Transcriptomic analysis of mouse limb tendon cells during development

Author:

Havis Emmanuelle123,Bonnin Marie-Ange123,Olivera-Martinez Isabel12,Nazaret Nicolas4,Ruggiu Mathilde12,Weibel Jennifer5,Durand Charles12,Guerquin Marie-Justine12,Bonod-Bidaud Christelle6,Ruggiero Florence6,Schweitzer Ronen5,Duprez Delphine123

Affiliation:

1. CNRS UMR 7622, IBPS-Developmental Biology Laboratory, Paris F-75005, France

2. Sorbonne Universités, UPMC Univ Paris 06, IBPS-Developmental Biology Laboratory, Paris F-75005, France

3. Inserm U1156, Paris F-75005, France

4. ProfileXpert, SFR Lyon-Est, UMS 3453 CNRS/US7 INSERM, Lyon F-69008, France

5. Research Division, Shriners Hospital for Children, Portland, OR 97239, USA

6. Institut de Génomique Fonctionnelle de Lyon, Université Lyon 1, CNRS UMR5242, Ecole Normale Supérieure de Lyon, Lyon F-69007, France

Abstract

The molecular signals driving tendon development are not fully identified. We have undertaken a transcriptome analysis of mouse limb tendon cells that were isolated at different stages of development based on scleraxis (Scx) expression. Microarray comparisons allowed us to establish a list of genes regulated in tendon cells during mouse limb development. Bioinformatics analysis of the tendon transcriptome showed that the two most strongly modified signalling pathways were TGF-β and MAPK. TGF-β/SMAD2/3 gain- and loss-of-function experiments in mouse limb explants and mesenchymal stem cells showed that TGF-β signalling was sufficient and required via SMAD2/3 to drive mouse mesodermal stem cells towards the tendon lineage ex vivo and in vitro. TGF-β was also sufficient for tendon gene expression in late limb explants during tendon differentiation. FGF does not have a tenogenic effect and the inhibition of the ERK MAPK signalling pathway was sufficient to activate Scx in mouse limb mesodermal progenitors and mesenchymal stem cells.

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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