Evidence map›Paper›PMID 28239758›Full record

ArticleStem cell reviews and reports2017

Acellular Mouse Kidney ECM can be Used as a Three-Dimensional Substrate to Test the Differentiation Potential of Embryonic Stem Cell Derived Renal Progenitors.

Manpreet Sambi, Theresa Chow, Jennifer Whiteley, Mira Li, Shawn Chua, Vanessa Raileanu, Ian M Rogers

Open access · hybridAbstract read
In one paragraph

Article in Stem cell reviews and reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
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  5. Article
  6. Review
  7. Article
  8. Review
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  13. Article
  14. Growing a new human kidney.Kidney international · 2019
    Review
  15. Advances in the Knowledge about Kidney Decellularization and Repopulation.Frontiers in bioengineering and biotechnology · 2017
    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

7 authors at 3 institutions in 1 country.

Manpreet SambiWomen's and Infant's Health, Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital and University of Toronto, 60 Murray St, Box 40, Toronto, ON, M5T 3L9, Canada.
Theresa ChowWomen's and Infant's Health, Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital and University of Toronto, 60 Murray St, Box 40, Toronto, ON, M5T 3L9, Canada.
Jennifer WhiteleyWomen's and Infant's Health, Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital and University of Toronto, 60 Murray St, Box 40, Toronto, ON, M5T 3L9, Canada.
Mira LiWomen's and Infant's Health, Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital and University of Toronto, 60 Murray St, Box 40, Toronto, ON, M5T 3L9, Canada.
Shawn ChuaWomen's and Infant's Health, Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital and University of Toronto, 60 Murray St, Box 40, Toronto, ON, M5T 3L9, Canada.
Vanessa RaileanuWomen's and Infant's Health, Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital and University of Toronto, 60 Murray St, Box 40, Toronto, ON, M5T 3L9, Canada.
Ian M RogersWomen's and Infant's Health, Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital and University of Toronto, 60 Murray St, Box 40, Toronto, ON, M5T 3L9, Canada. Irogers@lunenfeld.ca.
University of Toronto · CALunenfeld-Tanenbaum Research Institute · CAMount Sinai Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of strategies for tissue regeneration and bio-artificial organ development is based on our understanding of embryogenesis. Differentiation protocols attempt to recapitulate the signaling modalities of gastrulation and organogenesis, coupled with cell selection regimens to isolate the cells of choice. This strategy is impeded by the lack of optimal in vitro culture systems since traditional culture systems do not allow for the three-dimensional interaction between cells and the extracellular matrix. While artificial three-dimensional scaffolds are available, using the natural extracellular matrix scaffold is advantageous because it has a distinct architecture that is difficult to replicate. The adult extracellular matrix is predicted to mediate signaling related to tissue repair not embryogenesis but existing similarities between the two argues that the extracellular matrix will influence the differentiation of stem and progenitor cells. Previous studies using undifferentiated embryonic stem cells grown directly on acellular kidney ECM demonstrated that the acellular kidney supported cell growth but limited differentiation occurred. Using mouse kidney extracellular matrix and mouse embryonic stem cells we report that the extracellular matrix can support the development of kidney structures if the stem cells are first differentiated to kidney progenitor cells before being applied to the acellular organ.

Indexed as

Cell DifferentiationMouse Embryonic Stem CellsAnimalsExtracellular MatrixKidneyMiceAcellularDecellularized kidneyExtracellular matrixKidneyOrgan culturePluripotent cellsSix2 +Stem cells

Identifiers

PMID28239758
PMCPMC5493730
OpenAlexW2590914909

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.