Academic Thesis

Basic information

Name Katayama Keiichi
Belonging department
Occupation name
researchmap researcher code B000305947
researchmap agency Okayama University of Science

Title

Enhanced expression of Pafah1b1 causes over-migration of cerebral cortical neurons into the marginal zone

Bibliography Type

 

Author

Kei-ichi Katayama
Kanehiro Hayashi
Seika Inoue
Kazushige Sakaguchi
Kazunori Nakajima

Summary

Mutations of PAFAH1B1 cause classical lissencephaly in humans. In addition, duplications and triplications of PAFAH1B1 are found in individuals with intellectual disability and other neurological disorders suggesting that proper brain development is highly sensitive to the PAFAH1B1 dosage. To examine the effect of PAFAH1B1 over-dosage in neural development, especially in migration of neurons and layer formation during cerebral cortical development, we overexpressed Pafah1b1 in migrating neurons in the mouse embryonic cortex using in utero electroporation. Enhanced expression of Pafah1b1 in radially-migrating neurons resulted in their over-migration into the marginal zone. Neurons that invaded the marginal zone were oriented abnormally. Layer distribution of Pafaha1b1-overexpressing neurons shifted more superficially than control neurons. Some of the Pafaha1b1-overexpressing future layer 4 neurons changed their positions to layers 2/3. Furthermore, they also changed their layer marker expression from layer 4 to layers 2/3. These results suggest that overexpression of Pafah1b1 affects the migration of neurons and disrupts layer formation in the developing cerebral cortex, and further support the idea that appropriate dosage of Pafah1b1 is crucial for the proper development of the brain.

Magazine(name)

BRAIN STRUCTURE & FUNCTION

Publisher

SPRINGER HEIDELBERG

Volume

222

Number Of Pages

9

StartingPage

4283

EndingPage

4291

Date of Issue

2017-12

Referee

Exist

Invited

Not exist

Language

English

Thesis Type

Research papers (academic journals)

ISSN

 

DOI

10.1007/s00429-017-1497-9

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PMID

 

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arXiv ID

 

ORCID Put Code

 

DBLP ID