Liver-Directed Human Amniotic Epithelial Cell Transplantation Improves Systemic Disease Phenotype in Hurler Syndrome Mouse Model. (6th June 2017)

• Record Type: Journal Article
• Authors: Rodriguez, Natalie S.; Yanuaria, Lisa; Parducho, Kevin Murphy R.; Garcia, Irving M.; Varghese, Bino A.; Grubbs, Brendan H.; Miki, Toshio
• Is Part Of: Stem cells translational medicine. Volume 6:Number 7(2017)
• Page Start: 1583
• Page End: 1594
• Publication Date: 2017-06-06
• Subjects: Mucopolysaccharidosis I -- Cell transplantation -- Congenital -- Metabolism -- Amnion -- Placenta; Stem cells -- Periodicals; Regenerative medicine -- Periodicals; Periodicals; 616.0277405
• DOI: 10.1002/sctm.16-0449
• Languages: English
• ISSNs: 2157-6564

Abstract

Abstract: Mucopolysaccharidosis type 1 (MPS1) is an inherited lysosomal storage disorder caused by a deficiency in the glycosaminoglycan (GAG)-degrading enzyme α-L-iduronidase (IDUA). In affected patients, the systemic accumulation of GAGs results in skeletal dysplasia, neurological degeneration, multiple organ dysfunction, and early death. Current therapies, including enzyme replacement and bone marrow transplant, improve life expectancy but the benefits to skeletal and neurological phenotypes are limited. In this study, we tested the therapeutic efficacy of liver-directed transplantation of a placental stem cell, which possesses multilineage differentiation potential, low immunogenicity, and high lysosomal enzyme activity. Unfractionated human amniotic epithelial cells (hAECs) were transplanted directly into the liver of immunodeficient Idua knockout mouse neonates. The hAECs engraftment was immunohistochemically confirmed with anti-human mitochondria staining. Enzyme activity assays indicated that hAECs transplantation restored IDUA function in the liver and significantly decreased urinary GAG excretion. Histochemical and micro-computed tomography analyses revealed reduced GAG deposition in the phalanges joints and composition/morphology improvement of cranial and facial bones. Neurological assessment in the hAEC treated mice showed significant improvement of sensorimotor coordination in the hAEC treated mice compared to untreated mice. Results confirm that partial liver cell replacement with placental stem cells can provide long-term (>20 weeks) and systemic restoration of enzyme function, and lead to significant phenotypic improvement in the MPS1 mouse model. This preclinical data indicate that liver-directed placental stem cell transplantation may improve skeletal and neurological phenotypes of MPS1 patients. Abstract : Rodriguez et al. demonstrated therapeutic efficacy of liver-directed placental stem cell transplantation. Human amniotic epithelial cells (hAECs) were injected into the livers of neonatal mucopolysaccharidosis type 1 model mice and compensated for the missing α-L-iduronidase function. The long-term enzyme restoration resulted in significant neurological and phenotypic improvement suggesting that hAEC transplantation possesses tremendous potential to improve patients' quality of life.