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Stem cells act through multiple mechanisms to benefit mice with neurodegenerative metabolic disease.

Stem cells act through multiple mechanisms to benefit mice with neurodegenerative metabolic disease. Research Abstract Details 

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  • Stem cells act through multiple mechanisms to benefit mice with neurodegenerative metabolic disease. Abstract Text:

    jean-pyo leeJean-Pyo Lee,mylvaganam jeyakumarMylvaganam Jeyakumar,rodolfo gonzalezRodolfo Gonzalez,hiroto takahashiHiroto Takahashi,pei-jen leePei-Jen Lee,rena c baekRena C Baek,dan clarkDan Clark,heather roseHeather Rose,gerald fuGerald Fu,jonathan clarkeJonathan Clarke,scott mckercherScott McKercher,jennifer meerlooJennifer Meerloo,franz-josef mullerFranz-Josef Muller,kook in parkKook In Park,terry d buttersTerry D Butters,raymond a dwekRaymond A Dwek,philip schwartzPhilip Schwartz,gang tongGang Tong,david wengerDavid Wenger,stuart a liptonStuart A Lipton,thomas n seyfriedThomas N Seyfried,frances m plattFrances M Platt,evan y snyderEvan Y Snyder,

    Intracranial transplantation of neural stem cells (NSCs) delayed disease onset, preserved motor function, reduced pathology and prolonged survival in a mouse model of Sandhoff disease, a lethal gangliosidosis. Although donor-derived neurons were electrophysiologically active within chimeric regions, the small degree of neuronal replacement alone could not account for the improvement. NSCs also increased brain beta-hexosaminidase levels, reduced ganglioside storage and diminished activated microgliosis. Additionally, when oral glycosphingolipid biosynthesis inhibitors (beta-hexosaminidase substrate inhibitors) were combined with NSC transplantation, substantial synergy resulted. Efficacy extended to human NSCs, both to those isolated directly from the central nervous system (CNS) and to those derived secondarily from embryonic stem cells. Appreciating that NSCs exhibit a broad repertoire of potentially therapeutic actions, of which neuronal replacement is but one, may help in formulating rational multimodal strategies for the treatment of neurodegenerative diseases.

    Stem cells act through multiple mechanisms to benefit mice with neurodegenerative metabolic disease. Publishing Authors By Initials

    jp leeJP Lee,m jeyakumarM Jeyakumar,r gonzalezR Gonzalez,h takahashiH Takahashi,pj leePJ Lee,rc baekRC Baek,d clarkD Clark,h roseH Rose,g fuG Fu,j clarkeJ Clarke,s mckercherS McKercher,j meerlooJ Meerloo,fj mullerFJ Muller,ki parkKI Park,td buttersTD Butters,ra dwekRA Dwek,p schwartzP Schwartz,g tongG Tong,d wengerD Wenger,sa liptonSA Lipton,tn seyfriedTN Seyfried,fm plattFM Platt,ey snyderEY Snyder,

    For similar enzymes and coenzymes: enzymes: hydrolases: glycoside hydrolases: hexosaminidases: beta-n-acetylhexosaminidases research abstracts see: enzymes and coenzymes: enzymes: hydrolases: glycoside hydrolases: hexosaminidases: beta-n-acetylhexosaminidases research

    PUBMED ID PMID:

    MEDLINE DATE:

    Stem cells act through multiple mechanisms to benefit mice with neurodegenerative metabolic disease. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Nature medicine

    VOLUME: 13

    Page Numbers: 439-47

    Journal Abbreviation:

    ISSN: 1078-8956

    DAY: 11

    MONTH: 03

    YEAR: 2007

    Stem cells act through multiple mechanisms to benefit mice with neurodegenerative metabolic disease. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9502015

    Stem cells act through multiple mechanisms to benefit mice with neurodegenerative metabolic disease. Keywords Mesh Terms:

    KEYWORDS: beta-N-Acetylhexosaminidases

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Stem cells act through multiple mechanisms to benefit mice with neurodegenerative metabolic disease. Information

    Substance Name: beta-N-Acetylhexosaminidases

    Registry Number: EC 3.2.1.52

    Grant and Affiliation Information for Stem cells act through multiple mechanisms to benefit mice with neurodegenerative metabolic disease.

    AFFILIATION: Stem Cell & Regeneration Program, Center for Neuroscience and Aging Research, Burnham Institute for Medical Research, La Jolla, California 92037, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Nat Med

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