Kadegowda Anil K G, Khan M Jawad, Piperova Liliana S, Teter Beverly B, Rodriguez-Zas Sandra L, Erdman Richard A, Loor Juan J
Department of Animal and Avian Sciences, University of Maryland, College Park, MD 20742, USA.
J Lipids. 2013;2013:890343. doi: 10.1155/2013/890343. Epub 2013 May 14.
Exogenous trans-10, cis-12-CLA (CLA) reduces lipid synthesis in murine adipose and mammary (MG) tissues. However, genomewide alterations in MG and liver (LIV) associated with dietary CLA during lactation remain unknown. We fed mice (n = 5/diet) control or control + trans-10, cis-12-CLA (37 mg/day) between d 6 and d 10 postpartum. The 35,302 annotated murine exonic evidence-based oligo (MEEBO) microarray and quantitative RT-PCR were used for transcript profiling. Milk fat concentration was 44% lower on d 10 versus d 6 due to CLA. The CLA diet resulted in differential expression of 1,496 genes. Bioinformatics analyses underscored that a major effect of CLA on MG encompassed alterations in cellular signaling pathways and phospholipid species biosynthesis. Dietary CLA induced genes related to ER stress (Xbp1), apoptosis (Bcl2), and inflammation (Orm1, Saa2, and Cp). It also induced marked inhibition of PPAR γ signaling, including downregulation of Pparg and Srebf1 and several lipogenic target genes (Scd, Fasn, and Gpam). In LIV, CLA induced hepatic steatosis probably through perturbations in the mitochondrial functions and induction of ER stress. Overall, results from this study underscored the role of PPAR γ signaling on mammary lipogenic target regulation. The proinflammatory effect due to CLA could be related to inhibition of PPAR γ signaling.
外源性反式-10,顺式-12-共轭亚油酸(CLA)可减少小鼠脂肪组织和乳腺组织中的脂质合成。然而,哺乳期饮食中CLA所导致的乳腺和肝脏全基因组变化仍不清楚。我们在产后第6天至第10天给小鼠(每组n = 5)喂食对照饮食或对照饮食 + 反式-10,顺式-12-CLA(37毫克/天)。采用35,302个注释的基于小鼠外显子的证据寡核苷酸(MEEBO)微阵列和定量逆转录-聚合酶链反应进行转录谱分析。由于CLA的作用,第10天的乳脂肪浓度比第6天降低了44%。CLA饮食导致1,496个基因的差异表达。生物信息学分析强调,CLA对乳腺的主要影响包括细胞信号通路和磷脂种类生物合成的改变。饮食中的CLA诱导了与内质网应激(Xbp1)、细胞凋亡(Bcl2)和炎症(Orm1、Saa2和Cp)相关的基因。它还显著抑制了PPARγ信号通路,包括Pparg和Srebf1以及几个脂肪生成靶基因(Scd、Fasn和Gpam)的下调。在肝脏中,CLA可能通过干扰线粒体功能和诱导内质网应激而导致肝脂肪变性。总体而言,本研究结果强调了PPARγ信号通路在乳腺脂肪生成靶标调节中的作用。CLA引起的促炎作用可能与PPARγ信号通路的抑制有关。