Evidence map›Paper›PMID 35859900›Full record

ArticleFrontiers in cell and developmental biology2022

Post-Transcriptional Dynamics is Involved in Rapid Adaptation to Hypergravity in Jurkat T Cells.

Christian Vahlensieck, Cora S Thiel, Daniel Pöschl, Timothy Bradley, Sonja Krammer, Beatrice Lauber, Jennifer Polzer, Oliver Ullrich

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 8 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

8 authors at 3 institutions in 3 countries.

Christian VahlensieckInstitute of Anatomy, Faculty of Medicine, University of Zurich, Zurich, Switzerland.
Cora S ThielInstitute of Anatomy, Faculty of Medicine, University of Zurich, Zurich, Switzerland.
Daniel PöschlInstitute of Anatomy, Faculty of Medicine, University of Zurich, Zurich, Switzerland.
Timothy BradleyInstitute of Anatomy, Faculty of Medicine, University of Zurich, Zurich, Switzerland.
Sonja KrammerInstitute of Anatomy, Faculty of Medicine, University of Zurich, Zurich, Switzerland.
Beatrice LauberInstitute of Anatomy, Faculty of Medicine, University of Zurich, Zurich, Switzerland.
Jennifer PolzerInstitute of Anatomy, Faculty of Medicine, University of Zurich, Zurich, Switzerland.
Oliver UllrichInstitute of Anatomy, Faculty of Medicine, University of Zurich, Zurich, Switzerland.
University of Zurich · CHErnst Abbe University of Applied Sciences Jena · DEKennedy Space Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transcriptome of human immune cells rapidly reacts to altered gravity in a highly dynamic way. We could show in previous experiments that transcriptional patterns show profound adaption after seconds to minutes of altered gravity. To gain further insight into these transcriptional alteration and adaption dynamics, we conducted a highly standardized RNA-Seq experiment with human Jurkat T cells exposed to 9xg hypergravity for 3 and 15 min, respectively. We investigated the frequency with which individual exons were used during transcription and discovered that differential exon usage broadly appeared after 3 min and became less pronounced after 15 min. Additionally, we observed a shift in the transcript pool from coding towards non-coding transcripts. Thus, adaption of gravity-sensitive differentially expressed genes followed a dynamic transcriptional rebound effect. The general dynamics were compatible with previous studies on the transcriptional effects of short hypergravity on human immune cells and suggest that initial up-regulatory changes mostly result from increased elongation rates. The shift correlated with a general downregulation of the affected genes. All chromosome bands carried homogenous numbers of gravity-sensitive genes but showed a specific tendency towards up- or downregulation. Altered gravity affected transcriptional regulation throughout the entire genome, whereby the direction of differential expression was strongly dependent on the structural location in the genome. A correlation analysis with potential mediators of the early transcriptional response identified a link between initially upregulated genes with certain transcription factors. Based on these findings, we have been able to further develop our model of the transcriptional response to altered gravity.

Indexed as

altered gravitygene expressiongravity-sensinghypergravityimmune cellsspace flight

Identifiers

PMID35859900
PMCPMC9289288
OpenAlexW4283790947

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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.