Evidence map›Paper›PMID 30145679›Full record

ArticleIn vitro cellular & developmental biology. Animal2018

A basic study on self-reconstitution of alveolar epithelium-like cells by tissue stem cells in mouse lung.

Masamichi Hayashi, Naoki Yamamoto, Noriko Hiramatsu, Sumito Isogai, Yusuke Gotoh, Yasuhiro Goto, Masashi Kondo, Kazuyoshi Imaizumi

Abstract read
PubMed Publisher
In one paragraph

Article in In vitro cellular & developmental biology. Animal, 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
0.5field-weighted citation impact, top 32% 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, 3 citations in OpenAlex.

  1. Article
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 1 institution in 1 country.

Masamichi HayashiDepartment of Respiratory Medicine, School of Medicine, Fujita Health University, Toyoake, Aichi, 470-1192, Japan.
Naoki YamamotoRegenerative Medicine Support Promotion Facility, Center for Research Promotion and Support, Fujita Health University, Toyoake, Aichi, 470-1192, Japan. naokiy@fujita-hu.ac.jp.ORCID http://orcid.org/0000-0002-9659-3204
Noriko HiramatsuDepartment of Respiratory Medicine, School of Medicine, Fujita Health University, Toyoake, Aichi, 470-1192, Japan.
Sumito IsogaiDepartment of Respiratory Medicine, School of Medicine, Fujita Health University, Toyoake, Aichi, 470-1192, Japan.
Yusuke GotohDepartment of Respiratory Medicine, School of Medicine, Fujita Health University, Toyoake, Aichi, 470-1192, Japan.
Yasuhiro GotoDepartment of Respiratory Medicine, School of Medicine, Fujita Health University, Toyoake, Aichi, 470-1192, Japan.
Masashi KondoDepartment of Respiratory Medicine, School of Medicine, Fujita Health University, Toyoake, Aichi, 470-1192, Japan.
Kazuyoshi ImaizumiDepartment of Respiratory Medicine, School of Medicine, Fujita Health University, Toyoake, Aichi, 470-1192, Japan.
Fujita Health University · JP

Funding

Japan Agency for Medical Research and Development 17mk0101051h0102Japan Agency for Medical Research and Development (JP) JP17ek0410040JSPS KAKENHI JP17K09677JSPS KAKENHI JP17K11495
6 · The paper itself

Abstract

In recent research on regenerative medicine, three-dimensional (3D) tissue reconstruction using the induced pluripotent stem cell (iPS cell) differentiated cells has attracted attention. In this study, mouse lungs at 1.5, 10, and 20 d old were subjected to enzyme treatment, and aggregates formed in serum-free suspension culture (3D-culture) were observed. The number of aggregates formed was the highest in 1.5 d. The cell aggregates in which the interior of the aggregate is filled and form small vacuoles and the organoid-like aggregates having a relatively large vacuole inside and forming the alveolar-like structure were observed. At 1.5 d, the formation ratio of the organoid-like aggregates was the highest and aggregate size was small at 20 d. For the cell aggregates derived from 1.5 d, positive cells of SSEA-1, CD29, CD90, CD105, alveolar epithelial stem cell marker of SP-C, and Sca-1 were observed in the center. In the cell aggregates derived from 10 d, the expression level of 1.5 d each protein markers and OCT4 gene of transcription factor was decreased, and furthermore, markers were hardly observed in the organoid-like aggregates derived from 10 d. In addition, cells surrounding the vacuole of organoid-like aggregate obtained over 10 d differentiated into periodic acid-Schiff (PAS), podoplanin-positive cells. When the formed cell aggregates were dispersed, cell aggregates and organoid-like aggregates were reformed. Comparing 3D-culture and adhesion culture (2D-culture), SP-C expression of 10 d of cells was maintained. Expression of markers of undifferentiated markers and alveolar tissue stem cells decreased when cell aggregates were cultured with the addition of fetal bovine serum.

Indexed as

AnimalsBiomarkersCell AdhesionCell AggregationCell DifferentiationCells, CulturedCell ShapeGene Expression RegulationMice, Inbred C57BLPulmonary AlveoliRespiratory MucosaStaining and LabelingStem CellsBiomarkersAlveolar epithelium like cellCell aggregateLungOrganoidSelf-reconstitutionTissue stem cell

Identifiers

PMID30145679
OpenAlexW2888212440

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.