SOX9 is required for kidney fibrosis and activates NAV3 to drive renal myofibroblast function

Author:

Raza Sayyid12ORCID,Jokl Elliot12ORCID,Pritchett James3,Martin Katherine12ORCID,Su Kim12ORCID,Simpson Kara12ORCID,Birchall Lindsay12,Mullan Aoibheann F.12,Athwal Varinder S.124ORCID,Doherty Daniel T.12ORCID,Zeef Leo5ORCID,Henderson Neil C.6ORCID,Kalra Philip A.7ORCID,Hanley Neil A.124,Piper Hanley Karen12ORCID

Affiliation:

1. Wellcome Centre for Cell-Matrix Research, Faculty of Biology, Medicine and Health and Manchester Academic Health Science Centre, University of Manchester, Oxford Road, Manchester M13 9PT, UK.

2. Division of Diabetes, Endocrinology and Gastroenterology, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Oxford Road, Manchester, UK.

3. School of Healthcare Science, Manchester Metropolitan University, Manchester M1 5GD, UK.

4. Manchester University NHS Foundation Trust, Oxford Road, Manchester M13 9PT, UK.

5. Bioinformatics Core Facility, Faculty of Life Sciences, University of Manchester, Manchester, UK.

6. MRC Centre for Inflammation Research, Queen’s Medical Research Institute, University of Edinburgh, Edinburgh, UK.

7. Salford Royal NHS Foundation Trust, Stott Lane, Salford, UK.

Abstract

Loss of the transcription factor SOX9 reduces experimentally induced kidney fibrosis in mice.

Funder

Wellcome

Medical Research Council

National Institute for Health Research

Kidney Research UK

Kidneys for Life

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Cell Biology,Molecular Biology,Biochemistry

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