Evidence map›Paper›PMID 30247461›Full record

ArticleJournal of visualized experiments : JoVE2018

Fabrication of a Multiplexed Artificial Cellular MicroEnvironment Array.

Yasumasa Mashimo, Momoko Yoshioka, Yumie Tokunaga, Christopher Fockenberg, Shiho Terada, Yoshie Koyama, Teiko Shibata-Seki, Koki Yoshimoto, Risako Sakai, Hayase Hakariya and 7 more

Open access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 54% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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 3 countries.

Yasumasa MashimoInstitute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University; Department of Life Science and Technology, School of Life Science and Technology, Tokyo Institute of Technology.
Momoko YoshiokaInstitute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University.
Yumie TokunagaInstitute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University.
Christopher FockenbergInstitute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University.
Shiho TeradaInstitute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University.
Yoshie KoyamaInstitute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University.
Teiko Shibata-SekiDepartment of Life Science and Technology, School of Life Science and Technology, Tokyo Institute of Technology.
Koki YoshimotoInstitute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University.
Risako SakaiInstitute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University.
Hayase HakariyaInstitute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University.
Li LiuInstitute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University.
Toshihiro AkaikeBiomaterials Center for Regenerative Medical Engineering, Foundation for Advancement of International Science.
Eiry KobatakeDepartment of Life Science and Technology, School of Life Science and Technology, Tokyo Institute of Technology.
Siew-Eng HowFaculty of Science and Natural Resources, Universiti Malaysia Sabah.
Motonari UesugiInstitute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University; Institute for Chemical Research, Kyoto University.
Yong ChenInstitute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University; Ecole Normale Supérieure.
Ken-Ichiro KameiInstitute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University; kkamei@icems.kyoto-u.ac.jp.
Kyoto University · JPMaterial Sciences (United States) · USTokyo Institute of Technology · JPUniversiti of Malaysia Sabah · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cellular microenvironments consist of a variety of cues, such as growth factors, extracellular matrices, and intercellular interactions. These cues are well orchestrated and are crucial in regulating cell functions in a living system. Although a number of researchers have attempted to investigate the correlation between environmental factors and desired cellular functions, much remains unknown. This is largely due to the lack of a proper methodology to mimic such environmental cues in vitro, and simultaneously test different environmental cues on cells. Here, we report an integrated platform of microfluidic channels and a nanofiber array, followed by high-content single-cell analysis, to examine stem cell phenotypes altered by distinct environmental factors. To demonstrate the application of this platform, this study focuses on the phenotypes of self-renewing human pluripotent stem cells (hPSCs). Here, we present the preparation procedures for a nanofiber array and the microfluidic structure in the fabrication of a Multiplexed Artificial Cellular MicroEnvironment (MACME) array. Moreover, overall steps of the single-cell profiling, cell staining with multiple fluorescent markers, multiple fluorescence imaging, and statistical analyses, are described.

Indexed as

Cell DifferentiationCellular MicroenvironmentHumans

Identifiers

PMID30247461
PMCPMC6235102
OpenAlexW2890624620

What OpenQuestion holds

Textmetadata
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.