bioRxiv preprint doi: https://doi.org/10.1101/2020.08.21.257154; this version posted October 20, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Restricted differentiative capacity of Wt1-expressing peritoneal mesothelium in postnatal and adult mice. Thomas P Wilm1, Helen Tanton1,3, Fiona Mutter1, Veronica Foisor1,4, Ben Middlehurst1, Kelly Ward1, Tarek Benameur1,5, Nicholas Hastie2, Bettina Wilm1^ Affiliation: 1 Department of Molecular Physiology and Cell Signalling, Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Liverpool, UK 2 MRC Human Genetics Unit, University of Edinburgh, Edinburgh, UK 3 present address: Department of Oncologic Pathology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, USA 4 present address: Department of Chemistry, University of Warwick, Coventry, UK 5 present address: College of Medicine, Department of Biomedical Sciences, King Faisal University, Al Ahsa, Kingdom of Saudi Arabia ORCIDs: HT 0000-0002-0129-5870 VF 0000-0001-7004-1324 NH 0000-0002-0515-168X BW 0000-0002-9245-993X ^ Corresponding author:
[email protected] bioRxiv preprint doi: https://doi.org/10.1101/2020.08.21.257154; this version posted October 20, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Abstract Previously, genetic lineage tracing based on the mesothelial marker Wt1, appeared to show that peritoneal mesothelial cells have a range of differentiative capacities and are the direct progenitors of vascular smooth muscle in the intestine.