Itga8-Cre-mediated deletion of YAP and TAZ impairs bladder contractility with minimal inflammation and chondrogenic differentiation

Author:

Liu Li12ORCID,Arévalo-Martínez Marycarmen1,Rippe Catarina1,Johansson Martin E.34ORCID,Holmberg Johan1,Albinsson Sebastian1,Swärd Karl1ORCID

Affiliation:

1. Vascular Physiology Environment, Department of Experimental Medical Science, Lund University, Lund, Sweden

2. Department of Urology, Qingyuan People’s Hospital, The Sixth Affiliated Hospital of Guangzhou Medical University, Qingyuan, China

3. Department of Laboratory Medicine, Institute of Biomedicine, Sahlgrenska Center for Cancer Research, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden

4. Department of Clinical Pathology, Sahlgrenska University Hospital, Gothenburg, Sweden

Abstract

This study addresses the hypothesis that YAP and TAZ have an overarching role in the transcriptional hierarchy in the smooth muscle of the urinary bladder by controlling myocardin expression. Using smooth muscle-specific and inducible deletion of YAP and TAZ in adult mice, we find that YAP and TAZ control myocardin expression, contractile differentiation, smooth muscle-specific splicing, and bladder contractility. These effects are largely independent of inflammation and chondrogenic differentiation.

Funder

Swedish Research Council

Cradoord foundation

Novo Nordisk Foundation

Sixth Affiliated Hospital of Guangzhou Medical University, Qingyuan People's Hospital

Margarita Salas stipend funded by the Europe Union-Next Generation EU and University of Valladolid

Kungliga Fysiografiska Sällskapet i Lund

Publisher

American Physiological Society

Subject

Cell Biology,Physiology

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