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The role and possible mechanism of the long noncoding RNA LINC01260 in nonalcoholic fatty liver disease

OBJECTIVE: To investigate the differential expression profile of lncRNAs in the nonalcoholic fatty liver disease (NAFLD) model induced by oleic acid (OA) and to further explore the role of LINC01260 (ENST00000255183) in NAFLD, providing theoretical support for the clinical value of lncRNAs in NAFLD....

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Autores principales: Ge, Xiaoxiao, Sun, Tao, Zhang, Yanmei, Li, Yongqing, Gao, Peng, Zhang, Dantong, Zhang, Bingyang, Wang, Peijun, Ma, Wanshan, Lu, Sumei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8753873/
https://www.ncbi.nlm.nih.gov/pubmed/35016686
http://dx.doi.org/10.1186/s12986-021-00634-4
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author Ge, Xiaoxiao
Sun, Tao
Zhang, Yanmei
Li, Yongqing
Gao, Peng
Zhang, Dantong
Zhang, Bingyang
Wang, Peijun
Ma, Wanshan
Lu, Sumei
author_facet Ge, Xiaoxiao
Sun, Tao
Zhang, Yanmei
Li, Yongqing
Gao, Peng
Zhang, Dantong
Zhang, Bingyang
Wang, Peijun
Ma, Wanshan
Lu, Sumei
author_sort Ge, Xiaoxiao
collection PubMed
description OBJECTIVE: To investigate the differential expression profile of lncRNAs in the nonalcoholic fatty liver disease (NAFLD) model induced by oleic acid (OA) and to further explore the role of LINC01260 (ENST00000255183) in NAFLD, providing theoretical support for the clinical value of lncRNAs in NAFLD. METHODS: OA (50 μg/mL) was used to induce steatosis in normal human LO2 hepatocytes for 48 h and was verified by Oil red O staining. Differential expression profiles of lncRNAs were obtained by eukaryotic circular sequencing (RNA/lncRNA/circRNA-seq) techniques. A gain-of-function (GOF) strategy for LINC01260 was adopted, Oil red O staining and semiquantitative analysis were combined to explore whether the GOF of LINC01260 affects LO2 cell steatosis. CeRNA-based bioinformatics analysis of lncRNAs was performed, and the enriched mRNAs were further verified. RXRB siRNAs were applied and verify its role in LINC01260 regulated OA-induced hepatocytes steatosis. RESULTS: Lipid droplets of different sizes were observed in the cells of the OA group. Absorbance in the OA group was significantly increased after isopropanol decolorization (P < 0.05). Compared with those in the control group, there were 648 lncRNAs with differential expression greater than 1 time in the OA group, of which 351 were upregulated and 297 were downregulated. Fluorescence quantitative PCR showed that the expression of LINC01260 in the OA group was downregulated by 0.35 ± 0.07-fold (P < 0.05). The formation of lipid droplets in LO2 cells of the LINC01260 GOF group decreased significantly (P < 0.05). CeRNA analysis indicated that the mRNA levels of RXRB, RNPEPL1, CD82, MADD and KLC2 were changed to different degrees. Overexpression of LINC01260 significantly induced RXRB transcription (P < 0.05) and translation, and RXRB silence attenuated the lipids decrease induced by LINC01260 overexpression. CONCLUSION: The OA-induced NAFLD cell model has a wide range of lncRNA differential expression profiles. LINC01260 participates in the regulation of the lipid droplet formation process of NAFLD, and its overexpression can significantly inhibit the steatosis process of LO2 cells. Mechanistically, LINC01260 may act as a ceRNA to regulate the expression of RXRB, thereby affecting the adipocytokine signaling pathway. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12986-021-00634-4.
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spelling pubmed-87538732022-01-18 The role and possible mechanism of the long noncoding RNA LINC01260 in nonalcoholic fatty liver disease Ge, Xiaoxiao Sun, Tao Zhang, Yanmei Li, Yongqing Gao, Peng Zhang, Dantong Zhang, Bingyang Wang, Peijun Ma, Wanshan Lu, Sumei Nutr Metab (Lond) Research OBJECTIVE: To investigate the differential expression profile of lncRNAs in the nonalcoholic fatty liver disease (NAFLD) model induced by oleic acid (OA) and to further explore the role of LINC01260 (ENST00000255183) in NAFLD, providing theoretical support for the clinical value of lncRNAs in NAFLD. METHODS: OA (50 μg/mL) was used to induce steatosis in normal human LO2 hepatocytes for 48 h and was verified by Oil red O staining. Differential expression profiles of lncRNAs were obtained by eukaryotic circular sequencing (RNA/lncRNA/circRNA-seq) techniques. A gain-of-function (GOF) strategy for LINC01260 was adopted, Oil red O staining and semiquantitative analysis were combined to explore whether the GOF of LINC01260 affects LO2 cell steatosis. CeRNA-based bioinformatics analysis of lncRNAs was performed, and the enriched mRNAs were further verified. RXRB siRNAs were applied and verify its role in LINC01260 regulated OA-induced hepatocytes steatosis. RESULTS: Lipid droplets of different sizes were observed in the cells of the OA group. Absorbance in the OA group was significantly increased after isopropanol decolorization (P < 0.05). Compared with those in the control group, there were 648 lncRNAs with differential expression greater than 1 time in the OA group, of which 351 were upregulated and 297 were downregulated. Fluorescence quantitative PCR showed that the expression of LINC01260 in the OA group was downregulated by 0.35 ± 0.07-fold (P < 0.05). The formation of lipid droplets in LO2 cells of the LINC01260 GOF group decreased significantly (P < 0.05). CeRNA analysis indicated that the mRNA levels of RXRB, RNPEPL1, CD82, MADD and KLC2 were changed to different degrees. Overexpression of LINC01260 significantly induced RXRB transcription (P < 0.05) and translation, and RXRB silence attenuated the lipids decrease induced by LINC01260 overexpression. CONCLUSION: The OA-induced NAFLD cell model has a wide range of lncRNA differential expression profiles. LINC01260 participates in the regulation of the lipid droplet formation process of NAFLD, and its overexpression can significantly inhibit the steatosis process of LO2 cells. Mechanistically, LINC01260 may act as a ceRNA to regulate the expression of RXRB, thereby affecting the adipocytokine signaling pathway. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12986-021-00634-4. BioMed Central 2022-01-12 /pmc/articles/PMC8753873/ /pubmed/35016686 http://dx.doi.org/10.1186/s12986-021-00634-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ge, Xiaoxiao
Sun, Tao
Zhang, Yanmei
Li, Yongqing
Gao, Peng
Zhang, Dantong
Zhang, Bingyang
Wang, Peijun
Ma, Wanshan
Lu, Sumei
The role and possible mechanism of the long noncoding RNA LINC01260 in nonalcoholic fatty liver disease
title The role and possible mechanism of the long noncoding RNA LINC01260 in nonalcoholic fatty liver disease
title_full The role and possible mechanism of the long noncoding RNA LINC01260 in nonalcoholic fatty liver disease
title_fullStr The role and possible mechanism of the long noncoding RNA LINC01260 in nonalcoholic fatty liver disease
title_full_unstemmed The role and possible mechanism of the long noncoding RNA LINC01260 in nonalcoholic fatty liver disease
title_short The role and possible mechanism of the long noncoding RNA LINC01260 in nonalcoholic fatty liver disease
title_sort role and possible mechanism of the long noncoding rna linc01260 in nonalcoholic fatty liver disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8753873/
https://www.ncbi.nlm.nih.gov/pubmed/35016686
http://dx.doi.org/10.1186/s12986-021-00634-4
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