Evidence map›Paper›PMID 36112115›Full record

ArticleAdvanced healthcare materials2022

Monocyte Recruitment for Vascular Tissue Regeneration.

Bita Nasiri, Tai Yi, Yulun Wu, Randall J Smith, Ashis Kumar Podder, Christopher K Breuer, Stelios T Andreadis

Open access · greenAbstract read
In one paragraph

Article in Advanced healthcare materials, 2022. 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
1.1field-weighted citation impact, top 26% 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, 16 citations in OpenAlex.

  1. Article
  2. From inflammation to remodelling: A novel BASP1Journal of advanced research · 2025
    Article
  3. Article
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  7. Review
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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

7 authors at 2 institutions in 1 country.

Bita NasiriDepartment of Chemical and Biological Engineering, University at Buffalo, The State University of New York, Amherst, NY, 14260-4200, USA.
Tai YiNationwide Children's Hospital, Columbus, OH, 43215, USA.
Yulun WuDepartment of Chemical and Biological Engineering, University at Buffalo, The State University of New York, Amherst, NY, 14260-4200, USA.
Randall J SmithDepartment of Biomedical Engineering, University at Buffalo, The State University of New York, Amherst, NY, 14260-4200, USA.
Ashis Kumar PodderDepartment of Chemical and Biological Engineering, University at Buffalo, The State University of New York, Amherst, NY, 14260-4200, USA.
Christopher K BreuerNationwide Children's Hospital, Columbus, OH, 43215, USA.
Stelios T AndreadisDepartment of Chemical and Biological Engineering, University at Buffalo, The State University of New York, Amherst, NY, 14260-4200, USA.ORCID 0000-0001-9885-0457
University at Buffalo, State University of New York · USNationwide Children's Hospital · US

Funding

Cell-free vascular grafts: immunological response and vascular regenerationR01HL151196 · NHLBI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI ANDREADIS, STELIOS THEOHARIS · 2020 to 2023
$2.4M
NHLBI NIH HHS R01 HL151196
6 · The paper itself

Abstract

A strategy to recruit monocytes (MCs) from blood to regenerate vascular tissue from unseeded (cell-free) tissue engineered vascular grafts is presented. When immobilized on the surface of vascular grafts, the fusion protein, H2R5 can capture blood-derived MC under static or flow conditions in a shear stress dependent manner. The bound MC turns into macrophages (Mϕ) expressing both M1 and M2 phenotype specific genes. When H2R5 functionalized acellular-tissue engineered vessels (A-TEVs) are implanted into the mouse aorta, they remain patent and form a continuous endothelium expressing both endothelial cell (EC) and MC specific proteins. Underneath the EC layer, multiple cells layers are formed coexpressing both smooth muscle cell (SMC) and MC specific markers. Lineage tracing analysis using a novel CX3CR1-confetti mouse model demonstrates that fluorescently labeled MC populates the graft lumen by two and four weeks postimplantation, providing direct evidence in support of MC/Mϕ recruitment to the graft lumen. Given their abundance in the blood, circulating MCs may be a great source of cells that contribute directly to the endothelialization and vascular wall formation of acellular vascular grafts under the right chemical and biomechanical cues.

Indexed as

MonocytesTissue EngineeringAnimalsBlood Vessel ProsthesisEndothelial CellsEndothelium, VascularMiceMyocytes, Smooth Muscleendothelializationimmunoengineeringmacrophagesmonocytesvascular grafts

Identifiers

PMID36112115
PMCPMC9671850
OpenAlexW4296037363

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.