Cargando…

NFAT1 protects articular cartilage against osteoarthritic degradation by directly regulating transcription of specific anabolic and catabolic genes

OBJECTIVES: Adult mice lacking the transcription factor NFAT1 exhibit osteoarthritis (OA). The precise molecular mechanism for NFAT1 deficiency-induced osteoarthritic cartilage degradation remains to be clarified. This study aimed to investigate if NFAT1 protects articular cartilage (AC) against OA...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, M., Lu, Q., Budden, T., Wang, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6397328/
https://www.ncbi.nlm.nih.gov/pubmed/30915215
http://dx.doi.org/10.1302/2046-3758.82.BJR-2018-0114.R1
_version_ 1783399409657053184
author Zhang, M.
Lu, Q.
Budden, T.
Wang, J.
author_facet Zhang, M.
Lu, Q.
Budden, T.
Wang, J.
author_sort Zhang, M.
collection PubMed
description OBJECTIVES: Adult mice lacking the transcription factor NFAT1 exhibit osteoarthritis (OA). The precise molecular mechanism for NFAT1 deficiency-induced osteoarthritic cartilage degradation remains to be clarified. This study aimed to investigate if NFAT1 protects articular cartilage (AC) against OA by directly regulating the transcription of specific catabolic and anabolic genes in articular chondrocytes. METHODS: Through a combined approach of gene expression analysis and web-based searching of NFAT1 binding sequences, 25 candidate target genes that displayed aberrant expression in Nfat1(-/-) AC at the initiation stage of OA, and possessed at least four NFAT1 binding sites in the promoter of each gene, were selected and tested for NFAT1 transcriptional activities by chromatin immunoprecipitation (ChIP) and promoter luciferase reporter assays using chondrocytes isolated from the AC of three- to four-month-old wild-type mice or Nfat1(-/-) mice with early OA phenotype. RESULTS: Chromatin immunoprecipitation assays revealed that NFAT1 bound directly to the promoter of 21 of the 25 tested genes encoding cartilage-matrix proteins, growth factors, inflammatory cytokines, matrix-degrading proteinases, and specific transcription factors. Promoter luciferase reporter assays of representative anabolic and catabolic genes demonstrated that NFAT1-DNA binding functionally regulated the luciferase activity of specific target genes in wild-type chondrocytes, but not in Nfat1(-/-) chondrocytes or in wild-type chondrocytes transfected with plasmids containing mutated NFAT1 binding sequences. CONCLUSION: NFAT1 protects AC against degradation by directly regulating the transcription of target genes in articular chondrocytes. NFAT1 deficiency causes defective transcription of specific anabolic and catabolic genes in articular chondrocytes, leading to increased matrix catabolism and osteoarthritic cartilage degradation. Cite this article: M. Zhang, Q. Lu, T. Budden, J. Wang. NFAT1 protects articular cartilage against osteoarthritic degradation by directly regulating transcription of specific anabolic and catabolic genes. Bone Joint Res 2019;8:90–100. DOI: 10.1302/2046-3758.82.BJR-2018-0114.R1.
format Online
Article
Text
id pubmed-6397328
institution National Center for Biotechnology Information
language English
publishDate 2019
record_format MEDLINE/PubMed
spelling pubmed-63973282019-03-26 NFAT1 protects articular cartilage against osteoarthritic degradation by directly regulating transcription of specific anabolic and catabolic genes Zhang, M. Lu, Q. Budden, T. Wang, J. Bone Joint Res Osteoarthritis OBJECTIVES: Adult mice lacking the transcription factor NFAT1 exhibit osteoarthritis (OA). The precise molecular mechanism for NFAT1 deficiency-induced osteoarthritic cartilage degradation remains to be clarified. This study aimed to investigate if NFAT1 protects articular cartilage (AC) against OA by directly regulating the transcription of specific catabolic and anabolic genes in articular chondrocytes. METHODS: Through a combined approach of gene expression analysis and web-based searching of NFAT1 binding sequences, 25 candidate target genes that displayed aberrant expression in Nfat1(-/-) AC at the initiation stage of OA, and possessed at least four NFAT1 binding sites in the promoter of each gene, were selected and tested for NFAT1 transcriptional activities by chromatin immunoprecipitation (ChIP) and promoter luciferase reporter assays using chondrocytes isolated from the AC of three- to four-month-old wild-type mice or Nfat1(-/-) mice with early OA phenotype. RESULTS: Chromatin immunoprecipitation assays revealed that NFAT1 bound directly to the promoter of 21 of the 25 tested genes encoding cartilage-matrix proteins, growth factors, inflammatory cytokines, matrix-degrading proteinases, and specific transcription factors. Promoter luciferase reporter assays of representative anabolic and catabolic genes demonstrated that NFAT1-DNA binding functionally regulated the luciferase activity of specific target genes in wild-type chondrocytes, but not in Nfat1(-/-) chondrocytes or in wild-type chondrocytes transfected with plasmids containing mutated NFAT1 binding sequences. CONCLUSION: NFAT1 protects AC against degradation by directly regulating the transcription of target genes in articular chondrocytes. NFAT1 deficiency causes defective transcription of specific anabolic and catabolic genes in articular chondrocytes, leading to increased matrix catabolism and osteoarthritic cartilage degradation. Cite this article: M. Zhang, Q. Lu, T. Budden, J. Wang. NFAT1 protects articular cartilage against osteoarthritic degradation by directly regulating transcription of specific anabolic and catabolic genes. Bone Joint Res 2019;8:90–100. DOI: 10.1302/2046-3758.82.BJR-2018-0114.R1. 2019-03-02 /pmc/articles/PMC6397328/ /pubmed/30915215 http://dx.doi.org/10.1302/2046-3758.82.BJR-2018-0114.R1 Text en © 2019 Author(s) et al. This is an open-access article distributed under the terms of the Creative Commons Attributions licence (CC-BY-NC), which permits unrestricted use, distribution, and reproduction in any medium, but not for commercial gain, provided the original author and source are credited.
spellingShingle Osteoarthritis
Zhang, M.
Lu, Q.
Budden, T.
Wang, J.
NFAT1 protects articular cartilage against osteoarthritic degradation by directly regulating transcription of specific anabolic and catabolic genes
title NFAT1 protects articular cartilage against osteoarthritic degradation by directly regulating transcription of specific anabolic and catabolic genes
title_full NFAT1 protects articular cartilage against osteoarthritic degradation by directly regulating transcription of specific anabolic and catabolic genes
title_fullStr NFAT1 protects articular cartilage against osteoarthritic degradation by directly regulating transcription of specific anabolic and catabolic genes
title_full_unstemmed NFAT1 protects articular cartilage against osteoarthritic degradation by directly regulating transcription of specific anabolic and catabolic genes
title_short NFAT1 protects articular cartilage against osteoarthritic degradation by directly regulating transcription of specific anabolic and catabolic genes
title_sort nfat1 protects articular cartilage against osteoarthritic degradation by directly regulating transcription of specific anabolic and catabolic genes
topic Osteoarthritis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6397328/
https://www.ncbi.nlm.nih.gov/pubmed/30915215
http://dx.doi.org/10.1302/2046-3758.82.BJR-2018-0114.R1
work_keys_str_mv AT zhangm nfat1protectsarticularcartilageagainstosteoarthriticdegradationbydirectlyregulatingtranscriptionofspecificanabolicandcatabolicgenes
AT luq nfat1protectsarticularcartilageagainstosteoarthriticdegradationbydirectlyregulatingtranscriptionofspecificanabolicandcatabolicgenes
AT buddent nfat1protectsarticularcartilageagainstosteoarthriticdegradationbydirectlyregulatingtranscriptionofspecificanabolicandcatabolicgenes
AT wangj nfat1protectsarticularcartilageagainstosteoarthriticdegradationbydirectlyregulatingtranscriptionofspecificanabolicandcatabolicgenes