Hausman G J
USDA-ARS, Richard B Russell Agricultural Research Center, Animal Physiology Research Unit, 950 College Station Road, Athens, GA 30605-2720, USA.
Gen Comp Endocrinol. 2003 Aug;133(1):61-70. doi: 10.1016/s0016-6480(03)00149-7.
The present study examined the influence of dexamethasone (DEX) treatment on preadipocyte recruitment and expression of transcription factor proteins in adipose tissue stromal-vascular (S-V) cell cultures from 50 and 75 day old pig fetuses and young pigs. C/EBPalpha, C/EBPdelta, and PPARgamma immunoreactive cells had evenly reactive nuclei and unreactive nucleoli. DEX recruited many more preadipocytes in 75 day than in 50 day fetal S-V cultures. However, DEX did not increase the number of differentiated preadipocytes (lipid+, C/EBPalpha+) in 50 day S-V cultures and only slightly increased this number in 75 day fetal S-V cultures. In fetal cultures, extensive, precocious increases in C/EBPalpha expression (number of reactive cells) by day three were followed by extensive decreases in expression. However, PPARgamma expression was not expressed precociously since preadipocyte lipid accretion and PPARgamma immunoreactivity were strongly linked in fetal and pig S-V cultures. Nevertheless, all cells with lipid in fetal S-V cultures were C/EBPalpha and PPARgamma reactive. DEX increases preadipocyte differentiation in pig S-V cultures and in this study DEX increased PPARgamma expression to a much greater degree in pig than in fetal S-V cultures. These studies suggest that restricted adipogenesis in the pig fetus is attributable to limited DEX induced PPARgamma expression.
本研究检测了地塞米松(DEX)处理对来自50日龄和75日龄猪胎儿及幼猪的脂肪组织基质血管(S-V)细胞培养物中前脂肪细胞募集和转录因子蛋白表达的影响。C/EBPα、C/EBPδ和PPARγ免疫反应性细胞具有均匀反应性的细胞核和无反应性的核仁。与50日龄胎儿S-V培养物相比,DEX在75日龄胎儿的S-V培养物中募集了更多的前脂肪细胞。然而,DEX并未增加50日龄S-V培养物中分化的前脂肪细胞(脂质阳性、C/EBPα阳性)数量,而在75日龄胎儿S-V培养物中仅略微增加了该数量。在胎儿培养物中,到第三天时C/EBPα表达(反应性细胞数量)出现广泛且早熟的增加,随后表达大幅下降。然而,PPARγ表达并未早熟,因为在前脂肪细胞脂质积聚与胎儿和猪S-V培养物中的PPARγ免疫反应性之间存在强烈关联。尽管如此,胎儿S-V培养物中所有含脂质的细胞均对C/EBPα和PPARγ呈反应性。DEX增加猪S-V培养物中的前脂肪细胞分化,并且在本研究中,DEX在猪中比在胎儿S-V培养物中更大程度地增加了PPARγ表达。这些研究表明,猪胎儿脂肪生成受限归因于DEX诱导的PPARγ表达有限。