Evidence map›Paper›PMID 31792065›Full record

ReviewDevelopment (Cambridge, England)2019

Awakening the regenerative potential of the mammalian retina.

James F Martin, Ross A Poché

Abstract readReview
In one paragraph

Review in Development (Cambridge, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Controlling donor and newborn neuron migration and maturation in the eye through microenvironment engineering.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  6. Article
  7. Direct neuronal reprogramming by temporal identity factors.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. Advances in the study of Müller glia reprogramming in mammals.Frontiers in cellular neuroscience · 2023
    Review
  9. Review
  10. Article
  11. Article
  12. Critical Examination of Müller Glia-DerivedFrontiers in cell and developmental biology · 2022
    Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Role of Macrophages and Microglia in Zebrafish Regeneration.International journal of molecular sciences · 2020
    Review
  18. Article
  19. 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

2 authors.

James F MartinDepartment of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX 77030, USA.
Ross A PochéDepartment of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX 77030, USA poche@bcm.edu.ORCID 0000-0002-5228-2383

Funding

Pitx2 in atrial fibrillationR01HL118761 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI MARTIN, JAMES F · 2014 to 2025
$6.1M
Hippo and Wnt Signaling in Cardiac RegenerationR01HL127717 · NHLBI · TEXAS HEART INSTITUTE · PI MARTIN, JAMES F · 2016 to 2023
$4.4M
Optical elastography for assessment of myocardial regenerationR01HL130804 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI LARIN, KIRILL V, MARTIN, JAMES F · 2016 to 2019
$2.9M
Transcriptional regulation of retinal mitochondrial function and cell cycleR01EY024906 · NEI · BAYLOR COLLEGE OF MEDICINE · PI POCHE, ROSS ANTHONY · 2015 to 2019
$2.3M
Hippo Pathway Regulation of Müller Glial Cell-mediated Retinal RegenerationR01EY030448 · NEI · BAYLOR COLLEGE OF MEDICINE · PI POCHE, ROSS ANTHONY · 2019 to 2022
$1.8M
NEI NIH HHS R01 EY024906NEI NIH HHS R01 EY030448NHLBI NIH HHS R01 HL118761NHLBI NIH HHS R01 HL127717NHLBI NIH HHS R01 HL130804
6 · The paper itself

Abstract

As with all glial cells, the major role of retinal Müller glia (MG) is to provide essential neuronal support. However, the MG of some non-mammalian species have the additional ability to generate new retinal neurons capable of sight restoration. Unfortunately, mammalian MG do not possess this ability. However, if we could understand the reasons why, we may be able to devise strategies to confer regenerative potential. The recent discovery that the Hippo signaling pathway acts as an intrinsic block to mammalian MG proliferation, along with reports of adeno-associated virus (AAV)-based MG reprogramming and functional photoreceptor differentiation, may indicate a watershed moment in the field of mammalian retinal regeneration. However, as researchers delve deeper into the cellular and molecular mechanisms, and further refine MG reprogramming strategies, we should recall past misinterpretations of data in this field and proceed with caution. Here, we provide a summary of these emerging data and a discussion of technical concerns specific to AAV-mediated reprogramming experiments that must be addressed in order for the field to move forward.

Indexed as

Cell ProliferationCellular ReprogrammingCellular Reprogramming TechniquesRegenerationAnimalsDependovirusEpendymoglial CellsGenetic VectorsHumansPhotoreceptor Cells, VertebrateCellular reprogrammingHippo signalingMüller gliaRetinal regeneration

Identifiers

PMID31792065
PMCPMC6918753

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.