Evidence map›Paper›PMID 39006461›Full record

ArticleBiology methods & protocols2024

Two methods of isolation of rat aortic smooth muscle cells with high yield.

Saran Lotfollahzadeh, Asha Jose, Esha Zarnaab Shafiq, Nourhan El Sherif, Michael Smith, Jingyan Han, Francesca Seta, Vipul Chitalia

Abstract read
In one paragraph

Article in Biology methods & protocols, 2024. 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
–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

2 citing papers in PubMed.

  1. Review
  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

8 authors.

Saran LotfollahzadehRenal Section, Department of Medicine, Chobanian & Avedisian School of Medicine, Boston University, Boston, MA 02118, United States.
Asha JoseRenal Section, Department of Medicine, Chobanian & Avedisian School of Medicine, Boston University, Boston, MA 02118, United States.
Esha Zarnaab ShafiqRenal Section, Department of Medicine, Chobanian & Avedisian School of Medicine, Boston University, Boston, MA 02118, United States.
Nourhan El SherifDepartment of Biomedical Engineering, College of Engineering, Boston University, Boston, MA 02118, United States.
Michael SmithDepartment of Biomedical Engineering, College of Engineering, Boston University, Boston, MA 02118, United States.
Jingyan HanWhitaker Cardiovascular Institute, Department of Medicine, Vascular Biology Section, Chobanian & Avedisian School of Medicine, Boston University, Boston, MA 02118, United States.
Francesca SetaWhitaker Cardiovascular Institute, Department of Medicine, Vascular Biology Section, Chobanian & Avedisian School of Medicine, Boston University, Boston, MA 02118, United States.
Vipul ChitaliaRenal Section, Department of Medicine, Chobanian & Avedisian School of Medicine, Boston University, Boston, MA 02118, United States.ORCID https://orcid.org/0000-0002-6663-6058

Funding

Multidisciplinary Training Program in Cardiovascular EpidemiologyT32HL125232 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI Matthew G. Nayor, Vanessa Xanthakis · 2016 to 2026
$5.0M
Disease-specific risk factors for thrombosis following vascular interventionsR01HL166608 · NHLBI · BOSTON MEDICAL CENTER · PI Vipul C Chitalia, KATYA RAVID · 2023 to 2026
$2.7M
Role of intravascular ultrasound in Central Venous Stenosis in ESRD patientsR21DK119740 · NIDDK · BOSTON MEDICAL CENTER · PI CHITALIA, VIPUL C · 2020 to 2021
$503k
Frequency domain shortwave infrared spectroscopy (FD-SWIRS) for volume status monitoring during hemodialysis in end stage kidney diseaseR21DK132784 · NIDDK · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI CHITALIA, VIPUL C, ROBLYER, DARREN MICHAEL · 2022 to 2023
$478k
NHLBI NIH HHS R01 HL166608NHLBI NIH HHS T32 HL125232NIDDK NIH HHS R21 DK119740NIDDK NIH HHS R21 DK132784
6 · The paper itself

Abstract

Vascular smooth muscle cells (VSMCs) are an integral part of blood vessels and are the focus of intensive research in vascular biology, translational research, and cardiovascular diseases. Though immortalized vascular smooth muscle cell lines are available, their use is limited, underscoring the need for primary VSMCs. There are several methods for isolating primary cells from mice. However, the isolation method from rat blood vessels requires optimization, given the differences in the aorta of mice and rats. Here we compare two methods for VSMCs isolation from rats: enzymatic digestion and the "block" method. We observed a significantly higher yield of VSMCs using the enzymatic digestion method. We further confirmed that VSMCs expressed well-established VSMC-specific markers (calponin) with both methods and observed the persistence of this marker up to 9 passages, suggesting a continuation of the secretory phenotype of VSMCs. Overall, this work compares two methods and demonstrates a practical and effective method for isolating VSMCs from rat aorta, providing vascular biologists with a valuable and reliable experimental tool.

Indexed as

cardiovascular diseasecell markerscell survivalthrombosisvascular smooth muscle cells

Identifiers

PMID39006461
PMCPMC11244693

What OpenQuestion holds

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Registered trials

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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.