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Neural progenitor cells from an adult patient with fragile X syndrome.


ABSTRACT: Currently, there is no adequate animal model to study the detailed molecular biochemistry of fragile X syndrome, the leading heritable form of mental impairment. In this study, we sought to establish the use of immature neural cells derived from adult tissues as a novel model of fragile X syndrome that could be used to more fully understand the pathology of this neurogenetic disease.By modifying published methods for the harvest of neural progenitor cells from the post-mortem human brain, neural cells were successfully harvested and grown from post-mortem brain tissue of a 25-year-old adult male with fragile X syndrome, and from brain tissue of a patient with no neurological disease.The cultured fragile X cells displayed many of the characteristics of neural progenitor cells, including nestin and CD133 expression, as well as the biochemical hallmarks of fragile X syndrome, including CGG repeat expansion and a lack of FMRP expression.The successful production of neural cells from an individual with fragile X syndrome opens a new avenue for the scientific study of the molecular basis of this disorder, as well as an approach for studying the efficacy of new therapeutic agents.

SUBMITTER: Schwartz PH 

PROVIDER: S-EPMC545950 | biostudies-literature | 2005 Jan

REPOSITORIES: biostudies-literature

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Neural progenitor cells from an adult patient with fragile X syndrome.

Schwartz Philip H PH   Tassone Flora F   Greco Claudia M CM   Nethercott Hubert E HE   Ziaeian Boback B   Hagerman Randi J RJ   Hagerman Paul J PJ  

BMC medical genetics 20050114


<h4>Background</h4>Currently, there is no adequate animal model to study the detailed molecular biochemistry of fragile X syndrome, the leading heritable form of mental impairment. In this study, we sought to establish the use of immature neural cells derived from adult tissues as a novel model of fragile X syndrome that could be used to more fully understand the pathology of this neurogenetic disease.<h4>Methods</h4>By modifying published methods for the harvest of neural progenitor cells from  ...[more]

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