4.5 Article

Pathophysiological analyses of periventricular nodular heterotopia using gyrencephalic mammals

Journal

HUMAN MOLECULAR GENETICS
Volume 26, Issue 6, Pages 1173-1181

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/hmg/ddx038

Keywords

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Funding

  1. Ministry of Education, Culture, Sports, Science and Technology
  2. Japan Agency for Medical Research and Development
  3. Life Science Foundation of Japan
  4. Senri Life Science Foundation
  5. Uehara Memorial Foundation
  6. Takeda Science Foundation
  7. Grants-in-Aid for Scientific Research [17H03541, 16H06822, 26111708] Funding Source: KAKEN

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Although periventricular nodular heterotopia (PNH) is often found in the cerebral cortex of people with thanatophoric dysplasia (TD), the pathophysiology of PNH in TD is largely unknown. This is mainly because of difficulties in obtaining brain samples of TD patients and a lack of appropriate animal models for analyzing the pathophysiology of PNH in TD. Here we investigate the pathophysiological mechanisms of PNH in the cerebral cortex of TD by utilizing a ferret TD model which we recently developed. To make TD ferrets, we electroporated fibroblast growth factor 8 (FGF8) into the cerebral cortex of ferrets. Our immunohistochemical analyses showed that PNH nodules in the cerebral cortex of TD ferrets were mostly composed of cortical neurons, including upper layer neurons and GABAergic neurons. We also found disorganizations of radial glial fibers and of the ventricular lining in the TD ferret cortex, indicating that PNH may result from defects in radial migration of cortical neurons along radial glial fibers during development. Our findings provide novel mechanistic insights into the pathogenesis of PNH in TD.

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