Evidence map›Paper›PMID 31683735›Full record

ArticleCells2019

Mitotic Chromosomes in Live Cells Characterized Using High-Speed and Label-Free Optical Diffraction Tomography.

Tae-Keun Kim, Byong-Wook Lee, Fumihiko Fujii, Kee-Hang Lee, Sanghwa Lee, YongKeun Park, Jun Ki Kim, Sang-Wook Lee, Chan-Gi Pack

Open access · goldAbstract read
In one paragraph

Article in Cells, 2019. 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
2.9field-weighted citation impact, top 8% 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, 32 citations in OpenAlex.

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  7. The Enhancement of Antimicrobial Photodynamic Therapy ofInternational journal of molecular sciences · 2022
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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 3 institutions in 2 countries.

Tae-Keun KimAsan Institute for Life Sciences, Asan Medical Center, Seoul 05505, Korea. m996142@gmail.com.
Byong-Wook LeeAsan Institute for Life Sciences, Asan Medical Center, Seoul 05505, Korea. sorrow98@nate.com.
Fumihiko FujiiDivision of Physical Pharmacy, Faculty of Pharmaceutical Sciences, Kobe Gakuin University, Kobe 650-8586, Japan. ffujii4@gmail.com.
Kee-Hang LeeTomocube Inc., Daejeon 34051, Korea. khlee@tomocube.com.
Sanghwa LeeAsan Institute for Life Sciences, Asan Medical Center, Seoul 05505, Korea. pause1919@gmail.com.
YongKeun ParkTomocube Inc., Daejeon 34051, Korea. khlee@tomocube.com.
Jun Ki KimAsan Institute for Life Sciences, Asan Medical Center, Seoul 05505, Korea. kim@amc.seoul.kr.
Sang-Wook LeeDepartment of Radiation Oncology, University of Ulsan College of Medicine, Asan Medical Center, Seoul 05505, Korea. lsw@amc.seoul.kr.
Chan-Gi PackAsan Institute for Life Sciences, Asan Medical Center, Seoul 05505, Korea. changipack@amc.seoul.kr.
Ulsan College · KRAsan Medical Center · KRKobe Gakuin University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cell nucleus is a three-dimensional, dynamic organelle organized into subnuclear compartments such as chromatin and nucleoli. The structure and function of these compartments are maintained by diffusion and interactions between related factors as well as by dynamic and structural changes. Recent studies using fluorescent microscopic techniques suggest that protein factors can access and are freely mobile in heterochromatin and in mitotic chromosomes, despite their densely packed structure. However, the physicochemical properties of the chromosome during cell division are not fully understood. In the present study, characteristic properties such as the refractive index (RI), volume of the mitotic chromosomes, and diffusion coefficient (D) of fluorescent probes inside the chromosome were quantified using an approach combining label-free optical diffraction tomography with complementary confocal laser-scanning microscopy and fluorescence correlation spectroscopy. Variations in these parameters correlated with osmotic conditions, suggesting that changes in RI are consistent with those of the diffusion coefficient for mitotic chromosomes and cytosol. Serial RI tomography images of chromosomes in live cells during mitosis were compared with three-dimensional confocal micrographs to demonstrate that compaction and decompaction of chromosomes induced by osmotic change were characterized by linked changes in chromosome RI, volume, and the mobilities of fluorescent proteins.

Indexed as

MitosisAnimalsCell LineChromosomesCulture MediaCytosolMaleMicroscopy, ConfocalMuntjacsTomographyCulture Mediacellular viscositychromosomediffusion coefficientfluorescence correlation spectroscopymitosisoptical diffraction tomographyosmotic stressrefractive index

Identifiers

PMID31683735
PMCPMC6912651
OpenAlexW2982678631

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.