Evidence map›Paper›PMID 25629318›Full record

ArticlePloS one2015

Human iPS cell-derived insulin producing cells form vascularized organoids under the kidney capsules of diabetic mice.

Sudhanshu P Raikwar, Eun-Mi Kim, William I Sivitz, Chantal Allamargot, Daniel R Thedens, Nicholas Zavazava

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
9.7field-weighted citation impact, top 1% 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

28 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Molecular Therapeutics for Diabetic Kidney Disease: An Update.International journal of molecular sciences · 2024
    Review
  3. Article
  4. Review
  5. In Vivo CaBiomedicines · 2023
    Article
  6. Review
  7. Review
  8. Genome engineering and disease modelingWorld journal of stem cells · 2021
    Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Journal of biosciences · 2018
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
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

6 authors at 3 institutions in 1 country.

Sudhanshu P RaikwarDepartment of Internal Medicine, Division of Immunology, University of Iowa, Iowa City, IA, United States of America; Veterans Affairs Medical Center, Iowa City, IA, United States of America.
Eun-Mi KimDepartment of Internal Medicine, Division of Immunology, University of Iowa, Iowa City, IA, United States of America; Veterans Affairs Medical Center, Iowa City, IA, United States of America.
William I SivitzDivision of Endocrinology & Metabolism, University of Iowa, Iowa City, IA, United States of America.
Chantal AllamargotCentral Microscopy Research facility, University of Iowa, Iowa City, IA, United States of America.
Daniel R ThedensDepartment of Radiology, University of Iowa, Iowa City, IA, United States of America.
Nicholas ZavazavaDepartment of Internal Medicine, Division of Immunology, University of Iowa, Iowa City, IA, United States of America; Veterans Affairs Medical Center, Iowa City, IA, United States of America.
University of Iowa · USIowa City VA Medical Center · USVeterans Health Administration · US

Funding

Vector Core-Core 2P30DK054759 · NIDDK · UNIVERSITY OF IOWA · PI Alejandro Antonio Pezzulo · 1998 to 2026
$30.5M
EMBRYONIC STEM CELLS INDUCE SPECIFIC GRAFT TOLERANCER01HL073015 · NHLBI · UNIVERSITY OF IOWA · PI ZAVAZAVA, NICHOLAS · 2004 to 2012
$2.5M
Mitochondrial-targeted CoQ: Metabolic and Redox Effects and role in DiabetesI01BX000285 · VA · IOWA CITY VA MEDICAL CENTER · PI SIVITZ, WILLIAM IRVING · 2011 to 2017
–
BLRD VA I01 BX000285BLRD VA I01 BX001125NHLBI NIH HHS R01 HL073015NIDDK NIH HHS P30 DK054759PHS HHS R01 HLO73015
6 · The paper itself

Abstract

Type 1 diabetes (T1D) is caused by autoimmune disease that leads to the destruction of pancreatic β-cells. Transplantation of cadaveric pancreatic organs or pancreatic islets can restore normal physiology. However, there is a chronic shortage of cadaveric organs, limiting the treatment of the majority of patients on the pancreas transplantation waiting list. Here, we hypothesized that human iPS cells can be directly differentiated into insulin producing cells (IPCs) capable of secreting insulin. Using a series of pancreatic growth factors, we successfully generated iPS cells derived IPCs. Furthermore, to investigate the capability of these cells to secrete insulin in vivo, the differentiated cells were transplanted under the kidney capsules of diabetic immunodeficient mice. Serum glucose levels gradually declined to either normal or near normal levels over 150 days, suggesting that the IPCs were secreting insulin. In addition, using MRI, a 3D organoid appeared as a white patch on the transplanted kidneys but not on the control kidneys. These organoids showed neo-vascularization and stained positive for insulin and glucagon. All together, these data show that a pancreatic organ can be created in vivo providing evidence that iPS cells might be a novel option for the treatment of T1D.

Indexed as

Cell DifferentiationNeovascularization, PhysiologicStem Cell TransplantationAnimalsBlood GlucoseDiabetes Mellitus, ExperimentalHumansInduced Pluripotent Stem CellsInsulin-Secreting CellsMagnetic Resonance ImagingMaleMiceMice, KnockoutMitochondriaOrganoidsOxygen ConsumptionBlood Glucose

Identifiers

PMID25629318
PMCPMC4309616
OpenAlexW2024455909

What OpenQuestion holds

Textmetadata
LicenceCC0
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.