Department of Biochemistry and Molecular Biology, Research Center for Molecular Medicine, University of Debrecen, Debrecen 4010, Hungary.
J Immunol. 2011 Jul 1;187(1):240-7. doi: 10.4049/jimmunol.1002421. Epub 2011 Jun 1.
It is well established that dendritic cells (DCs) take up, process, and present lipid Ags in complex with CD1d molecules to invariant NKT cells. The lipid-activated transcription factor, peroxisome proliferator-activated receptor γ (PPARγ), has previously been shown to regulate CD1d expression in human monocyte-derived DCs, providing a link between lipid metabolism and lipid Ag presentation. We report that PPARγ regulates the expression of a lysosomal protease, cathepsin D (CatD), in human monocyte-derived DCs. Inhibition of CatD specifically reduced the expansion of invariant NKT cells and furthermore resulted in decreased maturation of saposins, a group of lipid transfer proteins required for lysosomal lipid Ag processing and loading. These results reveal a novel mechanism of lipid Ag presentation and identify CatD as a key component of this machinery and firmly place PPARγ as the transcriptional regulator linking lipid metabolism and lipid Ag processing.
众所周知,树突状细胞(DC)摄取、加工并呈递与 CD1d 分子结合的脂质抗原给恒定自然杀伤 T 细胞。脂激活转录因子过氧化物酶体增殖物激活受体γ(PPARγ)先前已被证明可调节人单核细胞来源的树突状细胞中 CD1d 的表达,为脂质代谢和脂质抗原呈递之间提供了联系。我们报告称,PPARγ 调节人单核细胞来源的树突状细胞中溶酶体蛋白酶组织蛋白酶 D(CatD)的表达。CatD 的抑制特异性地减少了不变自然杀伤 T 细胞的扩增,并且还导致了用于溶酶体脂质抗原加工和加载的脂质转移蛋白组 saposin 的成熟减少。这些结果揭示了脂质抗原呈递的新机制,并确定 CatD 是该机制的关键组成部分,并明确将 PPARγ 作为连接脂质代谢和脂质抗原加工的转录调节剂。