Progenitor cell-based treatment of glial disease

Research output: Chapter in Book/Report/Conference proceedingBook chapterResearchpeer-review

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Progenitor cell-based treatment of glial disease. / Goldman, Steven A.

Functional Neural Transplantation IV. Vol. 231 Cambridge, MA, United States, 2017. p. 165-189 (Progress in Brain Research, Vol. 231).

Research output: Chapter in Book/Report/Conference proceedingBook chapterResearchpeer-review

Harvard

Goldman, SA 2017, Progenitor cell-based treatment of glial disease. in Functional Neural Transplantation IV. vol. 231, Cambridge, MA, United States, Progress in Brain Research, vol. 231, pp. 165-189. https://doi.org/10.1016/bs.pbr.2017.02.010

APA

Goldman, S. A. (2017). Progenitor cell-based treatment of glial disease. In Functional Neural Transplantation IV (Vol. 231, pp. 165-189). Progress in Brain Research Vol. 231 https://doi.org/10.1016/bs.pbr.2017.02.010

Vancouver

Goldman SA. Progenitor cell-based treatment of glial disease. In Functional Neural Transplantation IV. Vol. 231. Cambridge, MA, United States. 2017. p. 165-189. (Progress in Brain Research, Vol. 231). https://doi.org/10.1016/bs.pbr.2017.02.010

Author

Goldman, Steven A. / Progenitor cell-based treatment of glial disease. Functional Neural Transplantation IV. Vol. 231 Cambridge, MA, United States, 2017. pp. 165-189 (Progress in Brain Research, Vol. 231).

Bibtex

@inbook{a2f49047d39e43b0b7b3e7e0f30a010a,
title = "Progenitor cell-based treatment of glial disease",
abstract = "Diseases of glia, including astrocytes and oligodendrocytes, are among the most prevalent and disabling, yet least appreciated, conditions in neurology. In recent years, it has become clear that besides the overtly glial disorders of oligodendrocyte loss and myelin failure, such as the leukodystrophies and inflammatory demyelinations, a number of neurodegenerative and psychiatric disorders may also be causally linked to glial dysfunction and derive from astrocytic as well as oligodendrocytic pathology. The relative contribution of glial dysfunction to many of these disorders may be so great as to allow their treatment by the delivery of allogeneic glial progenitor cells, the precursors to both astroglia and myelin-producing oligodendrocytes. Given the development of new methods for producing and isolating these cells from pluripotent stem cells, both the myelin disorders and appropriate glial-based neurodegenerative conditions may now be compelling targets for cell-based therapy. As such, glial cell-based therapies may offer potential benefit to a broader range of diseases than ever before contemplated, including disorders such as Huntington's disease and the motor neuron degeneration of amyotrophic lateral sclerosis, which have traditionally been considered neuronal in nature.",
keywords = "Journal Article",
author = "Goldman, {Steven A}",
note = "{\textcopyright} 2017 Elsevier B.V. All rights reserved.",
year = "2017",
doi = "10.1016/bs.pbr.2017.02.010",
language = "English",
isbn = "978-0-12-813879-3",
volume = "231",
series = "Progress in Brain Research",
publisher = "Elsevier",
pages = "165--189",
booktitle = "Functional Neural Transplantation IV",

}

RIS

TY - CHAP

T1 - Progenitor cell-based treatment of glial disease

AU - Goldman, Steven A

N1 - © 2017 Elsevier B.V. All rights reserved.

PY - 2017

Y1 - 2017

N2 - Diseases of glia, including astrocytes and oligodendrocytes, are among the most prevalent and disabling, yet least appreciated, conditions in neurology. In recent years, it has become clear that besides the overtly glial disorders of oligodendrocyte loss and myelin failure, such as the leukodystrophies and inflammatory demyelinations, a number of neurodegenerative and psychiatric disorders may also be causally linked to glial dysfunction and derive from astrocytic as well as oligodendrocytic pathology. The relative contribution of glial dysfunction to many of these disorders may be so great as to allow their treatment by the delivery of allogeneic glial progenitor cells, the precursors to both astroglia and myelin-producing oligodendrocytes. Given the development of new methods for producing and isolating these cells from pluripotent stem cells, both the myelin disorders and appropriate glial-based neurodegenerative conditions may now be compelling targets for cell-based therapy. As such, glial cell-based therapies may offer potential benefit to a broader range of diseases than ever before contemplated, including disorders such as Huntington's disease and the motor neuron degeneration of amyotrophic lateral sclerosis, which have traditionally been considered neuronal in nature.

AB - Diseases of glia, including astrocytes and oligodendrocytes, are among the most prevalent and disabling, yet least appreciated, conditions in neurology. In recent years, it has become clear that besides the overtly glial disorders of oligodendrocyte loss and myelin failure, such as the leukodystrophies and inflammatory demyelinations, a number of neurodegenerative and psychiatric disorders may also be causally linked to glial dysfunction and derive from astrocytic as well as oligodendrocytic pathology. The relative contribution of glial dysfunction to many of these disorders may be so great as to allow their treatment by the delivery of allogeneic glial progenitor cells, the precursors to both astroglia and myelin-producing oligodendrocytes. Given the development of new methods for producing and isolating these cells from pluripotent stem cells, both the myelin disorders and appropriate glial-based neurodegenerative conditions may now be compelling targets for cell-based therapy. As such, glial cell-based therapies may offer potential benefit to a broader range of diseases than ever before contemplated, including disorders such as Huntington's disease and the motor neuron degeneration of amyotrophic lateral sclerosis, which have traditionally been considered neuronal in nature.

KW - Journal Article

U2 - 10.1016/bs.pbr.2017.02.010

DO - 10.1016/bs.pbr.2017.02.010

M3 - Book chapter

C2 - 28554396

SN - 978-0-12-813879-3

VL - 231

T3 - Progress in Brain Research

SP - 165

EP - 189

BT - Functional Neural Transplantation IV

CY - Cambridge, MA, United States

ER -

ID: 196377796