Stem Cell Grafting Improves Both Motor and Cognitive Impairments in a Genetic Model of Parkinson's Disease, the Aphakia () Mouse

Stem cell-based cell replacement of lost midbrain dopamine (mDA) neurons is a potential therapy for Parkinson's disease (PD). Toward this goal, it is critical to optimize various aspects of cell transplantation and to assess functional recovery through behavioral tests in validated animal model...

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Main Authors: Jisook Moon Ph.D., Hyun-Seob Lee, Jun Mo Kang, Junpil Park, Amanda Leung, Sunghoi Hong, Sangmi Chung, Kwang-Soo Kim Ph.D.
Format: Article
Language:English
Published: SAGE Publishing 2013-07-01
Series:Cell Transplantation
Online Access:https://doi.org/10.3727/096368912X657242
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spelling doaj-e6003da085e44c0eb9dc892bb95300ef2020-11-25T03:46:27ZengSAGE PublishingCell Transplantation0963-68971555-38922013-07-012210.3727/096368912X657242Stem Cell Grafting Improves Both Motor and Cognitive Impairments in a Genetic Model of Parkinson's Disease, the Aphakia () MouseJisook Moon Ph.D.0Hyun-Seob Lee1Jun Mo Kang2Junpil Park3Amanda Leung4Sunghoi Hong5Sangmi Chung6Kwang-Soo Kim Ph.D.7Department of Bioengineering, College of Life Science, CHA University, Seoul, KoreaDepartment of Bioengineering, College of Life Science, CHA University, Seoul, KoreaDepartment of Bioengineering, College of Life Science, CHA University, Seoul, KoreaMolecular Neurobiology Laboratory, McLean Hospital/Harvard Medical School, Belmont, MA, USAMolecular Neurobiology Laboratory, McLean Hospital/Harvard Medical School, Belmont, MA, USAMolecular Neurobiology Laboratory, McLean Hospital/Harvard Medical School, Belmont, MA, USAMolecular Neurobiology Laboratory, McLean Hospital/Harvard Medical School, Belmont, MA, USAMolecular Neurobiology Laboratory, McLean Hospital/Harvard Medical School, Belmont, MA, USAStem cell-based cell replacement of lost midbrain dopamine (mDA) neurons is a potential therapy for Parkinson's disease (PD). Toward this goal, it is critical to optimize various aspects of cell transplantation and to assess functional recovery through behavioral tests in validated animal model(s) of PD. At present, cell transplantation studies are being done almost exclusively in neurotoxin-based animal models, because few genetic models of PD exhibit robust mDA neuronal loss. Here we used a genetic model of PD, the aphakia mouse, which demonstrates selective degeneration of mDA neurons in the substantia nigra. We systematically investigated the functional effects of transplanting embryonic stem cell-derived cells at different stages of in vitro differentiation: embryoid body (EB), neural progenitor (NP), and neuronal differentiated (ND) stages. We found that transplantation of NP cells yielded the best outcomes for both survival and behavioral improvement, while transplantation of EB and ND cells resulted in high teratoma-like tumor formation and poor survival, respectively. In behavioral paradigms specific to basal ganglia, the NP cells group prominently improved motor behavioral defects 1 and 2 months posttransplantation. Furthermore, we found that NP cell transplantation also improved cognitive impairments of aphakia mice, as examined by the passive avoidance task. Importantly, these graft-induced functional improvements well correlated with survival of tyrosine hydroxylase-positive DA neurons. Taken together, we propose that the aphakia mouse can serve as a novel and useful platform for cell transplantation studies to assess both neurological and cognitive improvements and that NP stage cells represent an optimal stage for transplantation.https://doi.org/10.3727/096368912X657242
collection DOAJ
language English
format Article
sources DOAJ
author Jisook Moon Ph.D.
Hyun-Seob Lee
Jun Mo Kang
Junpil Park
Amanda Leung
Sunghoi Hong
Sangmi Chung
Kwang-Soo Kim Ph.D.
spellingShingle Jisook Moon Ph.D.
Hyun-Seob Lee
Jun Mo Kang
Junpil Park
Amanda Leung
Sunghoi Hong
Sangmi Chung
Kwang-Soo Kim Ph.D.
Stem Cell Grafting Improves Both Motor and Cognitive Impairments in a Genetic Model of Parkinson's Disease, the Aphakia () Mouse
Cell Transplantation
author_facet Jisook Moon Ph.D.
Hyun-Seob Lee
Jun Mo Kang
Junpil Park
Amanda Leung
Sunghoi Hong
Sangmi Chung
Kwang-Soo Kim Ph.D.
author_sort Jisook Moon Ph.D.
title Stem Cell Grafting Improves Both Motor and Cognitive Impairments in a Genetic Model of Parkinson's Disease, the Aphakia () Mouse
title_short Stem Cell Grafting Improves Both Motor and Cognitive Impairments in a Genetic Model of Parkinson's Disease, the Aphakia () Mouse
title_full Stem Cell Grafting Improves Both Motor and Cognitive Impairments in a Genetic Model of Parkinson's Disease, the Aphakia () Mouse
title_fullStr Stem Cell Grafting Improves Both Motor and Cognitive Impairments in a Genetic Model of Parkinson's Disease, the Aphakia () Mouse
title_full_unstemmed Stem Cell Grafting Improves Both Motor and Cognitive Impairments in a Genetic Model of Parkinson's Disease, the Aphakia () Mouse
title_sort stem cell grafting improves both motor and cognitive impairments in a genetic model of parkinson's disease, the aphakia () mouse
publisher SAGE Publishing
series Cell Transplantation
issn 0963-6897
1555-3892
publishDate 2013-07-01
description Stem cell-based cell replacement of lost midbrain dopamine (mDA) neurons is a potential therapy for Parkinson's disease (PD). Toward this goal, it is critical to optimize various aspects of cell transplantation and to assess functional recovery through behavioral tests in validated animal model(s) of PD. At present, cell transplantation studies are being done almost exclusively in neurotoxin-based animal models, because few genetic models of PD exhibit robust mDA neuronal loss. Here we used a genetic model of PD, the aphakia mouse, which demonstrates selective degeneration of mDA neurons in the substantia nigra. We systematically investigated the functional effects of transplanting embryonic stem cell-derived cells at different stages of in vitro differentiation: embryoid body (EB), neural progenitor (NP), and neuronal differentiated (ND) stages. We found that transplantation of NP cells yielded the best outcomes for both survival and behavioral improvement, while transplantation of EB and ND cells resulted in high teratoma-like tumor formation and poor survival, respectively. In behavioral paradigms specific to basal ganglia, the NP cells group prominently improved motor behavioral defects 1 and 2 months posttransplantation. Furthermore, we found that NP cell transplantation also improved cognitive impairments of aphakia mice, as examined by the passive avoidance task. Importantly, these graft-induced functional improvements well correlated with survival of tyrosine hydroxylase-positive DA neurons. Taken together, we propose that the aphakia mouse can serve as a novel and useful platform for cell transplantation studies to assess both neurological and cognitive improvements and that NP stage cells represent an optimal stage for transplantation.
url https://doi.org/10.3727/096368912X657242
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