Evidence map›Paper›PMID 33597582›Full record

ArticleScientific reports2021

Aortic carboxypeptidase-like protein regulates vascular adventitial progenitor and fibroblast differentiation through myocardin related transcription factor A.

Dahai Wang, Nabil Rabhi, Shaw-Fang Yet, Stephen R Farmer, Matthew D Layne

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

13 citing papers in PubMed, 13 citations in OpenAlex.

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  12. Aqueous extract ofFrontiers in pharmacology · 2023
    Article
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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

5 authors at 2 institutions in 2 countries.

Dahai WangDepartment of Biochemistry, Boston University School of Medicine, 72 E. Concord St, Boston, MA, 02118, USA.
Nabil RabhiDepartment of Biochemistry, Boston University School of Medicine, 72 E. Concord St, Boston, MA, 02118, USA.
Shaw-Fang YetInstitute of Cellular and System Medicine, National Health Research Institutes, Zhunan, 35053, Taiwan.
Stephen R FarmerDepartment of Biochemistry, Boston University School of Medicine, 72 E. Concord St, Boston, MA, 02118, USA.
Matthew D LayneDepartment of Biochemistry, Boston University School of Medicine, 72 E. Concord St, Boston, MA, 02118, USA. mlayne@bu.edu.
Boston University · USNational Health Research Institutes · TW

Funding

Role of ACLP in Vascular Smooth Muscle BiologyR01HL078869 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI LAYNE, MATTHEW D · 2007 to 2011
$2.2M
Healthy Remodeling of Obese Adipose TissueR01DK117161 · NIDDK · BOSTON UNIVERSITY MEDICAL CAMPUS · PI FARMER, STEPHEN ROBERT · 2018 to 2021
$1.9M
NHLBI NIH HHS R01 HL078869NIDDK NIH HHS R01 DK117161
6 · The paper itself

Abstract

The vascular adventitia contains numerous cell types including fibroblasts, adipocytes, inflammatory cells, and progenitors embedded within a complex extracellular matrix (ECM) network. In response to vascular injury, adventitial progenitors and fibroblasts become activated and exhibit increased proliferative capacity and differentiate into contractile cells that remodel the ECM. These processes can lead to vascular fibrosis and disease progression. Our previous work established that the ECM protein aortic carboxypeptidase-like protein (ACLP) promotes fibrotic remodeling in the lung and is activated by vascular injury. It is currently unknown what controls vascular adventitial cell differentiation and if ACLP has a role in this process. Using purified mouse aortic adventitia Sca1+ progenitors, ACLP repressed stem cell markers (CD34, KLF4) and upregulated smooth muscle actin (SMA) and collagen I expression. ACLP enhanced myocardin-related transcription factor A (MRTFA) activity in adventitial cells by promoting MRTFA nuclear translocation. Sca1 cells from MRTFA-null mice exhibited reduced SMA and collagen expression induced by ACLP, indicating Sca1 cell differentiation is regulated in part by the ACLP-MRTFA axis. We determined that ACLP induced vessel contraction and increased adventitial collagen in an explant model. Collectively these studies identified ACLP as a mediator of adventitial cellular differentiation, which may result in pathological vessel remodeling.

Indexed as

AdipocytesAdventitiaAnimalsAortaCarboxypeptidasesCell DifferentiationCollagen Type IFemaleFibroblastsMaleMiceMice, Inbred C57BLMice, KnockoutMuscle, Smooth, VascularMyocardinNuclear ProteinsAebp1 protein, mouseCarboxypeptidasesCollagen Type IMrtfa protein, mouseMyocardinNuclear ProteinsRepressor ProteinsTrans-ActivatorsTranscription Factors

Identifiers

PMID33597582
PMCPMC7889889
OpenAlexW3130667555

What OpenQuestion holds

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LicenceCC BY
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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.