Evidence map›Paper›PMID 32896271›Full record

ArticleeLife2020

Direct reprogramming of human smooth muscle and vascular endothelial cells reveals defects associated with aging and Hutchinson-Gilford progeria syndrome.

Simone Bersini, Roberta Schulte, Ling Huang, Hannah Tsai, Martin W Hetzer

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

23 citing papers in PubMed, 33 citations in OpenAlex.

  1. Direct in vivo reprogramming to relieve tissue ischemia via induced vasculogenesis.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  2. Review
  3. Article
  4. In Vitro Modeling of Vascular Senescence.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Generation of Directly Reprogrammed Human Endothelial Cells.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  11. Engineering Organ-on-a-Chip Systems for Vascular Diseases.Arteriosclerosis, thrombosis, and vascular biology · 2023
    Review
  12. Endothelial cell direct reprogramming: Past, present, and future.Journal of molecular and cellular cardiology · 2023
    Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Beyond Static Pipes: Mechanisms and In Vitro Models of Vascular Aging.Cold Spring Harbor perspectives in medicine · 2022
    Review
  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 at 1 institution in 1 country.

Simone Bersini *Molecular and Cell Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, United States.ORCID 0000-0003-4620-3500
Roberta Schulte *Molecular and Cell Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, United States.ORCID 0000-0003-3886-4800
Ling HuangThe Razavi Newman Integrative Genomics and Bioinformatics Core (IGC), The Salk Institute for Biological Studies, La Jolla, United States.
Hannah TsaiMolecular and Cell Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, United States.
Martin W HetzerMolecular and Cell Biology Laboratory, The Salk Institute for Biological Studies, La Jolla, United States.ORCID 0000-0002-2111-992X
Salk Institute for Biological Studies · US

Funding

Viral Vector Core (VVC)P30CA014195 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Reuben Shaw · 1985 to 2026
$82.8M
The role of long-lived proteins in the survival of nerve cellsR01NS096786 · NINDS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI HETZER, MARTIN W · 2015 to 2019
$3.6M
American Heart Association-Allen Initiative in Brain Health and Cognitive Impairment award 19PABH134610000NCI NIH HHS P30 014195NCI NIH HHS P30 CA014195NIH HHS R01 NS096786NINDS NIH HHS R01 NS096786
6 · The paper itself

Abstract

Vascular dysfunctions are a common feature of multiple age-related diseases. However, modeling healthy and pathological aging of the human vasculature represents an unresolved experimental challenge. Here, we generated induced vascular endothelial cells (iVECs) and smooth muscle cells (iSMCs) by direct reprogramming of healthy human fibroblasts from donors of different ages and Hutchinson-Gilford Progeria Syndrome (HGPS) patients. iVECs induced from old donors revealed upregulation of

Indexed as

AgingAnimalsEndothelial CellsGlutathione TransferaseHumansMiceMyocytes, Smooth MusclePhosphoprotein PhosphatasesProgeriaGlutathione TransferasePALD1 protein, humanPhosphoprotein Phosphatasesagingdirect reprogrammingendothelial cellhumanhutchinson-gilford progeria syndromemedicinemousesmooth muscle cellvascular barrier

Identifiers

PMID32896271
PMCPMC7478891
OpenAlexW3083391949

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.