Program in Integrative Nutrition and Complex Diseases, Texas A & M University, College Station, Texas 77843-2253, USA.
Am J Physiol Gastrointest Liver Physiol. 2012 Jan 1;302(1):G153-67. doi: 10.1152/ajpgi.00315.2011. Epub 2011 Sep 22.
The ligand-activated transcription factor peroxisome proliferator-activated receptor (PPAR)-δ is highly expressed in colonic epithelial cells; however, the role of PPARδ ligands, such as fatty acids, in mucosal inflammation and malignant transformation has not been clarified. Recent evidence suggests that the anti-inflammatory/chemoprotective properties of fish oil (FO)-derived n-3 polyunsaturated fatty acids (PUFAs) may be partly mediated by PPARδ. Therefore, we assessed the role of PPARδ in modulating the effects of dietary n-3 PUFAs by targeted deletion of intestinal epithelial cell PPARδ (PPARδ(ΔIEpC)). Subsequently, we documented changes in colon tumorigenesis and the inflammatory microenvironment, i.e., local [mesenteric lymph node (MLN)] and systemic (spleen) T cell activation. Animals were fed chemopromotive [corn oil (CO)] or chemoprotective (FO) diets during the induction of chronic inflammation/carcinogenesis. Tumor incidence was similar in control and PPARδ(ΔIEpC) mice. FO reduced mucosal injury, tumor incidence, colonic STAT3 activation, and inflammatory cytokine gene expression, independent of PPARδ genotype. CD8(+) T cell recruitment into MLNs was suppressed in PPARδ(ΔIEpC) mice. Similarly, FO reduced CD8(+) T cell numbers in the MLN. Dietary FO independently modulated MLN CD4(+) T cell activation status by decreasing CD44 expression. CD11a expression by MLN CD4(+) T cells was downregulated in PPARδ(ΔIEpC) mice. Lastly, splenic CD62L expression was downregulated in PPARδ(ΔIEpC) CD4(+) and CD8(+) T cells. These data demonstrate that expression of intestinal epithelial cell PPARδ does not influence azoxymethane/dextran sodium sulfate-induced colon tumor incidence. Moreover, we provide new evidence that dietary n-3 PUFAs attenuate intestinal inflammation in an intestinal epithelial cell PPARδ-independent manner.
配体激活的转录因子过氧化物酶体增殖物激活受体 (PPAR)-δ 在结肠上皮细胞中高度表达;然而,脂肪酸等 PPARδ 配体在黏膜炎症和恶性转化中的作用尚不清楚。最近的证据表明,鱼油 (FO)-衍生的 n-3 多不饱和脂肪酸 (PUFA) 的抗炎/化学保护特性可能部分由 PPARδ 介导。因此,我们通过靶向敲除肠上皮细胞 PPARδ (PPARδ(ΔIEpC)) 来评估 PPARδ 调节膳食 n-3 PUFAs 作用的能力。随后,我们记录了结肠肿瘤发生和炎症微环境的变化,即局部 [肠系膜淋巴结 (MLN)] 和全身 (脾脏) T 细胞激活的变化。在诱导慢性炎症/致癌作用期间,动物喂食化学促进 [玉米油 (CO)] 或化学保护 (FO) 饮食。对照和 PPARδ(ΔIEpC) 小鼠的肿瘤发生率相似。FO 降低了黏膜损伤、肿瘤发生率、结肠 STAT3 激活和炎症细胞因子基因表达,与 PPARδ 基因型无关。PPARδ(ΔIEpC) 小鼠中 MLN 中的 CD8(+) T 细胞募集受到抑制。同样,FO 减少了 MLN 中的 CD8(+) T 细胞数量。FO 饮食通过降低 CD44 表达独立调节 MLN CD4(+) T 细胞激活状态。PPARδ(ΔIEpC) 小鼠中 MLN CD4(+) T 细胞的 CD11a 表达下调。最后,PPARδ(ΔIEpC) CD4(+) 和 CD8(+) T 细胞的脾脏 CD62L 表达下调。这些数据表明,肠上皮细胞 PPARδ 的表达不影响氧化偶氮甲烷/葡聚糖硫酸钠诱导的结肠肿瘤发生率。此外,我们提供了新的证据表明,膳食 n-3 PUFAs 以肠上皮细胞 PPARδ 不依赖的方式减轻肠道炎症。