erbB3 is dispensable for oligodendrocyte development in vitro and in vivo
erbB3 is dispensable for oligodendrocyte development in vitro and in vivo
During development and in the adult, erbB2, erbB3, and erbB4 are expressed in many tissues and as heterodimers (B2/B3, B2/B4) serve as receptors for neuregulins. The general importance of neuregulin receptors for development is underlined by the observed embryonic (erbB2, erbB4) or perinatal (erbB3) lethality in mouse mutants. These mutants further revealed the fundamental role of the erbB2/erbB3 heterodimer for proper Schwann cell development, the ensheathing glia of the peripheral nervous system. However, only little is known about the functions of neuregulins and their receptors during postnatal development and in the adult. erbB2 and erbB3 during late embryogenesis and postnatally are expressed in different areas and cell types of the central nervous system, including oligodendrocytes, the ensheathing glia of the central nervous system. As terminal differentiation of oligodendrocytes peaks during postnatal development, it is not possible to use the neuregulin receptor mouse mutants to study terminal differentiation of oligodendrocytes in their absence in vivo. In order to investigate possible functions of the erbB3 gene in oligodendrocytes, we employed two different techniques. First, we directed the differentiation of erbB3-deficient embryonic stem cells into neural cell types to analyze the development of oligodendrocytes in the absence of erbB3 in vitro. Second, we grafted neural stem cells from spinal cords of erbB3 mutants into the retina of young mice to monitor oligodendrocyte differentiation and myelination in vivo. Results of both experimental approaches clearly show that erbB3 is not required for normal oligodendrocyte development and myelination.
nerve fibers, metabolism, cytology, male, role, surgery, mice, adult, transplantation, embryology, stem-cells, fetus, animals, neuregulins, receptor, ultrastructure
67-75
Schmucker, Johannes
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Ader, Marius
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Brockschnieder, Damian
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Brodarac, Andreja
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Bartsch, Udo
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Riethmacher, Dieter
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26 June 2003
Schmucker, Johannes
daa1fd68-ecfa-448f-bcf4-410d6a99f3c2
Ader, Marius
c9f648df-e397-4af1-a5f9-6893e2811a92
Brockschnieder, Damian
fc5b07e0-7c18-4084-ba59-b10f8ba045ef
Brodarac, Andreja
665b9bf9-df4f-43cf-ac6f-7cd9b596a834
Bartsch, Udo
a0292695-52cc-493c-9dd4-f8fdb0f4097f
Riethmacher, Dieter
1a0a0c2e-e94d-4d0a-a890-90107a2545bc
Schmucker, Johannes, Ader, Marius, Brockschnieder, Damian, Brodarac, Andreja, Bartsch, Udo and Riethmacher, Dieter
(2003)
erbB3 is dispensable for oligodendrocyte development in vitro and in vivo.
GLIA, 44 (1), .
(doi:10.1002/glia.10275).
Abstract
During development and in the adult, erbB2, erbB3, and erbB4 are expressed in many tissues and as heterodimers (B2/B3, B2/B4) serve as receptors for neuregulins. The general importance of neuregulin receptors for development is underlined by the observed embryonic (erbB2, erbB4) or perinatal (erbB3) lethality in mouse mutants. These mutants further revealed the fundamental role of the erbB2/erbB3 heterodimer for proper Schwann cell development, the ensheathing glia of the peripheral nervous system. However, only little is known about the functions of neuregulins and their receptors during postnatal development and in the adult. erbB2 and erbB3 during late embryogenesis and postnatally are expressed in different areas and cell types of the central nervous system, including oligodendrocytes, the ensheathing glia of the central nervous system. As terminal differentiation of oligodendrocytes peaks during postnatal development, it is not possible to use the neuregulin receptor mouse mutants to study terminal differentiation of oligodendrocytes in their absence in vivo. In order to investigate possible functions of the erbB3 gene in oligodendrocytes, we employed two different techniques. First, we directed the differentiation of erbB3-deficient embryonic stem cells into neural cell types to analyze the development of oligodendrocytes in the absence of erbB3 in vitro. Second, we grafted neural stem cells from spinal cords of erbB3 mutants into the retina of young mice to monitor oligodendrocyte differentiation and myelination in vivo. Results of both experimental approaches clearly show that erbB3 is not required for normal oligodendrocyte development and myelination.
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Published date: 26 June 2003
Keywords:
nerve fibers, metabolism, cytology, male, role, surgery, mice, adult, transplantation, embryology, stem-cells, fetus, animals, neuregulins, receptor, ultrastructure
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Local EPrints ID: 60212
URI: http://eprints.soton.ac.uk/id/eprint/60212
ISSN: 0894-1491
PURE UUID: 09876654-c1a6-42e3-9fa8-c6b265e1a430
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Date deposited: 08 Sep 2008
Last modified: 16 Mar 2024 03:56
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Author:
Johannes Schmucker
Author:
Marius Ader
Author:
Damian Brockschnieder
Author:
Andreja Brodarac
Author:
Udo Bartsch
Author:
Dieter Riethmacher
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