Evidence map›Paper›PMID 37016052›Full record

ArticleScientific reports2023

Parallel recovery of chromatin accessibility and gene expression dynamics from frozen human regulatory T cells.

Ying Y Wong, Jessica E Harbison, Christopher M Hope, Batjargal Gundsambuu, Katherine A Brown, Soon W Wong, Cheryl Y Brown, Jennifer J Couper, Jimmy Breen, Ning Liu and 7 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

11 citing papers in PubMed, 41 citations in OpenAlex.

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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

17 authors at 4 institutions in 2 countries.

Ying Y WongRobinson Research Institute, University of Adelaide, Adelaide, Australia.
Jessica E HarbisonRobinson Research Institute, University of Adelaide, Adelaide, Australia.
Christopher M HopeRobinson Research Institute, University of Adelaide, Adelaide, Australia.
Batjargal GundsambuuRobinson Research Institute, University of Adelaide, Adelaide, Australia.
Katherine A BrownRobinson Research Institute, University of Adelaide, Adelaide, Australia.
Soon W WongRobinson Research Institute, University of Adelaide, Adelaide, Australia.
Cheryl Y BrownRobinson Research Institute, University of Adelaide, Adelaide, Australia.
Jennifer J CouperRobinson Research Institute, University of Adelaide, Adelaide, Australia.
Jimmy BreenRobinson Research Institute, University of Adelaide, Adelaide, Australia.
Ning LiuRobinson Research Institute, University of Adelaide, Adelaide, Australia.
Stephen M PedersonRobinson Research Institute, University of Adelaide, Adelaide, Australia.
Maren KöhneGerman Center for Neurodegenerative Diseases, University of Bonn, Bonn, Germany.
Kathrin KleeGerman Center for Neurodegenerative Diseases, University of Bonn, Bonn, Germany.
Joachim SchultzeGerman Center for Neurodegenerative Diseases, University of Bonn, Bonn, Germany.
Marc BeyerGerman Center for Neurodegenerative Diseases, University of Bonn, Bonn, Germany.
Timothy SadlonRobinson Research Institute, University of Adelaide, Adelaide, Australia.
Simon C BarryRobinson Research Institute, University of Adelaide, Adelaide, Australia. simon.barry@adelaide.edu.au.
University of Adelaide · AUWomen's and Children's Hospital · AUGerman Center for Neurodegenerative Diseases · DEUniversity of Bonn · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epigenetic features such as DNA accessibility dictate transcriptional regulation in a cell type- and cell state- specific manner, and mapping this in health vs. disease in clinically relevant material is opening the door to new mechanistic insights and new targets for therapy. Assay for Transposase Accessible Chromatin Sequencing (ATAC-seq) allows chromatin accessibility profiling from low cell input, making it tractable on rare cell populations, such as regulatory T (Treg) cells. However, little is known about the compatibility of the assay with cryopreserved rare cell populations. Here we demonstrate the robustness of an ATAC-seq protocol comparing primary Treg cells recovered from fresh or cryopreserved PBMC samples, in the steady state and in response to stimulation. We extend this method to explore the feasibility of conducting simultaneous quantitation of chromatin accessibility and transcriptome from a single aliquot of 50,000 cryopreserved Treg cells. Profiling of chromatin accessibility and gene expression in parallel within the same pool of cells controls for cellular heterogeneity and is particularly beneficial when constrained by limited input material. Overall, we observed a high correlation of accessibility patterns and transcription factor dynamics between fresh and cryopreserved samples. Furthermore, highly similar transcriptomic profiles were obtained from whole cells and from the supernatants recovered from ATAC-seq reactions. We highlight the feasibility of applying these techniques to profile the epigenomic landscape of cells recovered from cryopreservation biorepositories.

Indexed as

ChromatinT-Lymphocytes, RegulatoryHigh-Throughput Nucleotide SequencingHumansLeukocytes, MononuclearTranscriptomeChromatin

Identifiers

PMID37016052
PMCPMC10073253
OpenAlexW4362595446

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.