Martovetsky Gleb, Bush Kevin T, Nigam Sanjay K
Department of Pediatrics (G.M., K.T.B., S.K.N.), Department of Medicine, Division of Nephrology and Hypertension, (S.K.N.), and Department of Cellular and Molecular Medicine (S.K.N.), University of California, San Diego, La Jolla, California.
Department of Pediatrics (G.M., K.T.B., S.K.N.), Department of Medicine, Division of Nephrology and Hypertension, (S.K.N.), and Department of Cellular and Molecular Medicine (S.K.N.), University of California, San Diego, La Jolla, California
Drug Metab Dispos. 2016 Jul;44(7):1050-60. doi: 10.1124/dmd.115.068254. Epub 2016 Apr 4.
The hepatocyte nuclear factors, Hnf1a and Hnf4a, in addition to playing key roles in determining hepatocyte fate, have been implicated as candidate lineage-determining transcription factors in the kidney proximal tubule (PT) [Martovetsky et. al., (2012) Mol Pharmacol 84:808], implying an additional level of regulation that is potentially important in developmental and/or tissue-engineering contexts. Mouse embryonic fibroblasts (MEFs) transduced with Hnf1a and Hnf4a form tight junctions and express multiple PT drug transporters (e.g., Slc22a6/Oat1, Slc47a1/Mate1, Slc22a12/Urat1, Abcg2/Bcrp, Abcc2/Mrp2, Abcc4/Mrp4), nutrient transporters (e.g., Slc34a1/NaPi-2, Slco1a6), and tight junction proteins (occludin, claudin 6, ZO-1/Tjp1, ZO-2/Tjp2). In contrast, the coexpression (with Hnf1a and Hnf4a) of GATA binding protein 4 (Gata4), as well as the forkhead box transcription factors, Foxa2 and Foxa3, in MEFs not only downregulates PT markers but also leads to upregulation of several hepatocyte markers, including albumin, apolipoprotein, and transferrin. A similar result was obtained with primary mouse PT cells. Thus, the presence of Gata4 and Foxa2/Foxa3 appears to alter the effect of Hnf1a and Hnf4a by an as-yet unidentified mechanism, leading toward the generation of more hepatocyte-like cells as opposed to cells exhibiting PT characteristics. The different roles of Hnf4a in the kidney and liver was further supported by reanalysis of ChIP-seq data, which revealed Hnf4a colocalization in the kidney near PT-enriched genes compared with those genes enriched in the liver. These findings provide valuable insight, not only into the developmental, and perhaps organotypic, regulation of drug transporters, drug-metabolizing enzymes, and tight junctions, but also for regenerative medicine strategies aimed at restoring the function of the liver and/or kidney (acute kidney injury, AKI; chronic kidney disease, CKD).
肝细胞核因子Hnf1a和Hnf4a,除了在决定肝细胞命运中发挥关键作用外,还被认为是肾近端小管(PT)中候选的谱系决定转录因子[Martovetsky等人,(2012年)《分子药理学》84:808],这意味着在发育和/或组织工程背景下可能存在一个潜在重要的额外调控水平。用Hnf1a和Hnf4a转导的小鼠胚胎成纤维细胞(MEF)形成紧密连接,并表达多种PT药物转运蛋白(如Slc22a6/Oat1、Slc47a1/Mate1、Slc22a12/Urat1、Abcg2/Bcrp、Abcc2/Mrp2、Abcc4/Mrp4)、营养转运蛋白(如Slc34a1/NaPi-2、Slco1a6)和紧密连接蛋白(闭合蛋白、claudin 6、ZO-1/Tjp1、ZO-2/Tjp2)。相比之下,MEF中GATA结合蛋白4(Gata4)以及叉头框转录因子Foxa2和Foxa3与Hnf1a和Hnf4a共表达,不仅会下调PT标志物,还会导致几种肝细胞标志物上调,包括白蛋白、载脂蛋白和转铁蛋白。原代小鼠PT细胞也得到了类似的结果。因此,Gata4和Foxa2/Foxa3的存在似乎通过一种尚未明确的机制改变了Hnf1a和Hnf4a的作用,导致产生更多类似肝细胞的细胞,而不是表现出PT特征的细胞。对ChIP-seq数据的重新分析进一步支持了Hnf4a在肾脏和肝脏中的不同作用,该分析显示与肝脏中富集的基因相比,Hnf4a在肾脏中与PT富集基因共定位。这些发现不仅为药物转运蛋白、药物代谢酶和紧密连接的发育调控以及可能的器官型调控提供了有价值的见解,也为旨在恢复肝脏和/或肾脏功能(急性肾损伤,AKI;慢性肾病,CKD)的再生医学策略提供了有价值的见解。