Masyuk Tatyana, Masyuk Anatoliy, Trussoni Christy, Howard Brynn, Ding Jingyi, Huang Bing, LaRusso Nicholas
Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
JHEP Rep. 2021 Aug 5;3(5):100345. doi: 10.1016/j.jhepr.2021.100345. eCollection 2021 Oct.
BACKGROUND & AIMS: Polycystic liver disease (PLD) is characterised by increased autophagy and reduced miRNA levels in cholangiocytes. Given that autophagy has been implicated in miRNA regulation, we tested the hypothesis that increased autophagy accounts for miRNA reduction in PLD cholangiocytes (PLDCs) and accelerated hepatic cystogenesis.
We assessed miRNA levels in cultured normal human cholangiocytes (NHCs), PLDCs, and isolated PLDC autophagosomes by miRNA-sequencing (miRNA-seq), and miRNA targets by mRNA-seq. Levels of miR-345 and miR-345-targeted proteins in livers of animals and humans with PLD, in NHCs and PLDCs, and in PLDCs transfected with pre-miR-345 were assessed by hybridisation (ISH), quantitative PCR, western blotting, and fluorescence confocal microscopy. We also assessed cell proliferation and cyst growth , and hepatic cystogenesis .
In total, 81% of miRNAs were decreased in PLDCs, with levels of 10 miRNAs reduced by more than 10 times; miR-345 was the most-reduced miRNA. analysis and luciferase reporter assays showed that miR-345 targets included cell-cycle and cell-proliferation-related genes [ cell division cycle 25A (), cyclin-dependent kinase 6 (), , and proliferating cell nuclear antigen ()]; levels of 4 studied miR-345 targets were increased in PLDCs at both the mRNA and protein levels. Transfection of PLDCs with pre-miR-345 increased miR-345 and decreased the expression of miR-345-targeted proteins, cell proliferation, and cyst growth . MiR-345 accumulated in autophagosomes in PLDCs but not NHCs. Inhibition of autophagy increased miR-345 levels, decreased the expression of miR-345-targeted proteins, and reduced hepatic cystogenesis and .
Autophagy-mediated reduction of miR-345 in PLDCs ( miRNAutophagy) accelerates hepatic cystogenesis. Inhibition of autophagy restores miR-345 levels, decreases cyst growth, and is beneficial for PLD.
Polycystic liver disease (PLD) is an incurable genetic disorder characterised by the progressive growth of hepatic cysts. We found that hepatic cystogenesis is increased when the levels of miR-345 in PLD cholangiocytes (PLDCs) are reduced by autophagy. Restoration of miR-345 in PLDCs via inhibition of autophagy decreases hepatic cystogenesis and thus, is beneficial for PLD.
多囊性肝病(PLD)的特征是胆管细胞自噬增加和微小RNA(miRNA)水平降低。鉴于自噬与miRNA调节有关,我们检验了以下假设:自噬增加导致PLD胆管细胞(PLDCs)中miRNA减少,并加速肝囊肿形成。
我们通过miRNA测序(miRNA-seq)评估培养的正常人胆管细胞(NHCs)、PLDCs和分离的PLDC自噬体中的miRNA水平,并通过mRNA测序评估miRNA靶标。通过杂交(ISH)、定量PCR、蛋白质免疫印迹和荧光共聚焦显微镜评估PLD动物和人类肝脏、NHCs和PLDCs以及用pre-miR-345转染的PLDCs中miR-345和miR-345靶向蛋白的水平。我们还评估了细胞增殖和囊肿生长以及肝囊肿形成。
总体而言,PLDCs中81%的miRNA减少,10种miRNA的水平降低了10倍以上;miR-345是减少最多的miRNA。分析和荧光素酶报告基因检测表明,miR-345靶标包括细胞周期和细胞增殖相关基因[细胞分裂周期25A()、细胞周期蛋白依赖性激酶6()、和增殖细胞核抗原()];在PLDCs中,4种研究的miR-345靶标的mRNA和蛋白质水平均升高。用pre-miR-345转染PLDCs可增加miR-345并降低miR-345靶向蛋白的表达、细胞增殖和囊肿生长。miR-345在PLDCs的自噬体中积累,但在NHCs中不积累。抑制自噬可增加miR-345水平,降低miR-345靶向蛋白的表达,并减少肝囊肿形成和。
自噬介导的PLDCs中miR-345减少(miRNA自噬)加速肝囊肿形成。抑制自噬可恢复miR-345水平,减少囊肿生长,对PLD有益。
多囊性肝病(PLD)是一种无法治愈的遗传性疾病,其特征是肝囊肿逐渐生长。我们发现,当自噬使PLD胆管细胞(PLDCs)中的miR-345水平降低时,肝囊肿形成增加。通过抑制自噬恢复PLDCs中的miR-345可减少肝囊肿形成,因此对PLD有益。