Evidence map›Paper›PMID 38517229›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2024

A cell atlas of thoracic aortic perivascular adipose tissue: a focus on mechanotransducers.

Janice M Thompson, Stephanie W Watts, Leah Terrian, G Andres Contreras, Cheryl Rockwell, C Javier Rendon, Emma Wabel, Lizbeth Lockwood, Sudin Bhattacharya, Rance Nault

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 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
5.2field-weighted citation impact, top 4% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Mechanotransduction in the Perivascular Adipose Tissue.Arteriosclerosis, thrombosis, and vascular biology · 2025
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Janice M ThompsonDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan, United States.ORCID 0000-0002-1669-409X
Stephanie W WattsDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan, United States.ORCID 0000-0002-9653-6357
Leah TerrianDepartment of Biomedical Engineering, Michigan State University, East Lansing, Michigan, United States.
G Andres ContrerasDepartment of Large Animal Clinical Sciences, Michigan State University, East Lansing, Michigan, United States.ORCID 0000-0003-4969-2178
Cheryl RockwellDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan, United States.ORCID 0000-0002-0987-3460
C Javier RendonDepartment of Large Animal Clinical Sciences, Michigan State University, East Lansing, Michigan, United States.ORCID 0000-0002-1439-777X
Emma WabelDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan, United States.ORCID 0000-0002-5820-5645
Lizbeth LockwoodDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan, United States.
Sudin BhattacharyaDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan, United States.ORCID 0000-0002-2360-1672
Rance NaultDepartment of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan, United States.ORCID 0000-0002-6822-4962
Michigan United · US

Funding

The perivascular adipocyte: integrating mechanical and structural cues into vasoactive functionP01HL152951 · NHLBI · MICHIGAN STATE UNIVERSITY · PI Stephanie W Watts · 2022 to 2026
$13.3M
Integrative Pharmacological Sciences Training Program (IPSTP)T32GM142521 · NIGMS · MICHIGAN STATE UNIVERSITY · PI ANNE M. DORRANCE, Gina Marie Leinninger · 2021 to 2026
$2.4M
HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) P01HL152951HHS | NIH | National Institute of General Medical Sciences (NIGMS) T32GM142521NHLBI NIH HHS P01 HL152951NIGMS NIH HHS T32 GM142521
6 · The paper itself

Abstract

Perivascular adipose tissue (PVAT) is increasingly recognized for its function in mechanotransduction. However, major gaps remain in our understanding of the cells present in PVAT, as well as how different cells contribute to mechanotransduction. We hypothesized that snRNA-seq would reveal the expression of mechanotransducers, and test one (PIEZO1) to illustrate the expression and functional agreement between single-nuclei RNA sequencing (snRNA-seq) and physiological measurements. To contrast two brown tissues, subscapular brown adipose tissue (BAT) was also examined. We used snRNA-seq of the thoracic aorta PVAT (taPVAT) and BAT from male Dahl salt-sensitive (Dahl SS) rats to investigate cell-specific expression mechanotransducers. Localization and function of the mechanostransducer PIEZO1 were further examined using immunohistochemistry (IHC) and RNAscope, as well as pharmacological antagonism. Approximately 30,000 nuclei from taPVAT and BAT each were characterized by snRNA-seq, identifying eight major cell types expected and one unexpected (nuclei with oligodendrocyte marker genes). Cell-specific differential gene expression analysis between taPVAT and BAT identified up to 511 genes (adipocytes) with many (≥20%) being unique to individual cell types.

Indexed as

Adipose Tissue, BrownAorta, ThoracicIon ChannelsMechanotransduction, CellularMembrane ProteinsRats, Inbred DahlAdipose TissueAnimalsHypertensionMaleRatsRNA-SeqIon ChannelsMembrane ProteinsPiezo1 protein, ratbrown adipose tissueDahl-SS ratmechanotransductionperivascular adipose tissuePiezo1

Identifiers

PMID38517229
PMCPMC11380965
OpenAlexW4393070059

What OpenQuestion holds

Textmetadata
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.