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罗沙司他类似物挽救了细胞模型中内质网滞留的 ABCB4 变异体的细胞内运输和功能。

Structural analogues of roscovitine rescue the intracellular traffic and the function of ER-retained ABCB4 variants in cell models.

机构信息

Inserm, Sorbonne Université, Centre de Recherche Saint-Antoine (CRSA), UMR_S 938, Institute of Cardiometabolism and Nutrition (ICAN), F-75012, Paris, France.

ManRos Therapeutics, Hôtel de Recherche, Centre de Perharidy, F-29680, Roscoff, France.

出版信息

Sci Rep. 2019 Apr 30;9(1):6653. doi: 10.1038/s41598-019-43111-y.

DOI:10.1038/s41598-019-43111-y
PMID:31040306
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6491434/
Abstract

Adenosine triphosphate binding cassette transporter, subfamily B member 4 (ABCB4) is the transporter of phosphatidylcholine at the canalicular membrane of hepatocytes. ABCB4 deficiency, due to genetic variations, is responsible for progressive familial intrahepatic cholestasis type 3 (PFIC3) and other rare biliary diseases. Roscovitine is a molecule in clinical trial that was shown to correct the F508del variant of cystic fibrosis transmembrane conductance regulator (CFTR), another ABC transporter. In the present study, we hypothesized that roscovitine could act as a corrector of ABCB4 traffic-defective variants. Using HEK and HepG2 cells, we showed that roscovitine corrected the traffic and localisation at the plasma membrane of ABCB4-I541F, a prototypical intracellularly retained variant. However, roscovitine caused cytotoxicity, which urged us to synthesize non-toxic structural analogues. Roscovitine analogues were able to correct the intracellular traffic of ABCB4-I541F in HepG2 cells. Importantly, the phospholipid secretion activity of this variant was substantially rescued by three analogues (MRT2-235, MRT2-237 and MRT2-243) in HEK cells. We showed that these analogues also triggered the rescue of intracellular traffic and function of two other intracellularly retained ABCB4 variants, i.e. I490T and L556R. Our results indicate that structural analogues of roscovitine can rescue genetic variations altering the intracellular traffic of ABCB4 and should be considered as therapeutic means for severe biliary diseases caused by this class of variations.

摘要

三磷酸腺苷结合盒转运体 B 亚家族成员 4(ABCB4)是肝细胞胆小管膜上的磷脂酰胆碱转运体。由于基因突变,ABCB4 缺乏可导致进行性家族性肝内胆汁淤积症 3 型(PFIC3)和其他罕见的胆道疾病。罗沙司他是一种正在临床试验中的分子,已被证明可纠正囊性纤维化跨膜电导调节因子(CFTR)的 F508del 变体,CFTR 也是一种 ABC 转运体。在本研究中,我们假设罗沙司他可以作为 ABCB4 转运缺陷变异体的校正剂。使用 HEK 和 HepG2 细胞,我们表明罗沙司他纠正了 ABCB4-I541F 的转运和质膜定位,ABCB4-I541F 是一种典型的细胞内滞留变体。然而,罗沙司他引起了细胞毒性,这促使我们合成非毒性结构类似物。罗沙司他类似物能够纠正 HepG2 细胞中 ABCB4-I541F 的细胞内转运。重要的是,这一变体的磷脂分泌活性被三种类似物(MRT2-235、MRT2-237 和 MRT2-243)在 HEK 细胞中显著挽救。我们表明,这些类似物还触发了两种其他细胞内滞留的 ABCB4 变体,即 I490T 和 L556R 的细胞内转运和功能的挽救。我们的结果表明,罗沙司他的结构类似物可以挽救改变 ABCB4 细胞内转运的遗传变异,并且应该被视为由这类变异引起的严重胆道疾病的治疗手段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6a8/6491434/82d951a80add/41598_2019_43111_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6a8/6491434/e3be802d68a5/41598_2019_43111_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6a8/6491434/eb1f17375d61/41598_2019_43111_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6a8/6491434/0f76460ce97d/41598_2019_43111_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6a8/6491434/9ccc9d8380f9/41598_2019_43111_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6a8/6491434/7fbe408f1c2d/41598_2019_43111_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6a8/6491434/82d951a80add/41598_2019_43111_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6a8/6491434/e3be802d68a5/41598_2019_43111_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6a8/6491434/eb1f17375d61/41598_2019_43111_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6a8/6491434/0f76460ce97d/41598_2019_43111_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6a8/6491434/9ccc9d8380f9/41598_2019_43111_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6a8/6491434/7fbe408f1c2d/41598_2019_43111_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6a8/6491434/82d951a80add/41598_2019_43111_Fig6_HTML.jpg

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