Rivier M, Castiel I, Safonova I, Ailhaud G, Michel S
GALDERMA R&D, Sophia-Antipolis cedex, Valbonne, France.
J Invest Dermatol. 2000 Apr;114(4):681-7. doi: 10.1046/j.1523-1747.2000.00939.x.
Peroxisome proliferator-activated receptors are involved in certain cell types such as adipocytes and hepatocytes, in the control of several pathways of lipid synthesis or catabolism by regulating the gene expression level of key lipid metabolizing enzymes. As the epidermis exhibits an extensive lipid metabolism necessary for the establishment of the barrier function, we have examined the role of peroxisome proliferator-activated receptor-alpha activation in this process. Living skin equivalents were treated with Wy 14,643, a selective peroxisome proliferator- activated receptor-alpha ligand, which enhanced greatly the synthesis of membrane coating granules, the organelles specialized in the processing of stratum corneum lipids. Also, the overall stratum corneum neutral lipid content assessed by Oil red O staining was increased. A detailed analysis of the lipid species present in the reconstructed epidermis showed that peroxisome proliferator-activated receptor-alpha activation increased the synthesis of ceramides and cholesterol derivatives, thought to be essential structural components of the permeability barrier. A synergistic effect was observed on lipid synthesis when peroxisome proliferator-activated receptor-alpha and retinoid X receptor were simultaneously activated by selective ligands. Furthermore, activation of peroxisome proliferator-activated receptor-alpha led to increased mRNA expression of several key enzymes of ceramide and cholesterol metabolism. An increase of serine-palmitoyl transferase and of beta-glucocerebrosidase enzymatic activity was also demonstrated. Altogether, these results show that peroxisome proliferator-activated receptor-alpha is a key transcription factor involved in the control of the epidermal lipid barrier.
过氧化物酶体增殖物激活受体参与某些细胞类型,如脂肪细胞和肝细胞,通过调节关键脂质代谢酶的基因表达水平来控制脂质合成或分解的多种途径。由于表皮表现出建立屏障功能所必需的广泛脂质代谢,我们研究了过氧化物酶体增殖物激活受体α激活在此过程中的作用。用Wy 14,643(一种选择性过氧化物酶体增殖物激活受体α配体)处理活皮肤替代物,这极大地增强了膜被颗粒的合成,膜被颗粒是专门处理角质层脂质的细胞器。此外,通过油红O染色评估的角质层总体中性脂质含量增加。对重建表皮中存在的脂质种类的详细分析表明,过氧化物酶体增殖物激活受体α激活增加了神经酰胺和胆固醇衍生物的合成,这些被认为是渗透屏障的重要结构成分。当过氧化物酶体增殖物激活受体α和视黄醇X受体被选择性配体同时激活时,在脂质合成上观察到协同效应。此外,过氧化物酶体增殖物激活受体α的激活导致神经酰胺和胆固醇代谢的几种关键酶的mRNA表达增加。还证明了丝氨酸-棕榈酰转移酶和β-葡萄糖脑苷脂酶活性的增加。总之,这些结果表明过氧化物酶体增殖物激活受体α是参与控制表皮脂质屏障的关键转录因子。