6533b833fe1ef96bd129c339

RESEARCH PRODUCT

Improved Models of Human Endometrial Organoids Based on Hydrogels from Decellularized Endometrium

Lucía De Miguel-gómezIrene CervellóSara López-martínezEmilio Francés-herreroHannes CampoHortensia FerreroElena Juárez-barberAntonio PellicerAmparo Faus

subject

0301 basic medicineproliferationMedicine (miscellaneous)EndometriumArticleExtracellular matrix03 medical and health sciences0302 clinical medicineIn vivomedicineOrganoidendometriumorganoids030219 obstetrics & reproductive medicineDecellularizationChemistryECM hydrogelRCell biology030104 developmental biologymedicine.anatomical_structureSelf-healing hydrogelsImmunohistochemistryMedicinedecellularizationPancreas

description

Organoids are three-dimensional (3D) multicellular tissue models that mimic their corresponding in vivo tissue. Successful efforts have derived organoids from primary tissues such as intestine, liver, and pancreas. For human uterine endometrium, the recent generation of 3D structures from primary endometrial cells is inspiring new studies of this important tissue using precise preclinical models. To improve on these 3D models, we decellularized pig endometrium containing tissue-specific extracellular matrix and generated a hydrogel (EndoECM). Next, we derived three lines of human endometrial organoids and cultured them in optimal and suboptimal culture expansion media with or without EndoECM (0.01 mg/mL) as a soluble additive. We characterized the resultant organoids to verify their epithelial origin, long-term chromosomal stability, and stemness properties. Lastly, we determined their proliferation potential under different culture conditions using proliferation rates and immunohistochemical methods. Our results demonstrate the importance of a bioactive environment for the maintenance and proliferation of human endometrial organoids.

10.3390/jpm11060504https://www.mdpi.com/2075-4426/11/6/504