Evidence map›Paper›PMID 28066542›Full record

ArticleCell & bioscience2017

Characterization of tubular liquid crystal structure in embryonic stem cell derived embryoid bodies.

MengMeng Xu, Odell D Jones, Liyang Wang, Xin Zhou, Harry G Davis, Joseph L Bryant, Jianjie Ma, Willian B Isaacs, Xuehong Xu

Open access · goldAbstract read
In one paragraph

Article in Cell & bioscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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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

9 authors at 6 institutions in 2 countries.

MengMeng Xu *Department of Pharmacology, Duke University Medical Center, Durham, NC 27708 USA.
Odell D Jones *University of Pennsylvania ULAR, Philadelphia, PA 19144 USA.
Liyang Wang *The Laboratory of Cell Genetics and Developmental Biology (CGDB), Shaanxi Normal University College of Life Sciences, Xi'an, 710062 Shaanxi People's Republic of China.
Xin ZhouThe Laboratory of Cell Genetics and Developmental Biology (CGDB), Shaanxi Normal University College of Life Sciences, Xi'an, 710062 Shaanxi People's Republic of China.
Harry G DavisInstitute of Human Virology, University of Maryland School of Medicine, Baltimore, MD USA.
Joseph L BryantInstitute of Human Virology, University of Maryland School of Medicine, Baltimore, MD USA.
Jianjie MaOhio State University School of Medicine, Columbus, OH 43210 USA.
Willian B IsaacsJohns Hopkins School of Medicine, Baltimore, MD 21287 USA.
Xuehong XuThe Laboratory of Cell Genetics and Developmental Biology (CGDB), Shaanxi Normal University College of Life Sciences, Xi'an, 710062 Shaanxi People's Republic of China.ORCID 0000-0003-2986-1771
Shaanxi Normal University · CNUniversity of Maryland, Baltimore · USDuke University · USJohns Hopkins University · USThe Ohio State University · USUniversity of Pennsylvania · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007171 · NIGMS · DUKE UNIVERSITY · PI KONTOS, CHRISTOPHER D · 1985 to 2021
$31.2M
Medical Scientist Training Program Training GrantT32GM145449 · NIGMS · DUKE UNIVERSITY · PI Christopher D Kontos · 2022 to 2026
$6.6M
NIGMS NIH HHS T32 GM007171NIGMS NIH HHS T32 GM145449
6 · The paper itself

Abstract

backgroundMassive liquid crystal droplets have been found during embryonic development in more than twenty different tissues and organs, including the liver, brain and kidney. Liquid crystal deposits have also been identified in multiple human pathologies, including vascular disease, liver dysfunction, age-related macular degeneration, and other chronic illnesses. Despite the involvement of liquid crystals in such a large number of human processes, this phenomenon is poorly understood and there are no in vitro systems to further examine the function of liquid crystals in biology.

resultsWe report the presence of tubular birefringent structures in embryoid bodies (EBs) differentiated in culture. These birefringent tubular structures initiate at the EB surface and penetrated the cortex at a variety of depths. Under crossed polarized light, these tubules are seen as a collection of birefringent Maltese crosses and tubules with birefringent walls and a non-birefringent lumen. The fluidity of these birefringent structures under pressure application led to elongation and widening, which was partially recoverable with pressure release. These birefringent structures also displayed heat triggered phase transition from liquid crystal to isotropic status that is partially recoverable with return to ambient temperature. These pressure and temperature triggered changes confirm the birefringent structures as liquid crystals. The first report of liquid crystal so early in development.

conclusionThe structure of the liquid crystal tubule network we observed distributed throughout the differentiated embryoid bodies may function as a transportation network for nutrients and metabolic waste during EB growth, and act as a precursor to the vascular system. This observation not only reveals the involvement of liquid crystals earlier than previously known, but also provides a method for studying liquid crystals in vitro.

Indexed as

Embryoid bodyEmbryonic stem cellLiquid crystalPhase transition

Identifiers

PMID28066542
PMCPMC5210172
OpenAlexW2561454806

What OpenQuestion holds

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LicenceCC BY
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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.