Evidence map›Paper›PMID 31379509›Full record

ArticleFrontiers in cellular neuroscience2019

Caveolin-1 Phosphorylation Is Essential for Axonal Growth of Human Neurons Derived From iPSCs.

Shanshan Wang, Zheng Zhang, Angels Almenar-Queralt, Joseph Leem, Celine DerMardirossian, David M Roth, Piyush M Patel, Hemal H Patel, Brian P Head

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

10 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Caveolae: Metabolic Platforms at the Crossroads of Health and Disease.International journal of molecular sciences · 2025
    Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Caveolin1: its roles in normal and cancer stem cells.Journal of cancer research and clinical oncology · 2021
    Review
  9. Article
  10. Caveolae as Potential Hijackable Gates in Cell Communication.Frontiers in cell and developmental biology · 2020
    Review
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

9 authors at 4 institutions in 1 country.

Shanshan WangVeterans Affairs San Diego Healthcare System, San Diego, CA, United States.
Zheng ZhangVeterans Affairs San Diego Healthcare System, San Diego, CA, United States.
Angels Almenar-QueraltDepartment of Cellular and Molecular Medicine, Sanford Consortium for Regenerative Medicine, La Jolla, CA, United States.
Joseph LeemVeterans Affairs San Diego Healthcare System, San Diego, CA, United States.
Celine DerMardirossianDepartment of Immunology and Microbial Sciences, The Scripps Research Institute, La Jolla, CA, United States.
David M RothVeterans Affairs San Diego Healthcare System, San Diego, CA, United States.
Piyush M PatelVeterans Affairs San Diego Healthcare System, San Diego, CA, United States.
Hemal H PatelVeterans Affairs San Diego Healthcare System, San Diego, CA, United States.
Brian P HeadVeterans Affairs San Diego Healthcare System, San Diego, CA, United States.
University of California, San Diego · USVA San Diego Healthcare System · USSanford Consortium for Regenerative Medicine · USScripps Research Institute · US

Funding

Caveolae, mitochondria, and cardiac protection.R01HL091071 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI PATEL, HEMAL H · 2008 to 2019
$3.8M
Protection of the Aged MyocardiumR01HL107200 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI PATEL, HEMAL H, ROTH, DAVID M · 2011 to 2014
$2.1M
Neuronal-targeted caveolin-1 as a therapy for traumatic brain injuryR01NS073653 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HEAD, BRIAN P · 2012 to 2015
$1.4M
Novel Therapeutics for Diabetic CardiomyopathyI01BX001963 · VA · VA SAN DIEGO HEALTHCARE SYSTEM · PI PATEL, HEMAL H · 2013 to 2025
–
Caveolin-Mediated Neuroplasticity in Alzheimer's Disease and in Human Neurons Harboring EOFAD MutationsI01BX003671 · VA · VA SAN DIEGO HEALTHCARE SYSTEM · PI HEAD, BRIAN P · 2017 to 2024
–
BLRD VA I01 BX001963BLRD VA I01 BX003671NHLBI NIH HHS R01 HL091071NHLBI NIH HHS R01 HL107200NINDS NIH HHS R01 NS073653
6 · The paper itself

Abstract

Proper axonal growth and guidance is essential for neuron differentiation and development. Abnormal neuronal development due to genetic or epigenetic influences can contribute to neurological and mental disorders such as Down syndrome, Rett syndrome, and autism. Identification of the molecular targets that promote proper neuronal growth and differentiation may restore structural and functional neuroplasticity, thus improving functional performance in neurodevelopmental disorders. Using differentiated human neuronal progenitor cells (NPCs) derived from induced pluripotent stem cells (iPSCs), the present study demonstrates that during early stage differentiation of human NPCs, neuron-targeted overexpression constitutively active Rac1 (Rac1CA) and constitutively active Cdc42 (Cdc42CA) enhance expression of P-Cav-1, T-Cav-1, and P-cofilin and increases axonal growth. Similarly, neuron-targeted over-expression of Cav-1 (termed

Indexed as

axonal growthcaveolin-1iPSCsNPCsphosphorylationRac1/Cdc42

Identifiers

PMID31379509
PMCPMC6650578
OpenAlexW2959432411

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.