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Long non-coding RNA GRASLND enhances chondrogenesis via suppression of the interferon type II signaling pathway
The roles of long noncoding RNAs (lncRNAs) in musculoskeletal development, disease, and regeneration remain poorly understood. Here, we identified the novel lncRNA GRASLND (originally named RNF144A-AS1) as a regulator of mesenchymal stem cell (MSC) chondrogenesis. GRASLND, a primate-specific lncRNA,...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7202894/ https://www.ncbi.nlm.nih.gov/pubmed/32202492 http://dx.doi.org/10.7554/eLife.49558 |
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author | Huynh, Nguyen PT Gloss, Catherine C Lorentz, Jeremiah Tang, Ruhang Brunger, Jonathan M McAlinden, Audrey Zhang, Bo Guilak, Farshid |
author_facet | Huynh, Nguyen PT Gloss, Catherine C Lorentz, Jeremiah Tang, Ruhang Brunger, Jonathan M McAlinden, Audrey Zhang, Bo Guilak, Farshid |
author_sort | Huynh, Nguyen PT |
collection | PubMed |
description | The roles of long noncoding RNAs (lncRNAs) in musculoskeletal development, disease, and regeneration remain poorly understood. Here, we identified the novel lncRNA GRASLND (originally named RNF144A-AS1) as a regulator of mesenchymal stem cell (MSC) chondrogenesis. GRASLND, a primate-specific lncRNA, is upregulated during MSC chondrogenesis and appears to act directly downstream of SOX9, but not TGF-β3. We showed that the silencing of GRASLND resulted in lower accumulation of cartilage-like extracellular matrix in a pellet assay, while GRASLND overexpression – either via transgene ectopic expression or by endogenous activation via CRISPR-dCas9-VP64 – significantly enhanced cartilage matrix production. GRASLND acts to inhibit IFN-γ by binding to EIF2AK2, and we further demonstrated that GRASLND exhibits a protective effect in engineered cartilage against interferon type II. Our results indicate an important role of GRASLND in regulating stem cell chondrogenesis, as well as its therapeutic potential in the treatment of cartilage-related diseases, such as osteoarthritis. |
format | Online Article Text |
id | pubmed-7202894 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-72028942020-05-08 Long non-coding RNA GRASLND enhances chondrogenesis via suppression of the interferon type II signaling pathway Huynh, Nguyen PT Gloss, Catherine C Lorentz, Jeremiah Tang, Ruhang Brunger, Jonathan M McAlinden, Audrey Zhang, Bo Guilak, Farshid eLife Stem Cells and Regenerative Medicine The roles of long noncoding RNAs (lncRNAs) in musculoskeletal development, disease, and regeneration remain poorly understood. Here, we identified the novel lncRNA GRASLND (originally named RNF144A-AS1) as a regulator of mesenchymal stem cell (MSC) chondrogenesis. GRASLND, a primate-specific lncRNA, is upregulated during MSC chondrogenesis and appears to act directly downstream of SOX9, but not TGF-β3. We showed that the silencing of GRASLND resulted in lower accumulation of cartilage-like extracellular matrix in a pellet assay, while GRASLND overexpression – either via transgene ectopic expression or by endogenous activation via CRISPR-dCas9-VP64 – significantly enhanced cartilage matrix production. GRASLND acts to inhibit IFN-γ by binding to EIF2AK2, and we further demonstrated that GRASLND exhibits a protective effect in engineered cartilage against interferon type II. Our results indicate an important role of GRASLND in regulating stem cell chondrogenesis, as well as its therapeutic potential in the treatment of cartilage-related diseases, such as osteoarthritis. eLife Sciences Publications, Ltd 2020-03-23 /pmc/articles/PMC7202894/ /pubmed/32202492 http://dx.doi.org/10.7554/eLife.49558 Text en © 2020, Huynh et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Stem Cells and Regenerative Medicine Huynh, Nguyen PT Gloss, Catherine C Lorentz, Jeremiah Tang, Ruhang Brunger, Jonathan M McAlinden, Audrey Zhang, Bo Guilak, Farshid Long non-coding RNA GRASLND enhances chondrogenesis via suppression of the interferon type II signaling pathway |
title | Long non-coding RNA GRASLND enhances chondrogenesis via suppression of the interferon type II signaling pathway |
title_full | Long non-coding RNA GRASLND enhances chondrogenesis via suppression of the interferon type II signaling pathway |
title_fullStr | Long non-coding RNA GRASLND enhances chondrogenesis via suppression of the interferon type II signaling pathway |
title_full_unstemmed | Long non-coding RNA GRASLND enhances chondrogenesis via suppression of the interferon type II signaling pathway |
title_short | Long non-coding RNA GRASLND enhances chondrogenesis via suppression of the interferon type II signaling pathway |
title_sort | long non-coding rna graslnd enhances chondrogenesis via suppression of the interferon type ii signaling pathway |
topic | Stem Cells and Regenerative Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7202894/ https://www.ncbi.nlm.nih.gov/pubmed/32202492 http://dx.doi.org/10.7554/eLife.49558 |
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