Evidence map›Paper›PMID 29178409›Full record

ArticleGlia2018

Sox2 regulates astrocytic and vascular development in the retina.

Amanda G Kautzman, Patrick W Keeley, Michael M Nahmou, Gabriel Luna, Steven K Fisher, Benjamin E Reese

Abstract read
In one paragraph

Article in Glia, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. NRLStem cells (Dayton, Ohio) · 2021
    Article
  9. Article
  10. The optic nerve lamina region is a neural progenitor cell niche.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  11. Article
  12. Article
  13. Review
  14. AAVProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  15. Article
  16. Article
  17. 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

6 authors at 1 institution in 1 country.

Amanda G KautzmanNeuroscience Research Institute, University of California at Santa Barbara, Santa Barbara, CA, 93106-5060.ORCID 0000-0001-7010-6669
Patrick W KeeleyNeuroscience Research Institute, University of California at Santa Barbara, Santa Barbara, CA, 93106-5060.ORCID 0000-0003-1260-498X
Michael M NahmouNeuroscience Research Institute, University of California at Santa Barbara, Santa Barbara, CA, 93106-5060.
Gabriel LunaNeuroscience Research Institute, University of California at Santa Barbara, Santa Barbara, CA, 93106-5060.
Steven K FisherNeuroscience Research Institute, University of California at Santa Barbara, Santa Barbara, CA, 93106-5060.
Benjamin E ReeseNeuroscience Research Institute, University of California at Santa Barbara, Santa Barbara, CA, 93106-5060.
University of California, Santa Barbara · US

Funding

Development of Retinal Bipolar CellsR01EY019968 · NEI · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI REESE, BENJAMIN E · 2010 to 2023
$4.9M
Spectral Laser Scanning Biological MicroscopeS10OD010610 · OD · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI RAVEN, MARY A · 2012 to 2012
$429k
NEI NIH HHS R01 EY019968NIH HHS S10 OD010610
6 · The paper itself

Abstract

Sox2 is a transcriptional regulator that is highly expressed in retinal astrocytes, yet its function in these cells has not previously been examined. To understand its role, we conditionally deleted Sox2 from the population of astrocytes and examined the consequences on retinal development. We found that Sox2 deletion does not alter the migration of astrocytes, but it impairs their maturation, evidenced by the delayed upregulation of glial fibrillary acidic protein (GFAP) across the retina. The centro-peripheral gradient of angiogenesis is also delayed in Sox2-CKO retinas. In the mature retina, we observed lasting abnormalities in the astrocytic population evidenced by the sporadic loss of GFAP immunoreactivity in the peripheral retina as well as by the aberrant extension of processes into the inner retina. Blood vessels in the adult retina are also under-developed and show a decrease in the frequency of branch points and in total vessel length. The developmental relationship between maturing astrocytes and angiogenesis suggests a causal relationship between the astrocytic loss of Sox2 and the vascular architecture in maturity. We suggest that the delay in astrocytic maturation and vascular invasion may render the retina hypoxic, thereby causing the abnormalities we observe in adulthood. These studies uncover a novel role for Sox2 in the development of retinal astrocytes and indicate that its removal can lead to lasting changes to retinal homeostasis.

Indexed as

AnimalsAstrocytesGlial Fibrillary Acidic ProteinMice, TransgenicRetinaRetinal VesselsSOXB1 Transcription FactorsGlial Fibrillary Acidic Proteinglial fibrillary astrocytic protein, mouseSox2 protein, mouseSOXB1 Transcription Factorsangiogenesisastrocyteblood vesselscollagenGFAPvasculature

Identifiers

PMID29178409
PMCPMC5767138
OpenAlexW2770926586

What OpenQuestion holds

Textmetadata
LicenceTDM
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.