The temporal transcriptomic signature of cartilage formation

Author:

Takács Roland1ORCID,Vágó Judit1ORCID,Póliska Szilárd2ORCID,Pushparaj Peter Natesan34ORCID,Ducza László1ORCID,Kovács Patrik1ORCID,Jin Eun-Jung5ORCID,Barrett-Jolley Richard6ORCID,Zákány Róza1ORCID,Matta Csaba1ORCID

Affiliation:

1. Department of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen , Debrecen , H-4032, Hungary

2. Genomic Medicine and Bioinformatic Core Facility, Department of Biochemistry and Molecular Biology, Faculty of Medicine, University of Debrecen , Debrecen  H-4032, Hungary

3. Center of Excellence in Genomic Medicine Research, Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, King Abdulaziz University , Jeddah 21589, Saudi Arabia

4. Center for Transdisciplinary Research, Department of Pharmacology, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences , Chennai , India

5. Department of Biological Sciences, College of Natural Sciences, Wonkwang University , Iksan , Chunbuk 570-749, South Korea

6. Department of Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences, University of Liverpool , Liverpool  L7 8TX, UK

Abstract

Abstract Chondrogenesis is a multistep process, in which cartilage progenitor cells generate a tissue with distinct structural and functional properties. Although several approaches to cartilage regeneration rely on the differentiation of implanted progenitor cells, the temporal transcriptomic landscape of in vitro chondrogenesis in different models has not been reported. Using RNA sequencing, we examined differences in gene expression patterns during cartilage formation in micromass cultures of embryonic limb bud-derived progenitors. Principal component and trajectory analyses revealed a progressively different and distinct transcriptome during chondrogenesis. Differentially expressed genes (DEGs), based on pairwise comparisons of samples from consecutive days were classified into clusters and analysed. We confirmed the involvement of the top DEGs in chondrogenic differentiation using pathway analysis and identified several chondrogenesis-associated transcription factors and collagen subtypes that were not previously linked to cartilage formation. Transient gene silencing of ATOH8 or EBF1 on day 0 attenuated chondrogenesis by deregulating the expression of key osteochondrogenic marker genes in micromass cultures. These results provide detailed insight into the molecular mechanism of chondrogenesis in primary micromass cultures and present a comprehensive dataset of the temporal transcriptomic landscape of chondrogenesis, which may serve as a platform for new molecular approaches in cartilage tissue engineering.

Funder

Eötvös Loránd Research Network

Young Researcher Excellence Programme

National Research, Development and Innovation Office

EU

European Social Fund

National Research, Development and Innovation Fund

European Cooperation in Science and Technology

University of Debrecen

Ministry of Education in Saudi Arabia

National Research Foundation of Korea

MSIT

Biotechnology and B

BBSRC

Publisher

Oxford University Press (OUP)

Subject

Genetics

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