| First Author | Park M | Year | 2020 |
| Journal | Mol Ther | Volume | 28 |
| Issue | 8 | Pages | 1818-1832 |
| PubMed ID | 32534604 | Mgi Jnum | J:307717 |
| Mgi Id | MGI:6724416 | Doi | 10.1016/j.ymthe.2020.05.015 |
| Citation | Park M, et al. (2020) Perivascular Stem Cell-Derived Cyclophilin A Improves Uterine Environment with Asherman's Syndrome via HIF1alpha-Dependent Angiogenesis. Mol Ther 28(8):1818-1832 |
| abstractText | Asherman's syndrome (AS) is characterized by intrauterine adhesions or fibrosis resulting from scarring inside the endometrium. AS is associated with infertility, recurrent miscarriage, and placental abnormalities. Although mesenchymal stem cells show therapeutic promise for the treatment of AS, the molecular mechanisms underlying its pathophysiology remain unclear. We ascertained that mice with AS, like human patients with AS, suffer from extensive fibrosis, oligo/amenorrhea, and infertility. Human perivascular stem cells (hPVSCs) from umbilical cords repaired uterine damage in mice with AS, regardless of their delivery routes. In mice with AS, embryo implantation is aberrantly deferred, which leads to intrauterine growth restriction followed by no delivery at term. hPVSC administration significantly improved implantation defects and subsequent poor pregnancy outcomes via hypoxia inducible factor 1alpha (HIF1alpha)-dependent angiogenesis in a dose-dependent manner. Pharmacologic inhibition of HIF1alpha activity hindered hPVSC actions on pregnancy outcomes, whereas stabilization of HIF1alpha activity facilitated such actions. Furthermore, therapeutic effects of hPVSCs were not observed in uterine-specific HIF1alpha-knockout mice with AS. Secretome analyses of hPVSCs identified cyclophilin-A as the major paracrine factor for hPVSC therapy via HIF1alpha-dependent angiogenesis. Collectively, we demonstrate that hPVSCs-derived cyclophilin-A facilitates HIF1alpha-dependent angiogenesis to ameliorate compromised uterine environments in mice with AS, representing the major pathophysiologic features of humans with AS. |
