Evidence map›Paper›PMID 24763685›Full record

ArticleStem cells translational medicine2014

Differentiation of mouse induced pluripotent stem cells into alveolar epithelial cells in vitro for use in vivo.

Qiliang Zhou, Xulu Ye, Ruowen Sun, Yoshifumi Matsumoto, Masato Moriyama, Yoshiya Asano, Yoichi Ajioka, Yasuo Saijo

Open access · goldAbstract read
In one paragraph

Article in Stem cells translational medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

26 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Induced pluripotent stem cell-based therapies for organ fibrosis.Frontiers in bioengineering and biotechnology · 2023
    Review
  6. Stem cell-based therapy for pulmonary fibrosis.Stem cell research & therapy · 2022
    Review
  7. Expandable Lung Epithelium Differentiated from Human Embryonic Stem Cells.Tissue engineering and regenerative medicine · 2022
    Article
  8. Review
  9. Review
  10. Review
  11. Targeting Alveolar Repair in Idiopathic Pulmonary Fibrosis.American journal of respiratory cell and molecular biology · 2021
    Review
  12. [Research and Application of Stem Cell-Based Therapy in Idiopathic Pulmonary Fibrosis: A Review].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2021
    Review
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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

8 authors at 3 institutions in 2 countries.

Qiliang ZhouDepartment of Medical Oncology and Division of Molecular and Diagnostic Pathology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan; Department of Pediatric Hematology, Shengjing Hospital of China Medical University, Shenyang, People's Republic of China; Department of Neuroanatomy, Cell Biology, and Histology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Xulu YeDepartment of Medical Oncology and Division of Molecular and Diagnostic Pathology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan; Department of Pediatric Hematology, Shengjing Hospital of China Medical University, Shenyang, People's Republic of China; Department of Neuroanatomy, Cell Biology, and Histology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Ruowen SunDepartment of Medical Oncology and Division of Molecular and Diagnostic Pathology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan; Department of Pediatric Hematology, Shengjing Hospital of China Medical University, Shenyang, People's Republic of China; Department of Neuroanatomy, Cell Biology, and Histology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Yoshifumi MatsumotoDepartment of Medical Oncology and Division of Molecular and Diagnostic Pathology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan; Department of Pediatric Hematology, Shengjing Hospital of China Medical University, Shenyang, People's Republic of China; Department of Neuroanatomy, Cell Biology, and Histology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Masato MoriyamaDepartment of Medical Oncology and Division of Molecular and Diagnostic Pathology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan; Department of Pediatric Hematology, Shengjing Hospital of China Medical University, Shenyang, People's Republic of China; Department of Neuroanatomy, Cell Biology, and Histology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Yoshiya AsanoDepartment of Medical Oncology and Division of Molecular and Diagnostic Pathology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan; Department of Pediatric Hematology, Shengjing Hospital of China Medical University, Shenyang, People's Republic of China; Department of Neuroanatomy, Cell Biology, and Histology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Yoichi AjiokaDepartment of Medical Oncology and Division of Molecular and Diagnostic Pathology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan; Department of Pediatric Hematology, Shengjing Hospital of China Medical University, Shenyang, People's Republic of China; Department of Neuroanatomy, Cell Biology, and Histology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Yasuo SaijoDepartment of Medical Oncology and Division of Molecular and Diagnostic Pathology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan; Department of Pediatric Hematology, Shengjing Hospital of China Medical University, Shenyang, People's Republic of China; Department of Neuroanatomy, Cell Biology, and Histology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan yasosj@med.niigata-u.ac.jp.
Niigata University · JPChina Medical University · CNHirosaki University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alveolar epithelial cells (AECs) differentiated from induced pluripotent stem cells (iPSCs) represent new opportunities in lung tissue engineering and cell therapy. In this study, we modified a two-step protocol for embryonic stem cells that resulted in a yield of ∼9% surfactant protein C (SPC)(+) alveolar epithelial type II (AEC II) cells from mouse iPSCs in a 12-day period. The differentiated iPSCs showed morphological characteristics similar to those of AEC II cells. When differentiated iPSCs were seeded and cultured in a decellularized mouse lung scaffold, the cells reformed an alveolar structure and expressed SPC or T1α protein (markers of AEC II or AEC I cells, respectively). Finally, the differentiated iPSCs were instilled intratracheally into a bleomycin-induced mouse acute lung injury model. The transplanted cells integrated into the lung alveolar structure and expressed SPC and T1α. Significantly reduced lung inflammation and decreased collagen deposition were observed following differentiated iPSC transplantation. In conclusion, we report a simple and rapid protocol for in vitro differentiation of mouse iPSCs into AECs. Differentiated iPSCs show potential for regenerating three-dimensional alveolar lung structure and can be used to abrogate lung injury.

Indexed as

Cell DifferentiationRegenerationAlveolar Epithelial CellsAnimalsBiomarkersBleomycinCell LineDisease Models, AnimalFemaleGene Expression Regulation, DevelopmentalInduced Pluripotent Stem CellsIntercellular Signaling Peptides and ProteinsMiceMice, Inbred C57BLPeptidesPhenotypeBiomarkersBleomycinIntercellular Signaling Peptides and ProteinsPeptidesPulmonary Surfactant-Associated Protein CRNA, MessengerSftpc protein, mouseDifferentiationInduced pluripotent stem cellsLungStem cell transplantation

Identifiers

PMID24763685
PMCPMC4039451
OpenAlexW2006541601

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.