Evidence map›Paper›PMID 28784128›Full record

ArticleRespiratory research2017

Fraction of MHCII and EpCAM expression characterizes distal lung epithelial cells for alveolar type 2 cell isolation.

Koichi Hasegawa, Atsuyasu Sato, Kazuya Tanimura, Kiyoshi Uemasu, Yoko Hamakawa, Yoshinori Fuseya, Susumu Sato, Shigeo Muro, Toyohiro Hirai

Open access · goldAbstract read
In one paragraph

Article in Respiratory research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

64 citing papers in PubMed, 112 citations in OpenAlex.

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4 more citing papers are in PubMed but not listed here.

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 1 country.

Koichi HasegawaDepartment of Respiratory Medicine, Kyoto University Graduate School of Medicine, 54 Kawahara Shogoin Sakyo, Kyoto, 606-8507, Japan.
Atsuyasu SatoDepartment of Respiratory Medicine, Kyoto University Graduate School of Medicine, 54 Kawahara Shogoin Sakyo, Kyoto, 606-8507, Japan. atsuyasu@kuhp.kyoto-u.ac.jp.ORCID 0000-0001-8068-9984
Kazuya TanimuraPulmonary Medicine, Kishiwada City Hospital, 1001 Gakuhara Kishiwada, Osaka, 596-8501, Japan.
Kiyoshi UemasuDepartment of Respiratory Medicine, Kyoto University Graduate School of Medicine, 54 Kawahara Shogoin Sakyo, Kyoto, 606-8507, Japan.
Yoko HamakawaDepartment of Respiratory Medicine, Kyoto University Graduate School of Medicine, 54 Kawahara Shogoin Sakyo, Kyoto, 606-8507, Japan.
Yoshinori FuseyaPulmonary Medicine, Otsu City Hospital, 2 Chome-9-9 Motomiya Otsu, Shiga, 520-0804, Japan.
Susumu SatoDepartment of Respiratory Medicine, Kyoto University Graduate School of Medicine, 54 Kawahara Shogoin Sakyo, Kyoto, 606-8507, Japan.
Shigeo MuroDepartment of Respiratory Medicine, Kyoto University Graduate School of Medicine, 54 Kawahara Shogoin Sakyo, Kyoto, 606-8507, Japan.
Toyohiro HiraiDepartment of Respiratory Medicine, Kyoto University Graduate School of Medicine, 54 Kawahara Shogoin Sakyo, Kyoto, 606-8507, Japan.
Kyoto University · JPKishiwada City Hospital · JPOtsu Municipal Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgoundAlveolar type 2 (AT2) cells play important roles in maintaining adult lung homeostasis. AT2 cells isolated from the lung have revealed the cell-specific functions of AT2 cells. Comprehensive molecular and transcriptional profiling of purified AT2 cells would be helpful for elucidating the underlying mechanisms of their cell-specific functions. To enable the further purification of AT2 cells, we aimed to discriminate AT2 cells from non-AT2 lung epithelial cells based on surface antigen expression via fluorescence activated cell sorting (FACS).

methodsSingle-cell suspensions obtained from enzymatically digested murine lungs were labeled for surface antigens (CD45/CD31/epithelial cell adhesion molecule (EpCAM)/ major histocompatibility complex class II (MHCII)) and for pro-surfactant protein C (proSP-C), followed by FACS analysis for surface antigen expression on AT2 cells. AT2 cells were sorted, and purity was evaluated by immunofluorescence and FACS. This newly developed strategy for AT2 cell isolation was validated in different strains and ages of mice, as well as in a lung injury model.

resultsFACS analysis revealed that EpCAM

conclusionsWe successfully classified murine distal lung epithelial cells based on EpCAM and MHCII expression. The discrimination of AT2 cells from non-AT2 epithelial cells resulted in the isolation of pure AT2 cells. Highly pure AT2 cells will provide accurate and deeper insights into the cell-specific mechanisms of alveolar homeostasis.

Indexed as

Alveolar Epithelial CellsAnimalsCell CountCell DifferentiationCells, CulturedCell SeparationEpithelial Cell Adhesion MoleculeFlow CytometryGene ExpressionGenes, MHC Class IIMiceMice, Inbred BALB CMice, Inbred C57BLMice, TransgenicEpithelial Cell Adhesion MoleculeAlveolar type 2 cellCell isolationEpCAMMCHII

Identifiers

PMID28784128
PMCPMC5545863
OpenAlexW2744103874

What OpenQuestion holds

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LicenceCC BY
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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.