Skip to main content

Advertisement

Log in

Dentate granule progenitor cell properties are rapidly altered soon after birth

  • Original Article
  • Published:
Brain Structure and Function Aims and scope Submit manuscript

A Correction to this article was published on 25 January 2018

This article has been updated

Abstract

Neurogenesis occurs during the embryonic period and ceases soon after birth in the neocortex, but continues to occur in the hippocampus even in the adult. The embryonic neocortex has radial glia or progenitor cells expressing brain lipid-binding protein (BLBP), whereas the adult hippocampus has radial granule progenitor cells expressing BLBP and glial fibrillary acidic protein (GFAP) in the subgranular zone. We previously found that embryonic hippocampal granule progenitor cells express GFAP, but not BLBP, indicating that these cells are different from both embryonic neocortical and adult granule progenitor cells. In the present study, as the first step towards understanding the mechanism of persistent hippocampal neurogenesis, we aimed to determine the stage at which embryonic-type granule progenitors become adult-type progenitors using mouse Gfap-GFP transgenic mice. During the embryonic stages, Gfap-GFP-positive (Gfap-GFP+) cells were distributed in the entire developing dentate gyrus (DG), whereas BLBP-positive (BLBP+) cells were mainly present in the fimbria and subpial region, and to some extent in the DG. Up to postnatal day 0 (P0), double-positive cells were scarcely detected. However, at P1, one-third of the Gfap-GFP+ cells in the DG suddenly began to weakly express BLBP. Thereafter, Gfap-GFP+/BLBP+ cells rapidly increased in number, and extended their radial processes in the inner granular cell layer. At P14 and in the adult, two-thirds of the Gfap-GFP+ cells in the subgranular zone showed BLBP immunoreactivity. These results suggest that the properties of hippocampal granule progenitor cells are rapidly altered from an embryonic to adult type soon after birth.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
EUR 32.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or Ebook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9

We’re sorry, something doesn't seem to be working properly.

Please try refreshing the page. If that doesn't work, please contact support so we can address the problem.

Change history

  • 25 January 2018

    In the original publication figure parts 8c, 8f, and 8i were mixed up and thus incorrectly labeled. Here is a corrected version with the parts properly labeled

References

Download references

Acknowledgements

We thank Ryusuke Suzuki for the generation of mGfap-GFP mice. We also thank Dr. Helena Popiel of the Department of International Medical Communications of Tokyo Medical University for editorial review of the manuscript. This work was supported by funding from Japan Society for the Promotion of Science (JSPS) KAKENHI (Grant numbers 22500306, 25430041, and 16K07033).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Tatsunori Seki.

Ethics declarations

Conflict of interest

The authors have no conflicts of interest associated with this study.

Additional information

A correction to this article is available online at https://doi.org/10.1007/s00429-018-1613-5.

Electronic supplementary material

Below is the link to the electronic supplementary material.

429_2017_1499_MOESM1_ESM.tif

Supplemental figure Expression of mGfap-GFP and BLPB at P0.Some mGfap-GFP+ cells express BLBP very weakly, although in most sections mGfap-GFP+/BLBP+ cells are not observed (See Fig. 2). Arrows indicate mGfap-GFP+/BLBP+ cells. Scale bars 50 µm (a-c) (TIFF 8987 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Matsue, K., Minakawa, S., Kashiwagi, T. et al. Dentate granule progenitor cell properties are rapidly altered soon after birth. Brain Struct Funct 223, 357–369 (2018). https://doi.org/10.1007/s00429-017-1499-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00429-017-1499-7

Keywords

Navigation