Stem cell antigen/Ly6a protects against bladder fibrosis in mice

We have defined a population of stem cell antigen (Sca)-1 /CD34 /lin mesenchymal stem cells in the mouse urinary bladder. These cells are reduced after partial bladder outlet obstruction (PO). To test the role of Sca-1 expressed by these cells, we analyzed bladders from Sca-1 knockout (KO) mice in b...

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Veröffentlicht in:American journal of physiology. Renal physiology 2019-12, Vol.317 (6), p.F1503-F1512
Hauptverfasser: Tassone, Nicholas M, Li, Belinda, Patel, Mehul S, Devine, Megan Y, Firmiss, Paula R, Gould, Andrew D, Kochan, Kirsten S, Stubbee, Reid A, Bowen, Diana K, Dettman, Robert W, Gong, Edward M
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Sprache:eng
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Zusammenfassung:We have defined a population of stem cell antigen (Sca)-1 /CD34 /lin mesenchymal stem cells in the mouse urinary bladder. These cells are reduced after partial bladder outlet obstruction (PO). To test the role of Sca-1 expressed by these cells, we analyzed bladders from Sca-1 knockout (KO) mice in both uninjured male mice and male mice subjected to PO. We found that loss of Sca-1 alone had little effect on bladder development or function but reduced the total number of mesenchymal stem cells by 30%. After PO, bladders from Sca-1-null KO male mice were larger, with more collagen and less muscle, than obstructed wild-type mice. Steady-state levels of caldesmon were significantly reduced and levels of fibroblast-specific protein 1 were significantly increased in Sca-1 KO mice compared with wild-type mice after PO. In investigating the effects of PO on cell proliferation, we found that loss of Sca-1 changed the timing of cell division in CD34 /lin , collagen-producing, and smooth muscle cells. PO in combination with loss of Sca-1 drastically reduced the ability of CD34 /lin cells to form colonies in vitro. Our findings therefore support the hypothesis that Sca-1 protects the bladder from fibrotic remodeling after obstruction, in part by influencing the proliferation of cells responding to the injury.
ISSN:1931-857X
1522-1466
DOI:10.1152/ajprenal.00160.2019