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Glial cell line-derived neurotrophic factor-secreting human neural progenitors show long-term survival, maturation into astrocytes, and no tumor formation following transplantation into the spinal cord of immunocompromised rats

Human neural progenitor cells (hNPCs) derived from the fetal cortex can be expanded in vitro and genetically modified through lentiviral transduction to secrete growth factors shown to have a neurotrophic effect in animal models of neurological disease. hNPCs survive and mature following transplanta...

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Autores principales: Gowing, Geneviève, Shelley, Brandon, Staggenborg, Kevin, Hurley, Amanda, Avalos, Pablo, Victoroff, Jesse, Latter, Jessica, Garcia, Leslie, Svendsen, Clive N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3969154/
https://www.ncbi.nlm.nih.gov/pubmed/24284956
http://dx.doi.org/10.1097/WNR.0000000000000092
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author Gowing, Geneviève
Shelley, Brandon
Staggenborg, Kevin
Hurley, Amanda
Avalos, Pablo
Victoroff, Jesse
Latter, Jessica
Garcia, Leslie
Svendsen, Clive N.
author_facet Gowing, Geneviève
Shelley, Brandon
Staggenborg, Kevin
Hurley, Amanda
Avalos, Pablo
Victoroff, Jesse
Latter, Jessica
Garcia, Leslie
Svendsen, Clive N.
author_sort Gowing, Geneviève
collection PubMed
description Human neural progenitor cells (hNPCs) derived from the fetal cortex can be expanded in vitro and genetically modified through lentiviral transduction to secrete growth factors shown to have a neurotrophic effect in animal models of neurological disease. hNPCs survive and mature following transplantation into the central nervous system of large and small animals including the rat model of amyotrophic lateral sclerosis. Here we report that hNPCs engineered to express glial cell line-derived neurotrophic factor (GDNF) survive long-term (7.5 months) following transplantation into the spinal cord of athymic nude rats and continue to secrete GDNF. Cell proliferation declined while the number of astrocytes increased, suggesting final maturation of the cells over time in vivo. Together these data show that GDNF-producing hNPCs may be useful as a source of cells for long-term delivery of both astrocytes and GDNF to the damaged central nervous system.
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spelling pubmed-39691542014-03-31 Glial cell line-derived neurotrophic factor-secreting human neural progenitors show long-term survival, maturation into astrocytes, and no tumor formation following transplantation into the spinal cord of immunocompromised rats Gowing, Geneviève Shelley, Brandon Staggenborg, Kevin Hurley, Amanda Avalos, Pablo Victoroff, Jesse Latter, Jessica Garcia, Leslie Svendsen, Clive N. Neuroreport Engineered Cells Human neural progenitor cells (hNPCs) derived from the fetal cortex can be expanded in vitro and genetically modified through lentiviral transduction to secrete growth factors shown to have a neurotrophic effect in animal models of neurological disease. hNPCs survive and mature following transplantation into the central nervous system of large and small animals including the rat model of amyotrophic lateral sclerosis. Here we report that hNPCs engineered to express glial cell line-derived neurotrophic factor (GDNF) survive long-term (7.5 months) following transplantation into the spinal cord of athymic nude rats and continue to secrete GDNF. Cell proliferation declined while the number of astrocytes increased, suggesting final maturation of the cells over time in vivo. Together these data show that GDNF-producing hNPCs may be useful as a source of cells for long-term delivery of both astrocytes and GDNF to the damaged central nervous system. Lippincott Williams & Wilkins 2014-04-16 2014-04-11 /pmc/articles/PMC3969154/ /pubmed/24284956 http://dx.doi.org/10.1097/WNR.0000000000000092 Text en © 2014 Wolters Kluwer Health | Lippincott Williams & Wilkins http://creativecommons.org/licenses/by-nc-nd/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivitives 3.0 License, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially.
spellingShingle Engineered Cells
Gowing, Geneviève
Shelley, Brandon
Staggenborg, Kevin
Hurley, Amanda
Avalos, Pablo
Victoroff, Jesse
Latter, Jessica
Garcia, Leslie
Svendsen, Clive N.
Glial cell line-derived neurotrophic factor-secreting human neural progenitors show long-term survival, maturation into astrocytes, and no tumor formation following transplantation into the spinal cord of immunocompromised rats
title Glial cell line-derived neurotrophic factor-secreting human neural progenitors show long-term survival, maturation into astrocytes, and no tumor formation following transplantation into the spinal cord of immunocompromised rats
title_full Glial cell line-derived neurotrophic factor-secreting human neural progenitors show long-term survival, maturation into astrocytes, and no tumor formation following transplantation into the spinal cord of immunocompromised rats
title_fullStr Glial cell line-derived neurotrophic factor-secreting human neural progenitors show long-term survival, maturation into astrocytes, and no tumor formation following transplantation into the spinal cord of immunocompromised rats
title_full_unstemmed Glial cell line-derived neurotrophic factor-secreting human neural progenitors show long-term survival, maturation into astrocytes, and no tumor formation following transplantation into the spinal cord of immunocompromised rats
title_short Glial cell line-derived neurotrophic factor-secreting human neural progenitors show long-term survival, maturation into astrocytes, and no tumor formation following transplantation into the spinal cord of immunocompromised rats
title_sort glial cell line-derived neurotrophic factor-secreting human neural progenitors show long-term survival, maturation into astrocytes, and no tumor formation following transplantation into the spinal cord of immunocompromised rats
topic Engineered Cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3969154/
https://www.ncbi.nlm.nih.gov/pubmed/24284956
http://dx.doi.org/10.1097/WNR.0000000000000092
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