Division of Neuroscience, Oregon National Primate Research Center, Oregon Health and Science University, Beaverton, OR, USA.
Int J Obes (Lond). 2010 Jun;34(6):989-1000. doi: 10.1038/ijo.2010.12. Epub 2010 Feb 16.
A sexual dimorphism exists in body fat distribution; females deposit relatively more fat in subcutaneous/inguinal depots whereas males deposit more fat in the intra-abdominal/gonadal depot. Our objective was to systematically document depot- and sex-related differences in the accumulation of adipose tissue and gene expression, comparing differentially expressed genes in diet-induced obese mice with mice maintained on a chow diet.
We used a microarray approach to determine whether there are sexual dimorphisms in gene expression in age-matched male, female or ovariectomized female (OVX) C57/BL6 mice maintained on a high-fat (HF) diet. We then compared expression of validated genes between the sexes on a chow diet.
After exposure to a high fat diet for 12 weeks, females gained less weight than males. The microarray analyses indicate in intra-abdominal/gonadal adipose tissue in females 1642 genes differ by at least twofold between the depots, whereas 706 genes differ in subcutaneous/inguinal adipose tissue when compared with males. Only 138 genes are commonly regulated in both sexes and adipose tissue depots. Inflammatory genes (cytokine-cytokine receptor interactions and acute-phase protein synthesis) are upregulated in males when compared with females, and there is a partial reversal after OVX, where OVX adipose tissue gene expression is more 'male-like'. This pattern is not observed in mice maintained on chow. Histology of male gonadal white adipose tissue (GWAT) shows more crown-like structures than females, indicative of inflammation and adipose tissue remodeling. In addition, genes related to insulin signaling and lipid synthesis are higher in females than males, regardless of dietary exposure.
These data suggest that male and female adipose tissue differ between the sexes regardless of diet. Moreover, HF diet exposure elicits a much greater inflammatory response in males when compared with females. This data set underscores the importance of analyzing depot-, sex- and steroid-dependent regulation of adipose tissue distribution and function.
体脂分布存在性别二态性;女性在皮下/腹股沟部位储存相对较多的脂肪,而男性则在腹部/性腺部位储存较多的脂肪。我们的目的是系统地记录脂肪组织和基因表达的储存和性别差异,比较饮食诱导肥胖的雄性和雌性小鼠以及维持正常饮食的雄性和雌性小鼠的差异表达基因。
我们使用微阵列方法来确定在年龄匹配的雄性、雌性或去卵巢雌性(OVX)C57/BL6 小鼠中,是否存在高脂肪(HF)饮食下基因表达的性别二态性。然后,我们比较了雌雄激素在正常饮食下的表达。
暴露于高脂肪饮食 12 周后,雌性体重增加少于雄性。微阵列分析表明,在雌性的腹部/性腺脂肪组织中,1642 个基因在两个部位之间的差异至少为两倍,而在皮下/腹股沟脂肪组织中,与雄性相比,有 706 个基因存在差异。只有 138 个基因在两性和脂肪组织中都受到共同调控。与雌性相比,雄性的炎症基因(细胞因子-细胞因子受体相互作用和急性期蛋白合成)上调,而 OVX 后则部分逆转,OVX 脂肪组织的基因表达更“男性化”。这种模式在维持正常饮食的小鼠中没有观察到。雄性性腺白色脂肪组织(GWAT)的组织学显示出比雌性更多的冠层结构,表明存在炎症和脂肪组织重塑。此外,无论饮食暴露如何,与雄性相比,雌性的胰岛素信号和脂质合成相关基因更高。
无论饮食如何,雄性和雌性脂肪组织在两性之间存在差异。此外,与雌性相比,HF 饮食暴露会在雄性中引起更大的炎症反应。本数据集强调了分析脂肪组织分布和功能的储存、性别和类固醇依赖性调节的重要性。