Evidence map›Paper›PMID 37577183›Full record

ArticleAdvanced therapeutics2023

Engineered Vasculogenic Extracellular Vesicles Drive Nonviral Direct Conversions of Human Dermal Fibroblasts into Induced Endothelial Cells and Improve Wound Closure.

Maria A Rincon-Benavides, Natalia Claire Mendonca, Tatiana Z Cuellar-Gaviria, Ana I Salazar-Puerta, Lilibeth Ortega-Pineda, Britani N Blackstone, Binbin Deng, David W McComb, Daniel Gallego-Perez, Heather M Powell and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Advanced therapeutics, 2023. 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
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

19 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Isolation of Extracellular Vesicles From Mouse Brown Adipose Tissue Secretome Using Size-Exclusion Chromatography.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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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 1 institution in 1 country.

Maria A Rincon-BenavidesBiophysics Graduate Program, The Ohio State University, Columbus, OH.
Natalia Claire MendoncaDepartment of Biomedical Engineering, The Ohio State University, Columbus, OH.
Tatiana Z Cuellar-GaviriaDepartment of Biomedical Engineering, The Ohio State University, Columbus, OH.
Ana I Salazar-PuertaDepartment of Biomedical Engineering, The Ohio State University, Columbus, OH.
Lilibeth Ortega-PinedaDepartment of Biomedical Engineering, The Ohio State University, Columbus, OH.
Britani N BlackstoneDepartment of Materials Science and Engineering, The Ohio State University, Columbus, OH.
Binbin DengCenter for Electron Microscopy and Analysis (CEMAS), The Ohio State University, Columbus, OH.
David W McCombDepartment of Materials Science and Engineering, The Ohio State University, Columbus, OH.
Daniel Gallego-PerezBiophysics Graduate Program, The Ohio State University, Columbus, OH.
Heather M PowellBiophysics Graduate Program, The Ohio State University, Columbus, OH.
Natalia Higuita-CastroBiophysics Graduate Program, The Ohio State University, Columbus, OH.
The Ohio State University · US

Funding

Novel nanoscale approaches to whole tissue reprogrammingDP2EB028110 · NIBIB · OHIO STATE UNIVERSITY · PI GALLEGO-PEREZ, DANIEL · 2018 to 2022
$2.7M
Novel non-viral reprogramming strategies to treat Discogenic back pain via engineered extracellular vesiclesR01AR079485 · NIAMS · OHIO STATE UNIVERSITY · PI Natalia Higuita-Castro, Devina Purmessur (Walter) · 2022 to 2026
$2.5M
Non-Viral Modulation of Cutaneous Tissue Plasticity as a Therapy for DiabetesDP1DK126199 · NIDDK · OHIO STATE UNIVERSITY · PI GALLEGO-PEREZ, DANIEL · 2020 to 2020
$737k
NIAMS NIH HHS R01 AR079485NIBIB NIH HHS DP2 EB028110NIDDK NIH HHS DP1 DK126199
6 · The paper itself

Abstract

Vasculogenic cell therapies have emerged as a powerful tool to increase vascularization and promote tissue repair/regeneration. Current approaches to cell therapies, however, rely mostly on progenitor cells, which pose significant risks (e.g., uncontrolled differentiation, tumorigenesis, and genetic/epigenetic abnormalities). Moreover, reprogramming methodologies used to generate induced endothelial cells (iECs) from induced pluripotent stem cells rely heavily on viral vectors, which pose additional translational limitations. This work describes the development of engineered human extracellular vesicles (EVs) capable of driving reprogramming-based vasculogenic therapies without the need for progenitor cells and/or viral vectors. The EVs were derived from primary human dermal fibroblasts (HDFs), and were engineered to pack transcription factor genes/transcripts of

Indexed as

engineered EVsinduced endotheliumischemic disordersvasculogenic therapies

Identifiers

PMID37577183
PMCPMC10416766
OpenAlexW4313456952

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.