Evidence map›Paper›PMID 24166578›Full record

ArticleThe Journal of comparative neurology2014

Distinct physiological and developmental properties of hippocampal CA2 subfield revealed by using anti-Purkinje cell protein 4 (PCP4) immunostaining.

Andrew San Antonio, Kristopher Liban, Taruna Ikrar, Eugene Tsyganovskiy, Xiangmin Xu

Abstract read
In one paragraph

Article in The Journal of comparative neurology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

43 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Andrew San AntonioDepartment of Anatomy and Neurobiology, School of Medicine, University of California, Irvine, California, 92697-1275.
Kristopher Liban
Taruna Ikrar
Eugene Tsyganovskiy
Xiangmin Xu

Funding

Hippocampal inhibitory neuronal circuit organizationR01NS078434 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI XU, XIANGMIN · 2012 to 2016
$1.6M
Local Connections and In Vivo Physiology of Inhibitory Cortical NeuronsR00DA023700 · NIDA · UNIVERSITY OF CALIFORNIA-IRVINE · PI XU, XIANGMIN · 2008 to 2010
$1.1M
NIDA NIH HHS DA023700NIDA NIH HHS R00 DA023700NINDS NIH HHS NS078434NINDS NIH HHS R01 NS078434
6 · The paper itself

Abstract

The hippocampal CA2 subfield was initially identified by Lorente de Nó as an anatomically distinct region based on its cytoarchitectural features. Although there is an enormous body of literature on other hippocampal subfields (CA1 and CA3), relatively little is known about the physiological and developmental properties of CA2. Here we report identification of the CA2 region in the mouse by immunostaining with a Purkinje cell protein 4 (PCP4) antibody, which effectively delineates CA3/CA2 and CA2/CA1 borders and agrees well with previous cytoarchitectural definitions of CA2. The PCP4 immunostaining-delineated CA2 neurons have distinguishable differences in cell morphology, physiology, and synaptic circuit connections compared with distal CA3 and proximal CA1 regions. The average somatic sizes of excitatory cells differ across CA1-3, with the smallest to largest somatic size being CA1<CA2<CA3. CA2 excitatory cells have dense dendritic spines, but do not have thorny excrescences associated with bordering CA3 neurons. Photostimulation functional circuit mapping shows that CA2 excitatory neurons receives extensive synaptic input from CA3, but no detectable input from the dentate gyrus. CA2 excitatory cells also differ significantly from CA3 cells in intrinsic electrophysiological parameters, such as membrane capacitance and spiking rates. Although CA2 neurons differ from CA1 neurons for PCP4 and other marker expressions, these neurons have less distinct neurophysiological and morphological properties. Developmental examination revealed that PCP4 immunostaining first appears at postnatal day 4-5 and becomes successively more refined around CA2 until reaching adult form by postnatal day 21.

Indexed as

Analysis of VarianceAnimalsAnimals, NewbornCA2 Region, HippocampalCalbindin 2Calcium-Binding ProteinsElectric StimulationExcitatory Postsynaptic PotentialsFibroblast Growth Factor 2Gene Expression RegulationIn Vitro TechniquesLuminescent ProteinsMembrane PotentialsMiceMice, Inbred C57BLMice, TransgenicCalb2 protein, mouseCalbindin 2Calcium-Binding ProteinsFibroblast Growth Factor 2Luminescent ProteinsNerve Tissue ProteinsPcp4 protein, mousecircuit mappingelectrophysiologyimmunochemical

Identifiers

PMID24166578
PMCPMC4001794

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.