Evidence map›Paper›PMID 37564277›Full record

ArticleAPL bioengineering2023

Direct differentiation of human pluripotent stem cells into vascular network along with supporting mural cells.

Taylor Bertucci, Shravani Kakarla, Max A Winkelman, Keith Lane, Katherine Stevens, Steven Lotz, Alexander Grath, Daylon James, Sally Temple, Guohao Dai

Open access · goldAbstract read
In one paragraph

Article in APL bioengineering, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

10 authors at 3 institutions in 1 country.

Taylor BertucciNeural Stem Cell Institute, Rensselaer, New York 12144, USA.ORCID https://orcid.org/0009-0008-1017-6807
Shravani KakarlaNortheastern University, Department of Bioengineering, Boston, Massachusetts 02115, USA.ORCID https://orcid.org/0009-0005-7353-4518
Max A WinkelmanNortheastern University, Department of Bioengineering, Boston, Massachusetts 02115, USA.ORCID https://orcid.org/0000-0003-2252-8212
Keith LaneNeural Stem Cell Institute, Rensselaer, New York 12144, USA.
Katherine StevensNeural Stem Cell Institute, Rensselaer, New York 12144, USA.ORCID https://orcid.org/0009-0004-2388-0722
Steven LotzNeural Stem Cell Institute, Rensselaer, New York 12144, USA.
Alexander GrathNortheastern University, Department of Bioengineering, Boston, Massachusetts 02115, USA.ORCID https://orcid.org/0000-0003-2812-1384
Daylon JamesWeill Cornell Medicine, New York, New York 10065, USA.
Sally TempleNeural Stem Cell Institute, Rensselaer, New York 12144, USA.ORCID https://orcid.org/0000-0001-7301-783X
Guohao DaiNortheastern University, Department of Bioengineering, Boston, Massachusetts 02115, USA.ORCID https://orcid.org/0000-0001-7346-2685
Neural Stem Cell Institute · USNortheastern University · USCornell University · US

Funding

Investigating the Functional Impact of AD Risk Genes on Neuro-Vascular InteractionsU01AG072464 · NIA · REGENERATIVE RESEARCH FOUNDATION · PI HARARI, OSCAR, KAMPMANN, MARTIN · 2021 to 2025
$8.7M
Role of endothelial Sox17 in EC-SMC crosstalk and homeostatic regulation of blood vessel adaption to arterial hemodynamicsR01HL162908 · NHLBI · NORTHEASTERN UNIVERSITY · PI DAI, GUOHAO, DARDIK, ALAN · 2022 to 2025
$2.3M
Differentiating Embryonic Stem Cells Toward Arterial and Venous Endothelial Cells For Vascular RegenerationR01HL118245 · NHLBI · RENSSELAER POLYTECHNIC INSTITUTE · PI DAI, GUOHAO · 2013 to 2017
$1.9M
American Heart Association-American Stroke Association 19IPLOI34760604NHLBI NIH HHS R01 HL118245NHLBI NIH HHS R01 HL162908NIA NIH HHS U01 AG072464
6 · The paper itself

Abstract

During embryonic development, endothelial cells (ECs) undergo vasculogenesis to form a primitive plexus and assemble into networks comprised of mural cell-stabilized vessels with molecularly distinct artery and vein signatures. This organized vasculature is established prior to the initiation of blood flow and depends on a sequence of complex signaling events elucidated primarily in animal models, but less studied and understood in humans. Here, we have developed a simple vascular differentiation protocol for human pluripotent stem cells that generates ECs, pericytes, and smooth muscle cells simultaneously. When this protocol is applied in a 3D hydrogel, we demonstrate that it recapitulates the dynamic processes of early human vessel formation, including acquisition of distinct arterial and venous fates, resulting in a vasculogenesis angiogenesis model plexus (VAMP). The VAMP captures the major stages of vasculogenesis, angiogenesis, and vascular network formation and is a simple, rapid, scalable model system for studying early human vascular development

Identifiers

PMID37564277
PMCPMC10411996
OpenAlexW4385752057

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.