4.6 Article

Intermediate Neuronal Progenitors (Basal Progenitors) Produce Pyramidal-Projection Neurons for All Layers of Cerebral Cortex

Journal

CEREBRAL CORTEX
Volume 19, Issue 10, Pages 2439-2450

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/cercor/bhn260

Keywords

Eomes; intermediate progenitor cells; Pax6; radial glia; Tbr2

Categories

Funding

  1. National Institutes of Health [K02 NS045018, R01 NS050248]
  2. Deutsche Forschungsgemeinschaft [SPP 1109 Hu 275/7-3, SPP 1111 Hu 275/8-3, SFB/TR 13 B1, SFB 655 A2]
  3. Deutsche Forschungsgemeinschaft
  4. Fonds der Chemischen Industrie
  5. Federal Ministry of Education and Research [NGFN-2, 01GR0402, PRI-S08T05]
  6. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS050248, K02NS045018] Funding Source: NIH RePORTER

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The developing cerebral cortex contains apical and basal types of neurogenic progenitor cells. Here, we investigated the cellular properties and neurogenic output of basal progenitors, also called intermediate neuronal progenitors (INPs). We found that basal mitoses expressing transcription factor Tbr2 (an INP marker) were present throughout corticogenesis, from embryonic day 10.5 through birth. Postnatally, Tbr2(+) progenitors were present in the dentate gyrus, subventricular zone (SVZ), and posterior periventricle (pPV). Two morphological subtypes of INPs were distinguished in the embryonic cortex, short radial'' in the ventricular zone (VZ) and multipolar in the SVZ, probably corresponding to molecularly defined INP subtypes. Unexpectedly, many short radial INPs appeared to contact the apical (ventricular) surface and some divided there. Time-lapse video microscopy suggested that apical INP divisions produced daughter INPs. Analysis of neurogenic divisions (Tis21-green fluorescent protein [GFP](+)) indicated that INPs may produce the majority of projection neurons for preplate, deep, and superficial layers. Conversely, proliferative INP divisions (Tis21-GFP(-)) increased from early to middle corticogenesis, concomitant with SVZ growth. Our findings support the hypothesis that regulated amplification of INPs may be an important factor controlling the balance of neurogenesis among different cortical layers.

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