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Autophagy-mediated reduction of miR-345 contributes to hepatic cystogenesis in polycystic liver disease

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...

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Autores principales: Masyuk, Tatyana, Masyuk, Anatoliy, Trussoni, Christy, Howard, Brynn, Ding, Jingyi, Huang, Bing, LaRusso, Nicholas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8449272/
https://www.ncbi.nlm.nih.gov/pubmed/34568801
http://dx.doi.org/10.1016/j.jhepr.2021.100345
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author Masyuk, Tatyana
Masyuk, Anatoliy
Trussoni, Christy
Howard, Brynn
Ding, Jingyi
Huang, Bing
LaRusso, Nicholas
author_facet Masyuk, Tatyana
Masyuk, Anatoliy
Trussoni, Christy
Howard, Brynn
Ding, Jingyi
Huang, Bing
LaRusso, Nicholas
author_sort Masyuk, Tatyana
collection PubMed
description 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. METHODS: 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 in situ hybridisation (ISH), quantitative PCR, western blotting, and fluorescence confocal microscopy. We also assessed cell proliferation and cyst growth in vitro, and hepatic cystogenesis in vivo. RESULTS: 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. In silico analysis and luciferase reporter assays showed that miR-345 targets included cell-cycle and cell-proliferation-related genes [i.e. cell division cycle 25A (CDC25A), cyclin-dependent kinase 6 (CDK6), E2F2, and proliferating cell nuclear antigen (PCNA)]; 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 in vitro. 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 in vitro and in vivo. CONCLUSION: Autophagy-mediated reduction of miR-345 in PLDCs (i.e. miRNAutophagy) accelerates hepatic cystogenesis. Inhibition of autophagy restores miR-345 levels, decreases cyst growth, and is beneficial for PLD. LAY SUMMARY: 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.
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spelling pubmed-84492722021-09-24 Autophagy-mediated reduction of miR-345 contributes to hepatic cystogenesis in polycystic liver disease Masyuk, Tatyana Masyuk, Anatoliy Trussoni, Christy Howard, Brynn Ding, Jingyi Huang, Bing LaRusso, Nicholas JHEP Rep Research Article 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. METHODS: 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 in situ hybridisation (ISH), quantitative PCR, western blotting, and fluorescence confocal microscopy. We also assessed cell proliferation and cyst growth in vitro, and hepatic cystogenesis in vivo. RESULTS: 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. In silico analysis and luciferase reporter assays showed that miR-345 targets included cell-cycle and cell-proliferation-related genes [i.e. cell division cycle 25A (CDC25A), cyclin-dependent kinase 6 (CDK6), E2F2, and proliferating cell nuclear antigen (PCNA)]; 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 in vitro. 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 in vitro and in vivo. CONCLUSION: Autophagy-mediated reduction of miR-345 in PLDCs (i.e. miRNAutophagy) accelerates hepatic cystogenesis. Inhibition of autophagy restores miR-345 levels, decreases cyst growth, and is beneficial for PLD. LAY SUMMARY: 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. Elsevier 2021-08-05 /pmc/articles/PMC8449272/ /pubmed/34568801 http://dx.doi.org/10.1016/j.jhepr.2021.100345 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Masyuk, Tatyana
Masyuk, Anatoliy
Trussoni, Christy
Howard, Brynn
Ding, Jingyi
Huang, Bing
LaRusso, Nicholas
Autophagy-mediated reduction of miR-345 contributes to hepatic cystogenesis in polycystic liver disease
title Autophagy-mediated reduction of miR-345 contributes to hepatic cystogenesis in polycystic liver disease
title_full Autophagy-mediated reduction of miR-345 contributes to hepatic cystogenesis in polycystic liver disease
title_fullStr Autophagy-mediated reduction of miR-345 contributes to hepatic cystogenesis in polycystic liver disease
title_full_unstemmed Autophagy-mediated reduction of miR-345 contributes to hepatic cystogenesis in polycystic liver disease
title_short Autophagy-mediated reduction of miR-345 contributes to hepatic cystogenesis in polycystic liver disease
title_sort autophagy-mediated reduction of mir-345 contributes to hepatic cystogenesis in polycystic liver disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8449272/
https://www.ncbi.nlm.nih.gov/pubmed/34568801
http://dx.doi.org/10.1016/j.jhepr.2021.100345
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