Evidence map›Paper›PMID 23536091›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2013

The α crystallin domain of small heat shock protein b8 (Hspb8) acts as survival and differentiation factor in adult hippocampal neurogenesis.

Gerardo Ramírez-Rodríguez, Harish Babu, Friederike Klempin, Olga Krylyshkina, Veerle Baekelandt, Rik Gijsbers, Zeger Debyser, Rupert W Overall, Zeina Nicola, Klaus Fabel and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
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

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. CSPα in neurodegenerative diseases.Frontiers in aging neuroscience · 2022
    Review
  7. Review
  8. Article
  9. Loss of postnatal quiescence of neural stem cells through mTOR activation upon genetic removal of cysteine string protein-α.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Neurogenesis in the Adult Hippocampus.Cold Spring Harbor perspectives in biology · 2015
    Review
  16. 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

11 authors at 6 institutions in 5 countries.

Gerardo Ramírez-RodríguezLaboratory of Neurogenesis, Division of Clinical Investigations, National Institute of Psychiatry Ramón de la Fuente Muñiz, 14370 México, DF México.
Harish Babu
Friederike Klempin
Olga Krylyshkina
Veerle Baekelandt
Rik Gijsbers
Zeger Debyser
Rupert W Overall
Zeina Nicola
Klaus Fabel
Gerd Kempermann
Gene Therapy Laboratory · FRGerman Center for Neurodegenerative Diseases · DEKU Leuven · BEInstituto Nacional de Psiquiatría · MXStanford University · USUniversity of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adult hippocampal neurogenesis is to a large degree controlled at the level of cell survival, and a number of potential mediators of this effect have been postulated. Here, we investigated the small heat shock protein Hspb8, which, because of its pleiotropic prosurvival effects in other systems, was considered a particularly promising candidate factor. Hspb8 is, for example, found in plaques of Alzheimer disease but exerts neuroprotective effects. We found that expression of Hspb8 increased during differentiation in vitro and was particularly associated with later stages (48-96 h) of differentiation. Gain-of-function and loss-of-function experiments supported the hypothesis that Hspb8 regulates cell survival of new neurons in vitro. In the dentate gyrus of adult mice in vivo, lentiviral overexpression of Hspb8 doubled the surviving cells and concomitantly promoted differentiation and net neurogenesis without affecting precursor cell proliferation. We also discovered that the truncated form of the crystallin domain of Hspb8 was sufficient to affect cell survival and neuronal differentiation in vitro and in vivo. Precursor cell experiments in vitro revealed that Hspb8 increases the phosphorylation of Akt and suggested that the prosurvival effect can be produced by a cell-autonomous mechanism. Analysis of hippocampal Hspb8 expression in mice of 69 strains of the recombinant inbred set BXD revealed that Hspb8 is a cis-acting gene whose expression was associated with clusters of transcript enriched in genes linked to growth factor signaling and apoptosis. Our results strongly suggest that Hspb8 and its α-crystallin domain might act as pleiotropic prosurvival factor in the adult hippocampus.

Indexed as

Adult Stem Cellsalpha-CrystallinsAnalysis of VarianceAnimalsBromodeoxyuridineCell DifferentiationCell ProliferationCell SurvivalComputational BiologyDentate GyrusFemaleGene Expression RegulationGenetic VectorsGreen Fluorescent ProteinsHeat-Shock Proteins, SmallMicealpha-CrystallinsBromodeoxyuridineenhanced green fluorescent proteinGreen Fluorescent ProteinsHeat-Shock Proteins, SmallNerve Growth FactorsNerve Tissue ProteinsRNA, MessengerS100 Calcium Binding Protein beta SubunitS100 Proteins

Identifiers

PMID23536091
PMCPMC6705050
OpenAlexW2062388510

What OpenQuestion holds

Textmetadata
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.