Injury to the Spinal Cord Niche Alters the Engraftment Dynamics of Human Neural Stem Cells
The microenvironment is a critical mediator of stem cell survival, proliferation, migration, and differentiation. The majority of preclinical studies involving transplantation of neural stem cells (NSCs) into the CNS have focused on injured or degenerating microenvironments, leaving a dearth of info...
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doaj-4130ad301f6c47aaa93ef09514384e252020-11-24T22:38:41ZengElsevierStem Cell Reports2213-67112014-05-012562063210.1016/j.stemcr.2014.03.005Injury to the Spinal Cord Niche Alters the Engraftment Dynamics of Human Neural Stem CellsChristopher J. Sontag0Nobuko Uchida1Brian J. Cummings2Aileen J. Anderson3Sue and Bill Gross Stem Cell Center, University of California, Irvine, Irvine, CA 92697, USAStem Cells, Inc., Newark, CA 94560, USASue and Bill Gross Stem Cell Center, University of California, Irvine, Irvine, CA 92697, USASue and Bill Gross Stem Cell Center, University of California, Irvine, Irvine, CA 92697, USAThe microenvironment is a critical mediator of stem cell survival, proliferation, migration, and differentiation. The majority of preclinical studies involving transplantation of neural stem cells (NSCs) into the CNS have focused on injured or degenerating microenvironments, leaving a dearth of information as to how NSCs differentially respond to intact versus damaged CNS. Furthermore, single, terminal histological endpoints predominate, providing limited insight into the spatiotemporal dynamics of NSC engraftment and migration. We investigated the early and long-term engraftment dynamics of human CNS stem cells propagated as neurospheres (hCNS-SCns) following transplantation into uninjured versus subacutely injured spinal cords of immunodeficient NOD-scid mice. We stereologically quantified engraftment, survival, proliferation, migration, and differentiation at 1, 7, 14, 28, and 98 days posttransplantation, and identified injury-dependent alterations. Notably, the injured microenvironment decreased hCNS-SCns survival, delayed and altered the location of proliferation, influenced both total and fate-specific migration, and promoted oligodendrocyte maturation.http://www.sciencedirect.com/science/article/pii/S2213671114000848 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Christopher J. Sontag Nobuko Uchida Brian J. Cummings Aileen J. Anderson |
spellingShingle |
Christopher J. Sontag Nobuko Uchida Brian J. Cummings Aileen J. Anderson Injury to the Spinal Cord Niche Alters the Engraftment Dynamics of Human Neural Stem Cells Stem Cell Reports |
author_facet |
Christopher J. Sontag Nobuko Uchida Brian J. Cummings Aileen J. Anderson |
author_sort |
Christopher J. Sontag |
title |
Injury to the Spinal Cord Niche Alters the Engraftment Dynamics of Human Neural Stem Cells |
title_short |
Injury to the Spinal Cord Niche Alters the Engraftment Dynamics of Human Neural Stem Cells |
title_full |
Injury to the Spinal Cord Niche Alters the Engraftment Dynamics of Human Neural Stem Cells |
title_fullStr |
Injury to the Spinal Cord Niche Alters the Engraftment Dynamics of Human Neural Stem Cells |
title_full_unstemmed |
Injury to the Spinal Cord Niche Alters the Engraftment Dynamics of Human Neural Stem Cells |
title_sort |
injury to the spinal cord niche alters the engraftment dynamics of human neural stem cells |
publisher |
Elsevier |
series |
Stem Cell Reports |
issn |
2213-6711 |
publishDate |
2014-05-01 |
description |
The microenvironment is a critical mediator of stem cell survival, proliferation, migration, and differentiation. The majority of preclinical studies involving transplantation of neural stem cells (NSCs) into the CNS have focused on injured or degenerating microenvironments, leaving a dearth of information as to how NSCs differentially respond to intact versus damaged CNS. Furthermore, single, terminal histological endpoints predominate, providing limited insight into the spatiotemporal dynamics of NSC engraftment and migration. We investigated the early and long-term engraftment dynamics of human CNS stem cells propagated as neurospheres (hCNS-SCns) following transplantation into uninjured versus subacutely injured spinal cords of immunodeficient NOD-scid mice. We stereologically quantified engraftment, survival, proliferation, migration, and differentiation at 1, 7, 14, 28, and 98 days posttransplantation, and identified injury-dependent alterations. Notably, the injured microenvironment decreased hCNS-SCns survival, delayed and altered the location of proliferation, influenced both total and fate-specific migration, and promoted oligodendrocyte maturation. |
url |
http://www.sciencedirect.com/science/article/pii/S2213671114000848 |
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