Dopamine neurons implanted into people with Parkinson's disease survive without pathology for 14 years

Postmortem analysis of five subjects with Parkinson's disease 9–14 years after transplantation of fetal midbrain cell suspensions revealed surviving grafts that included dopamine and serotonin neurons without pathology. These findings are important for the understanding of the etiopathogenesis...

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Published inNature medicine Vol. 14; no. 5; pp. 507 - 509
Main Authors Mendez, Ivar, Viñuela, Angel, Astradsson, Arnar, Mukhida, Karim, Hallett, Penelope, Robertson, Harold, Tierney, Travis, Holness, Renn, Dagher, Alain, Trojanowski, John Q, Isacson, Ole
Format Journal Article
LanguageEnglish
Published New York Nature Publishing Group US 01.05.2008
Nature Publishing Group
Subjects
Online AccessGet full text
ISSN1078-8956
1546-170X
1546-170X
DOI10.1038/nm1752

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Abstract Postmortem analysis of five subjects with Parkinson's disease 9–14 years after transplantation of fetal midbrain cell suspensions revealed surviving grafts that included dopamine and serotonin neurons without pathology. These findings are important for the understanding of the etiopathogenesis of midbrain dopamine neuron degeneration and future use of cell replacement therapies.
AbstractList Postmortem analysis of five subjects with Parkinson's disease 9-14 years after transplantation of fetal midbrain cell suspensions revealed surviving grafts that included dopamine and serotonin neurons without pathology. These findings are important for the understanding of the etiopathogenesis of midbrain dopamine neuron degeneration and future use of cell replacement therapies.
Postmortem analysis of five subjects with Parkinson's disease 9-14 years after transplantation of fetal midbrain cell suspensions revealed surviving grafts that included dopamine and serotonin neurons without pathology. These findings are important for the understanding of the etiopathogenesis of midbrain dopamine neuron degeneration and future use of cell replacement therapies. [PUBLICATION ABSTRACT]
Postmortem analysis of five subjects with Parkinson’s disease9–14 years after transplantation of fetal midbrain cell suspensions revealed surviving grafts that included dopamine and serotonin neurons without pathology. These findings are important for the understanding of the etiopathogenesis of midbrain dopamine neuron degeneration and future use of cell replacement therapies.
Postmortem analysis of five subjects with Parkinson's disease 9-14 years after transplantation of fetal midbrain cell suspensions revealed surviving grafts that included dopamine and serotonin neurons without pathology. These findings are important for the understanding of the etiopathogenesis of midbrain dopamine neuron degeneration and future use of cell replacement therapies.Postmortem analysis of five subjects with Parkinson's disease 9-14 years after transplantation of fetal midbrain cell suspensions revealed surviving grafts that included dopamine and serotonin neurons without pathology. These findings are important for the understanding of the etiopathogenesis of midbrain dopamine neuron degeneration and future use of cell replacement therapies.
Audience Academic
Author Tierney, Travis
Mukhida, Karim
Hallett, Penelope
Isacson, Ole
Mendez, Ivar
Astradsson, Arnar
Viñuela, Angel
Dagher, Alain
Robertson, Harold
Trojanowski, John Q
Holness, Renn
AuthorAffiliation 2 Harvard University and McLean Hospital, US National Institute of Neurological Disorders and Stroke (NINDS) Udall Parkinson’s Disease Research Center of Excellence, 115 Mill Street, Belmont, Massachusetts 02478, USA
4 Center for Neurodegenerative Disease Research, Department of Pathology and Laboratory Medicine, Institute on Aging of the University of Pennsylvania, NINDS Udall Parkinson’s Disease Research Center of Excellence, 3600 Spruce Street, Philadelphia, Pennsylvania 19104, USA
1 Dalhousie University and Queen Elizabeth II Health Sciences Centre, Division of Neurosurgery and Departments of Anatomy & Neurobiology and Pharmacology, 1976 Summer Street, Halifax, Nova Scotia B3H 3A7, Canada
3 McGill University and Montreal Neurological Institute, McConnell Brain Imaging Centre, 3801 University Street, Montreal, Quebec H3A 2B4, Canada
AuthorAffiliation_xml – name: 3 McGill University and Montreal Neurological Institute, McConnell Brain Imaging Centre, 3801 University Street, Montreal, Quebec H3A 2B4, Canada
– name: 1 Dalhousie University and Queen Elizabeth II Health Sciences Centre, Division of Neurosurgery and Departments of Anatomy & Neurobiology and Pharmacology, 1976 Summer Street, Halifax, Nova Scotia B3H 3A7, Canada
– name: 2 Harvard University and McLean Hospital, US National Institute of Neurological Disorders and Stroke (NINDS) Udall Parkinson’s Disease Research Center of Excellence, 115 Mill Street, Belmont, Massachusetts 02478, USA
– name: 4 Center for Neurodegenerative Disease Research, Department of Pathology and Laboratory Medicine, Institute on Aging of the University of Pennsylvania, NINDS Udall Parkinson’s Disease Research Center of Excellence, 3600 Spruce Street, Philadelphia, Pennsylvania 19104, USA
Author_xml – sequence: 1
  givenname: Ivar
  surname: Mendez
  fullname: Mendez, Ivar
  organization: Division of Neurosurgery and Departments of Anatomy & Neurobiology and Pharmacology, Dalhousie University and Queen Elizabeth II Health Sciences Centre
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  givenname: Angel
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  fullname: Viñuela, Angel
  organization: Harvard University and McLean Hospital, US National Institute of Neurological Disorders and Stroke (NINDS) Udall Parkinson's Disease Research Center of Excellence
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  givenname: Arnar
  surname: Astradsson
  fullname: Astradsson, Arnar
  organization: Harvard University and McLean Hospital, US National Institute of Neurological Disorders and Stroke (NINDS) Udall Parkinson's Disease Research Center of Excellence
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  surname: Mukhida
  fullname: Mukhida, Karim
  organization: Division of Neurosurgery and Departments of Anatomy & Neurobiology and Pharmacology, Dalhousie University and Queen Elizabeth II Health Sciences Centre
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  surname: Hallett
  fullname: Hallett, Penelope
  organization: Harvard University and McLean Hospital, US National Institute of Neurological Disorders and Stroke (NINDS) Udall Parkinson's Disease Research Center of Excellence
– sequence: 6
  givenname: Harold
  surname: Robertson
  fullname: Robertson, Harold
  organization: Division of Neurosurgery and Departments of Anatomy & Neurobiology and Pharmacology, Dalhousie University and Queen Elizabeth II Health Sciences Centre
– sequence: 7
  givenname: Travis
  surname: Tierney
  fullname: Tierney, Travis
  organization: Harvard University and McLean Hospital, US National Institute of Neurological Disorders and Stroke (NINDS) Udall Parkinson's Disease Research Center of Excellence
– sequence: 8
  givenname: Renn
  surname: Holness
  fullname: Holness, Renn
  organization: Division of Neurosurgery and Departments of Anatomy & Neurobiology and Pharmacology, Dalhousie University and Queen Elizabeth II Health Sciences Centre
– sequence: 9
  givenname: Alain
  surname: Dagher
  fullname: Dagher, Alain
  organization: McGill University and Montreal Neurological Institute, McConnell Brain Imaging Centre
– sequence: 10
  givenname: John Q
  surname: Trojanowski
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  organization: Department of Pathology and Laboratory Medicine, Center for Neurodegenerative Disease Research, Institute on Aging of the University of Pennsylvania, NINDS Udall Parkinson's Disease Research Center of Excellence
– sequence: 11
  givenname: Ole
  surname: Isacson
  fullname: Isacson, Ole
  email: isacson@hms.harvard.edu
  organization: Harvard University and McLean Hospital, US National Institute of Neurological Disorders and Stroke (NINDS) Udall Parkinson's Disease Research Center of Excellence
BackLink https://www.ncbi.nlm.nih.gov/pubmed/18391961$$D View this record in MEDLINE/PubMed
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crossref_primary_10_1074_jbc_R113_509588
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crossref_primary_10_3390_s24020575
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crossref_primary_10_1038_mp_2016_121
crossref_primary_10_3389_fnagi_2014_00169
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10.1002/ana.10720
10.1093/jnen/62.12.1241
10.1002/ana.10482
10.1093/brain/awh510
10.1073/pnas.0404700101
10.1056/NEJM200103083441002
10.1038/nm1495
10.1093/brain/awm082
10.1006/exnr.2000.7615
10.1634/stemcells.2006-0744
10.1046/j.1440-1789.2001.00403.x
10.1523/JNEUROSCI.2079-07.2007
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AUTHOR CONTRIBUTIONS
These authors contributed equally to this work.
I.M. and A.V. designed research, performed research, analyzed data and wrote the paper. A.A. and P.H. performed research, analyzed data and wrote the paper. K.M. analyzed data and wrote the paper. H.R., T.T., R.H. and A.D. performed research and analyzed data. J.Q.T. performed neuropathology staining, analyzed raw data, evaluated and interpreted data and wrote the paper. O.I. designed research, performed research, analyzed raw data, evaluated and interpreted data and wrote the paper.
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Snippet Postmortem analysis of five subjects with Parkinson's disease 9–14 years after transplantation of fetal midbrain cell suspensions revealed surviving grafts...
Postmortem analysis of five subjects with Parkinson's disease 9-14 years after transplantation of fetal midbrain cell suspensions revealed surviving grafts...
Postmortem analysis of five subjects with Parkinson’s disease9–14 years after transplantation of fetal midbrain cell suspensions revealed surviving grafts that...
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SubjectTerms Biomedical and Life Sciences
Biomedicine
Brain Tissue Transplantation - methods
Brain Tissue Transplantation - pathology
brief-communication
Cancer Research
Clinical outcomes
Dopamine
Fetal Tissue Transplantation - methods
Fetal Tissue Transplantation - pathology
Humans
Immunohistochemistry
Infectious Diseases
Male
Metabolic Diseases
Middle Aged
Molecular Medicine
Neurons
Neurons - pathology
Neurophysiology
Neurosciences
Neurotransmitters
Parkinson Disease - diagnostic imaging
Parkinson Disease - therapy
Parkinson's disease
Pathology
Phenols
Positron-Emission Tomography
Skin & tissue grafts
Treatment Outcome
Tyrosine 3-Monooxygenase
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Title Dopamine neurons implanted into people with Parkinson's disease survive without pathology for 14 years
URI https://link.springer.com/article/10.1038/nm1752
https://www.ncbi.nlm.nih.gov/pubmed/18391961
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