Evidence map›Paper›PMID 24135142›Full record

ArticleThe Journal of clinical investigation2013

Human iPS cell-derived alveolar epithelium repopulates lung extracellular matrix.

Mahboobe Ghaedi, Elizabeth A Calle, Julio J Mendez, Ashley L Gard, Jenna Balestrini, Adam Booth, Peter F Bove, Liqiong Gui, Eric S White, Laura E Niklason

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 121 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
121citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

121 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. HumanTissue barriers · 2024
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Stem cell-based therapy for pulmonary fibrosis.Stem cell research & therapy · 2022
    Review
  16. Expandable Lung Epithelium Differentiated from Human Embryonic Stem Cells.Tissue engineering and regenerative medicine · 2022
    Article
  17. Review
  18. Article
  19. Article
  20. Article

61 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

10 authors.

Mahboobe Ghaedi
Elizabeth A Calle
Julio J Mendez
Ashley L Gard
Jenna Balestrini
Adam Booth
Peter F Bove
Liqiong Gui
Eric S White
Laura E Niklason

Funding

Research Training in AnesthesiaT32GM086287 · NIGMS · YALE UNIVERSITY · PI ROBERT SCHONBERGER · 2009 to 2026
$3.7M
Matrix and Bioreactors for Human Lung RegenerationU01HL111016 · NHLBI · YALE UNIVERSITY · PI NIKLASON, LAURA E, WHITE, ERIC S · 2012 to 2016
$3.2M
Lung Tissue EngineeringR01HL098220 · NHLBI · YALE UNIVERSITY · PI NIKLASON, LAURA E · 2010 to 2013
$2.5M
NHLBI NIH HHS R01 HL098220NHLBI NIH HHS U01 HL111016NIGMS NIH HHS T32 GM086287
6 · The paper itself

Abstract

The use of induced pluripotent stem cells (iPSCs) has been postulated to be the most effective strategy for developing patient-specific respiratory epithelial cells, which may be valuable for lung-related cell therapy and lung tissue engineering. We generated a relatively homogeneous population of alveolar epithelial type II (AETII) and type I (AETI) cells from human iPSCs that had phenotypic properties similar to those of mature human AETII and AETI cells. We used these cells to explore whether lung tissue can be regenerated in vitro. Consistent with an AETII phenotype, we found that up to 97% of cells were positive for surfactant protein C, 95% for mucin-1, 93% for surfactant protein B, and 89% for the epithelial marker CD54. Additionally, exposing induced AETII to a Wnt/β-catenin inhibitor (IWR-1) changed the iPSC-AETII-like phenotype to a predominantly AETI-like phenotype. We found that of induced AET1 cells, more than 90% were positive for type I markers, T1α, and caveolin-1. Acellular lung matrices were prepared from whole rat or human adult lungs treated with decellularization reagents, followed by seeding these matrices with alveolar cells derived from human iPSCs. Under appropriate culture conditions, these progenitor cells adhered to and proliferated within the 3D lung tissue scaffold and displayed markers of differentiated pulmonary epithelium.

Indexed as

Alveolar Epithelial CellsAnimalsBiomarkersCell AdhesionCell DifferentiationCell ProliferationExtracellular MatrixHumansInduced Pluripotent Stem CellsMiceMucin-1Pulmonary AlveoliPulmonary Surfactant-Associated Protein BPulmonary Surfactant-Associated Protein CRatsTissue EngineeringBiomarkersMucin-1Pulmonary Surfactant-Associated Protein BPulmonary Surfactant-Associated Protein CSFTPC protein, human

Identifiers

PMID24135142
PMCPMC3809786

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.