泡发育相关基因、类固醇合成相关基因具有明显差异(P<0。05);富集分析发现小鼠卵巢中VEGF主要参与调控卵巢类固醇生成等通路。荧光定量PCR结果显示,与Dox+组相比,Dox-组小鼠卵巢组织中卵泡发育相关基因(INHBB、FSHR)明显上调(P<0。05),类固醇合成的关键基因(StAR、CYP11A1、3β-HSD)明显下调(P<0。05),定量结果与测序结果基本一致。结论 VEGF抑制可使小鼠卵泡发育障碍,其可能的机制是通过下调卵巢类固醇合成相关基因FSH、INHBB的表达从而阻碍胆固醇代谢来实现的。
Effect of VEGF on the expression of genes related to ovarian steroid synthesis in mice and its mechanism
Objective To investigate the effect of vascular endothelial growth factor(VEGF)on the expression of genes related to ovarian steroid synthesis in mice and its underlying mechanism.Methods A transgenic mouse model with tetracycline-reversible regulation of VEGF expression was used,and the genotype of mice was identified by polymerase chain reaction(PCR).Twenty mice were divided into normal VEGF expression group(Dox+,n=10)and VEGF expression inhibition group(Dox-,n=10)by feeding them doxycycline.Western blotting was used to detect the expression of VEGF protein in ovarian tissues.Fluorescence quantitative PCR was used to detect the mRNA expression of VEGF,KDR and genes known to play roles in follicle development,such as follicle-stimulating hormone(FSH)and inhibin B(INHBB).HE staining was used to observe changes in ovarian tissue.Total RNA was extracted from mouse ovarian tissues for transcriptome sequencing,and the relevant differential genes were analyzed by FPKM and log2FC values.Results Compared with the Dox+group,the mRNA and protein levels of VEGF in the Dox-group significantly reduced,and the mRNA levels of KDR also significantly decreased(P<0.05).HE staining results showed that compared with the Dox+group,follicular development was impaired and atresia follicles appeared in the Dox-group.Sequencing analysis identified that significant differences in follicular development-related genes and steroid synthesis-related genes between the two groups(P<0.05).Enrichment analysis showed that VEGF in mouse ovaries mainly regulates ovarian steroidogenesis and other pathways.Fluorescence quantitative PCR results demonstrated that compared with the Dox+group,the follicular development-related genes(INHBB and FSHR)in the ovarian tissues of the Dox-group were significantly up-regulated(P<0.05),whereas the key genes of steroid synthesis(StAR,CYP11A1,3β-HSD)were significantly down-regulated(P<0.05).The quantitative results were basically consistent with the sequencing results.Conclusion Mice with inhibited VEGF exhibited ovarian follicular dysplasia,potentially due to the mechanism whereby VEGF inhibition downregulated the expression of genes associated with steroid synthesis,such as FSH and INHBB,thereby obstructing cholesterol metabolism.

vascular endothelial growth factorfollicular developmentsexual steroid hormonestranscriptome sequencing

张智慧、高鸿霞、王国庆、侯巍、邹畅、芦小单

展开 >

吉林省人民医院精准分子医学中心,吉林长春 130000

北华大学医学技术学院,吉林省吉林市 132000

血管内皮生长因子 卵泡发育 性类固醇激素 转录组测序

吉林省自然科学基金吉林省自然科学基金项目吉林省科技厅创新团队项目

20240101007JCYDZJ202201ZYTS14820220508080RC

2024

解放军医学杂志
人民军医出版社

解放军医学杂志

CSTPCD北大核心
影响因子:1.644
ISSN:0577-7402
年,卷(期):2024.49(6)
  • 9