4-Methylenesterols from Theonella swinhoei sponge are natural pregnane-X-receptor agonists and farnesoid-X-receptor antagonists that modulate innate immunity

被引:42
作者
De Marino, Simona [1 ]
Ummarino, Raffaella [1 ]
D'Auria, Maria Valeria [1 ]
Chini, Maria Giovanna [2 ]
Bifulco, Giuseppe [2 ]
D'Amore, Claudio [3 ]
Renga, Barbara [3 ]
Mencarelli, Andrea [3 ]
Petek, Sylvain [4 ]
Fiorucci, Stefano [3 ]
Zampella, Angela [1 ]
机构
[1] Univ Naples Federico II, Dipartimento Chim Sostanze Nat, Via D Montesano 49, I-80131 Naples, Italy
[2] Univ Salerno, Dipartimento Sci Farmaceut & Biomed, I-84084 Fisciano, SA, Italy
[3] Univ Perugia, Dipartimento Med Clin & Sperimentale, Nuova Fac Med & Chirurg, I-06132 Perugia, Italy
[4] Polynesian Res Ctr Isl Biodivers, IRD, F-98713 Papeete, Tahiti, France
关键词
Marine sponge; Theonella swinhoei; Nuclear receptors; Farnesoid-X-receptor; Pregnane-X-receptor; CHOLESTATIC LIVER-DISEASE; PRIMARY BILIARY-CIRRHOSIS; BILE-ACID; MARINE SPONGE; URSODEOXYCHOLIC ACID; CRYSTAL-STRUCTURE; STEROLS; PXR; RIFAXIMIN; INHIBITION;
D O I
10.1016/j.steroids.2012.01.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report the isolation and the structural elucidation of a family of polyhydroxylated steroids from the marine sponge Theonella swinhoei. Decodification of interactions of these family with nuclear receptors shows that these steroids are potent agonists of human pregnane-X-receptor (PXR) and antagonists of human farnesoid-X-receptor (FXR) with the putative binding mode to nuclear receptors (NRs) obtained through docking experiments. By using monocytes isolated from transgenic mice harboring hPXR. we demonstrated that swinhosterol B counter-regulates induction of pro-inflammatory cytokines in a PXR-dependent manner. Exposure of CD4(+) T cells to swinhosterol B upregulates the expression of IL-10 causing a shift toward a T cells regulatory phenotype in a PXR dependent manner. These results pave the way to development of a dual PXR agonist/FXR antagonist with a robust immunomodulatory activity and endowed with the ability to modulate the expression of bile acid-regulated genes in the liver. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:484 / 495
页数:12
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