Divergent roles of ApoER2 and Vldlr in the migration of cortical neurons.

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Divergent roles of ApoER2 and Vldlr in the migration of cortical neurons. / Hack, Iris; Hellwig, Sabine; Junghans, Dirk; Brunne, Bianka; Bock, Hans H; Zhao, Shanting; Frotscher, Michael.

In: DEVELOPMENT, Vol. 134, No. 21, 21, 2007, p. 3883-3891.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Hack, I, Hellwig, S, Junghans, D, Brunne, B, Bock, HH, Zhao, S & Frotscher, M 2007, 'Divergent roles of ApoER2 and Vldlr in the migration of cortical neurons.', DEVELOPMENT, vol. 134, no. 21, 21, pp. 3883-3891. <http://www.ncbi.nlm.nih.gov/pubmed/17913789?dopt=Citation>

APA

Hack, I., Hellwig, S., Junghans, D., Brunne, B., Bock, H. H., Zhao, S., & Frotscher, M. (2007). Divergent roles of ApoER2 and Vldlr in the migration of cortical neurons. DEVELOPMENT, 134(21), 3883-3891. [21]. http://www.ncbi.nlm.nih.gov/pubmed/17913789?dopt=Citation

Vancouver

Hack I, Hellwig S, Junghans D, Brunne B, Bock HH, Zhao S et al. Divergent roles of ApoER2 and Vldlr in the migration of cortical neurons. DEVELOPMENT. 2007;134(21):3883-3891. 21.

Bibtex

@article{8d95f06dc40b4550ba390b83c35a19ad,
title = "Divergent roles of ApoER2 and Vldlr in the migration of cortical neurons.",
abstract = "Reelin, its lipoprotein receptors [very low density lipoprotein receptor (Vldlr) and apolipoprotein E receptor 2 (ApoER2; also known as Lrp8)], and the cytoplasmic adaptor protein disabled 1 (Dab1) are important for the correct formation of layers in the cerebral cortex. Reeler mice lacking the reelin protein show altered radial neuronal migration resulting in an inversion of cortical layers. ApoER2 Vldlr double-knockout mutants and Dab1 mutants show a reeler-like phenotype, whereas milder phenotypes are found if only one of the two lipoprotein receptors for reelin is absent. However, the precise role of the individual reelin receptors in neuronal migration remained unclear. In the study reported here, we performed fate mapping of newly generated cortical neurons in single and double receptor mutants using bromodeoxyuridine-labeling and layer-specific markers. We present evidence for divergent roles of the two reelin receptors Vldlr and ApoER2, with Vldlr mediating a stop signal for migrating neurons and ApoER2 being essential for the migration of late generated neocortical neurons.",
keywords = "Animals, Mice, Mice, Knockout, Cell Movement, Mutation genetics, Gene Expression Regulation, Developmental, DNA-Binding Proteins metabolism, Neuroglia metabolism, Neurons cytology, Receptors, LDL deficiency, Receptors, Lipoprotein deficiency, Repressor Proteins metabolism, Transcription, Genetic genetics, Animals, Mice, Mice, Knockout, Cell Movement, Mutation genetics, Gene Expression Regulation, Developmental, DNA-Binding Proteins metabolism, Neuroglia metabolism, Neurons cytology, Receptors, LDL deficiency, Receptors, Lipoprotein deficiency, Repressor Proteins metabolism, Transcription, Genetic genetics",
author = "Iris Hack and Sabine Hellwig and Dirk Junghans and Bianka Brunne and Bock, {Hans H} and Shanting Zhao and Michael Frotscher",
year = "2007",
language = "Deutsch",
volume = "134",
pages = "3883--3891",
journal = "DEVELOPMENT",
issn = "0950-1991",
publisher = "Company of Biologists Ltd",
number = "21",

}

RIS

TY - JOUR

T1 - Divergent roles of ApoER2 and Vldlr in the migration of cortical neurons.

AU - Hack, Iris

AU - Hellwig, Sabine

AU - Junghans, Dirk

AU - Brunne, Bianka

AU - Bock, Hans H

AU - Zhao, Shanting

AU - Frotscher, Michael

PY - 2007

Y1 - 2007

N2 - Reelin, its lipoprotein receptors [very low density lipoprotein receptor (Vldlr) and apolipoprotein E receptor 2 (ApoER2; also known as Lrp8)], and the cytoplasmic adaptor protein disabled 1 (Dab1) are important for the correct formation of layers in the cerebral cortex. Reeler mice lacking the reelin protein show altered radial neuronal migration resulting in an inversion of cortical layers. ApoER2 Vldlr double-knockout mutants and Dab1 mutants show a reeler-like phenotype, whereas milder phenotypes are found if only one of the two lipoprotein receptors for reelin is absent. However, the precise role of the individual reelin receptors in neuronal migration remained unclear. In the study reported here, we performed fate mapping of newly generated cortical neurons in single and double receptor mutants using bromodeoxyuridine-labeling and layer-specific markers. We present evidence for divergent roles of the two reelin receptors Vldlr and ApoER2, with Vldlr mediating a stop signal for migrating neurons and ApoER2 being essential for the migration of late generated neocortical neurons.

AB - Reelin, its lipoprotein receptors [very low density lipoprotein receptor (Vldlr) and apolipoprotein E receptor 2 (ApoER2; also known as Lrp8)], and the cytoplasmic adaptor protein disabled 1 (Dab1) are important for the correct formation of layers in the cerebral cortex. Reeler mice lacking the reelin protein show altered radial neuronal migration resulting in an inversion of cortical layers. ApoER2 Vldlr double-knockout mutants and Dab1 mutants show a reeler-like phenotype, whereas milder phenotypes are found if only one of the two lipoprotein receptors for reelin is absent. However, the precise role of the individual reelin receptors in neuronal migration remained unclear. In the study reported here, we performed fate mapping of newly generated cortical neurons in single and double receptor mutants using bromodeoxyuridine-labeling and layer-specific markers. We present evidence for divergent roles of the two reelin receptors Vldlr and ApoER2, with Vldlr mediating a stop signal for migrating neurons and ApoER2 being essential for the migration of late generated neocortical neurons.

KW - Animals

KW - Mice

KW - Mice, Knockout

KW - Cell Movement

KW - Mutation genetics

KW - Gene Expression Regulation, Developmental

KW - DNA-Binding Proteins metabolism

KW - Neuroglia metabolism

KW - Neurons cytology

KW - Receptors, LDL deficiency

KW - Receptors, Lipoprotein deficiency

KW - Repressor Proteins metabolism

KW - Transcription, Genetic genetics

KW - Animals

KW - Mice

KW - Mice, Knockout

KW - Cell Movement

KW - Mutation genetics

KW - Gene Expression Regulation, Developmental

KW - DNA-Binding Proteins metabolism

KW - Neuroglia metabolism

KW - Neurons cytology

KW - Receptors, LDL deficiency

KW - Receptors, Lipoprotein deficiency

KW - Repressor Proteins metabolism

KW - Transcription, Genetic genetics

M3 - SCORING: Zeitschriftenaufsatz

VL - 134

SP - 3883

EP - 3891

JO - DEVELOPMENT

JF - DEVELOPMENT

SN - 0950-1991

IS - 21

M1 - 21

ER -