Cargando…

Astrocytes regulate adult hippocampal neurogenesis through ephrin-B signaling

Neurogenesis in the adult hippocampus involves activation of quiescent neural stem cells (NSCs) to yield transiently amplifying NSCs and progenitors, and ultimately neurons that affect learning and memory. This process is tightly controlled by microenvironmental cues, though few endogenous factors a...

Descripción completa

Detalles Bibliográficos
Autores principales: Ashton, Randolph S., Conway, Anthony, Pangarkar, Chinmay, Bergen, Jamie, Lim, Kwang-Il, Shah, Priya, Bissell, Mina, Schaffer, David V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458152/
https://www.ncbi.nlm.nih.gov/pubmed/22983209
http://dx.doi.org/10.1038/nn.3212
_version_ 1782244632515575808
author Ashton, Randolph S.
Conway, Anthony
Pangarkar, Chinmay
Bergen, Jamie
Lim, Kwang-Il
Shah, Priya
Bissell, Mina
Schaffer, David V.
author_facet Ashton, Randolph S.
Conway, Anthony
Pangarkar, Chinmay
Bergen, Jamie
Lim, Kwang-Il
Shah, Priya
Bissell, Mina
Schaffer, David V.
author_sort Ashton, Randolph S.
collection PubMed
description Neurogenesis in the adult hippocampus involves activation of quiescent neural stem cells (NSCs) to yield transiently amplifying NSCs and progenitors, and ultimately neurons that affect learning and memory. This process is tightly controlled by microenvironmental cues, though few endogenous factors are known to regulate neuronal differentiation. While astrocytes have been implicated, their role in juxtacrine (i.e. cell-cell contact-dependent) signaling within NSC niches has not been investigated. We show that ephrin-B2 presented from rodent hippocampal astrocytes regulates neurogenesis in vivo. Furthermore, clonal analysis in NSC fate-mapping studies reveals a novel role for ephrin-B2 in instructing neuronal differentiation. Additionally, ephrin-B2 signaling, transduced by EphB4 receptors on NSCs, activates β-catenin in vitro and in vivo independent of Wnt signaling and upregulates proneural transcription factors. Ephrin-B2(+) astrocytes thus promote neuronal differentiation of adult NSCs through juxtacrine signaling, findings that advance our understanding of adult neurogenesis and may have future regenerative medicine implications.
format Online
Article
Text
id pubmed-3458152
institution National Center for Biotechnology Information
language English
publishDate 2012
record_format MEDLINE/PubMed
spelling pubmed-34581522013-04-01 Astrocytes regulate adult hippocampal neurogenesis through ephrin-B signaling Ashton, Randolph S. Conway, Anthony Pangarkar, Chinmay Bergen, Jamie Lim, Kwang-Il Shah, Priya Bissell, Mina Schaffer, David V. Nat Neurosci Article Neurogenesis in the adult hippocampus involves activation of quiescent neural stem cells (NSCs) to yield transiently amplifying NSCs and progenitors, and ultimately neurons that affect learning and memory. This process is tightly controlled by microenvironmental cues, though few endogenous factors are known to regulate neuronal differentiation. While astrocytes have been implicated, their role in juxtacrine (i.e. cell-cell contact-dependent) signaling within NSC niches has not been investigated. We show that ephrin-B2 presented from rodent hippocampal astrocytes regulates neurogenesis in vivo. Furthermore, clonal analysis in NSC fate-mapping studies reveals a novel role for ephrin-B2 in instructing neuronal differentiation. Additionally, ephrin-B2 signaling, transduced by EphB4 receptors on NSCs, activates β-catenin in vitro and in vivo independent of Wnt signaling and upregulates proneural transcription factors. Ephrin-B2(+) astrocytes thus promote neuronal differentiation of adult NSCs through juxtacrine signaling, findings that advance our understanding of adult neurogenesis and may have future regenerative medicine implications. 2012-09-16 2012-10 /pmc/articles/PMC3458152/ /pubmed/22983209 http://dx.doi.org/10.1038/nn.3212 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Ashton, Randolph S.
Conway, Anthony
Pangarkar, Chinmay
Bergen, Jamie
Lim, Kwang-Il
Shah, Priya
Bissell, Mina
Schaffer, David V.
Astrocytes regulate adult hippocampal neurogenesis through ephrin-B signaling
title Astrocytes regulate adult hippocampal neurogenesis through ephrin-B signaling
title_full Astrocytes regulate adult hippocampal neurogenesis through ephrin-B signaling
title_fullStr Astrocytes regulate adult hippocampal neurogenesis through ephrin-B signaling
title_full_unstemmed Astrocytes regulate adult hippocampal neurogenesis through ephrin-B signaling
title_short Astrocytes regulate adult hippocampal neurogenesis through ephrin-B signaling
title_sort astrocytes regulate adult hippocampal neurogenesis through ephrin-b signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458152/
https://www.ncbi.nlm.nih.gov/pubmed/22983209
http://dx.doi.org/10.1038/nn.3212
work_keys_str_mv AT ashtonrandolphs astrocytesregulateadulthippocampalneurogenesisthroughephrinbsignaling
AT conwayanthony astrocytesregulateadulthippocampalneurogenesisthroughephrinbsignaling
AT pangarkarchinmay astrocytesregulateadulthippocampalneurogenesisthroughephrinbsignaling
AT bergenjamie astrocytesregulateadulthippocampalneurogenesisthroughephrinbsignaling
AT limkwangil astrocytesregulateadulthippocampalneurogenesisthroughephrinbsignaling
AT shahpriya astrocytesregulateadulthippocampalneurogenesisthroughephrinbsignaling
AT bissellmina astrocytesregulateadulthippocampalneurogenesisthroughephrinbsignaling
AT schafferdavidv astrocytesregulateadulthippocampalneurogenesisthroughephrinbsignaling