Evidence map›Paper›PMID 35245441›Full record

ArticleStem cell reports2022

Development of a scalable method to isolate subsets of stem cell-derived pancreatic islet cells.

Audrey V Parent, Sudipta Ashe, Gopika G Nair, Mei-Lan Li, Jessica Chavez, Jennifer S Liu, Yongping Zhong, Philip R Streeter, Matthias Hebrok

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

20 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
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  6. Article
  7. Review
  8. The Last Mile in Beta-Cell Replacement Therapy for Type 1 Diabetes: Time to Grow Up.Transplant international : official journal of the European Society for Organ Transplantation · 2025
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Stem Cell-Derived Islets for Type 2 Diabetes.International journal of molecular sciences · 2022
    Review
  20. Strategies to Improve the Safety of iPSC-Derived β Cells for β Cell Replacement in Diabetes.Transplant international : official journal of the European Society for Organ Transplantation · 2022
    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

9 authors at 2 institutions in 1 country.

Audrey V ParentDiabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA. Electronic address: audrey.parent@ucsf.edu.
Sudipta AsheDiabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA.
Gopika G NairDiabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA.
Mei-Lan LiDiabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA.
Jessica ChavezDiabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA.
Jennifer S LiuDiabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA.
Yongping ZhongOregon Stem Cell Center, Oregon Health and Science University, Portland, OR 97239, USA.
Philip R StreeterOregon Stem Cell Center, Oregon Health and Science University, Portland, OR 97239, USA.
Matthias HebrokDiabetes Center, Department of Medicine, University of California, San Francisco, San Francisco, CA 94143, USA. Electronic address: matthias.hebrok@ucsf.edu.
University of California, San Francisco · USOregon Health & Science University · US

Funding

Research BaseP30DK063720 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VAISSE, CHRISTIAN · 2003 to 2019
$21.8M
Molecular Pathology of CancerT32CA177555 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BASTIAN, BORIS C., OAKES, SCOTT A. · 2013 to 2017
$1.1M
NCI NIH HHS T32 CA177555NIDDK NIH HHS P30 DK063720
6 · The paper itself

Abstract

Cell replacement therapy using β cells derived from stem cells is a promising alternative to conventional diabetes treatment options. Although current differentiation methods produce glucose-responsive β cells, they can also yield populations of undesired endocrine progenitors and other proliferating cell types that might interfere with long-term islet function and safety of transplanted cells. Here, we describe the generation of an array of monoclonal antibodies against cell surface markers that selectively label stem cell-derived islet cells. A high-throughput screen identified promising candidates, including three clones that mark a high proportion of endocrine cells in differentiated cultures. A scalable magnetic sorting method was developed to enrich for human pluripotent stem cell (hPSC)-derived islet cells using these three antibodies, leading to the formation of islet-like clusters with improved glucose-stimulated insulin secretion and reduced growth upon transplantation. This strategy should facilitate large-scale production of functional islet clusters from stem cells for disease modeling and cell replacement therapy.

Indexed as

Insulin-Secreting CellsIslets of LangerhansPluripotent Stem CellsCell DifferentiationGlucoseHumansInsulinInsulin SecretionGlucoseInsulincell therapydiabetesdirected differentiationpancreatic beta cellsregenerative medicine

Identifiers

PMID35245441
PMCPMC9023773
OpenAlexW4214860699

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.