Evidence map›Paper›PMID 38825882›Full record

ArticleAging cell2024

Mapping the unicellular transcriptome of the ascending thoracic aorta to changes in mechanosensing and mechanoadaptation during aging.

Cristobal F Rivera, Yasmeen M Farra, Michele Silvestro, Steven Medvedovsky, Jacqueline Matz, Muhammad Yogi Pratama, John Vlahos, Bhama Ramkhelawon, Chiara Bellini

Abstract read
In one paragraph

Article in Aging cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Growth arrest of thoracic aortic aneurysms in aging Marfan mice.American journal of physiology. Heart and circulatory physiology · 2026
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  2. Review
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  11. TheFrontiers in cardiovascular medicine · 2024
    Article
  12. Review
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

9 authors.

Cristobal F RiveraDepartment of Surgery, Division of Vascular and Endovascular Surgery, New York University Langone Medical Center, New York, New York, USA.ORCID 0000-0001-9648-9880
Yasmeen M FarraDepartment of Bioengineering, Northeastern University, Boston, Massachusetts, USA.
Michele SilvestroDepartment of Surgery, Division of Vascular and Endovascular Surgery, New York University Langone Medical Center, New York, New York, USA.
Steven MedvedovskyDepartment of Surgery, Division of Vascular and Endovascular Surgery, New York University Langone Medical Center, New York, New York, USA.ORCID 0009-0008-9727-5698
Jacqueline MatzDepartment of Bioengineering, Northeastern University, Boston, Massachusetts, USA.
Muhammad Yogi PratamaDepartment of Surgery, Division of Vascular and Endovascular Surgery, New York University Langone Medical Center, New York, New York, USA.
John VlahosDepartment of Surgery, Division of Vascular and Endovascular Surgery, New York University Langone Medical Center, New York, New York, USA.
Bhama RamkhelawonDepartment of Surgery, Division of Vascular and Endovascular Surgery, New York University Langone Medical Center, New York, New York, USA.ORCID 0000-0002-9087-0995
Chiara BelliniDepartment of Bioengineering, Northeastern University, Boston, Massachusetts, USA.ORCID 0000-0003-0823-4613

Funding

Spatiotemporal checkpoints of macrophages in aortic aneurysms- RenewalR01HL146627 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Bhama Ramkhelawon · 2019 to 2026
$6.1M
Cardiopulmonary outcomes of dual cigarette and e-cigarette use in animal models of chronic exposureR01HL168719 · NHLBI · NORTHEASTERN UNIVERSITY · PI Chiara Bellini · 2023 to 2026
$3.1M
Origin and Immune Functions of Platelets in Aortic AneurysmsR01HL149927 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI RAMKHELAWON, BHAMA · 2020 to 2023
$2.4M
Evaluation of aortic stiffening as an early indicator of anthracycline-induced cardiotoxicityR21HL148747 · NHLBI · NORTHEASTERN UNIVERSITY · PI BELLINI, CHIARA · 2019 to 2020
$433k
American Heart Association 23PRE1023003American Heart Association 907602National Institute of Health R01HL146627National Institute of Health R01HL149927National Institute of Health R01HL168719National Institute of Health R21HL148747National Science Foundation GRFP1451070NHLBI NIH HHS R01 HL146627NHLBI NIH HHS R01 HL149927NHLBI NIH HHS R01 HL168719NHLBI NIH HHS R21 HL148747
6 · The paper itself

Abstract

Aortic stiffening is an inevitable manifestation of chronological aging, yet the mechano-molecular programs that orchestrate region- and layer-specific adaptations along the length and through the wall of the aorta are incompletely defined. Here, we show that the decline in passive cyclic distensibility is more pronounced in the ascending thoracic aorta (ATA) compared to distal segments of the aorta and that collagen content increases in both the medial and adventitial compartments of the ATA during aging. The single-cell RNA sequencing of aged ATA tissues reveals altered cellular senescence, remodeling, and inflammatory responses accompanied by enrichment of T-lymphocytes and rarefaction of vascular smooth muscle cells, compared to young samples. T lymphocyte clusters accumulate in the adventitia, while the activation of mechanosensitive Piezo-1 enhances vasoconstriction and contributes to the overall functional decline of ATA tissues. These results portray the immuno-mechanical aging of the ATA as a process that culminates in a stiffer conduit permissive to the accrual of multi-gerogenic signals priming to disease development.

Indexed as

AgingAorta, ThoracicTranscriptomeAnimalsHumansMaleMechanotransduction, Cellularcollagen remodelingdistensibilityelastic energyinflammationPiezo‐1tissue stiffnessvasoconstriction

Identifiers

PMID38825882
PMCPMC11320362

What OpenQuestion holds

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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.