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过氧化物酶体增殖物激活受体 γ 调控的组织蛋白酶 D 是树突状细胞呈递脂质抗原所必需的。

Peroxisome proliferator-activated receptor γ-regulated cathepsin D is required for lipid antigen presentation by dendritic cells.

机构信息

Department of Biochemistry and Molecular Biology, Research Center for Molecular Medicine, University of Debrecen, Debrecen 4010, Hungary.

出版信息

J Immunol. 2011 Jul 1;187(1):240-7. doi: 10.4049/jimmunol.1002421. Epub 2011 Jun 1.

Abstract

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.

摘要

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。

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