Evidence map›Paper›PMID 20585452›Full record

ArticlePloS one2010

Protective unfolded protein response in human pancreatic beta cells transplanted into mice.

Jeffrey Kennedy, Hitoshi Katsuta, Min-Ho Jung, Lorella Marselli, Allison B Goldfine, Ulysses J Balis, Dennis Sgroi, Susan Bonner-Weir, Gordon C Weir

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

18 citing papers in PubMed, 31 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Laser capture microdissection for protein and NanoString RNA analysis.Methods in molecular biology (Clifton, N.J.) · 2013
    Article
  15. Article
  16. Article
  17. Endoplasmic reticulum stress and pancreatic β-cell death.Trends in endocrinology and metabolism: TEM · 2011
    Review
  18. β-Cell failure in type 2 diabetes.Journal of diabetes investigation · 2011
    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.

Jeffrey KennedySection on Islet Cell Biology and Regenerative Medicine, Research Division, Joslin Diabetes Center, and the Department of Medicine, Harvard Medical School, Boston, Massachusetts, United States of America.
Hitoshi Katsuta
Min-Ho Jung
Lorella Marselli
Allison B Goldfine
Ulysses J Balis
Dennis Sgroi
Susan Bonner-Weir
Gordon C Weir
Joslin Diabetes Center · USHarvard University · US

Funding

SPECIAL ASSAY COREP30DK036836 · NIDDK · JOSLIN DIABETES CENTER · PI JEAN E. SCHAFFER · 1986 to 2026
$50.5M
Phenotypic Analysis of Young and Old Beta CellsR01DK066056 · NIDDK · JOSLIN DIABETES CENTER · PI BONNER-WEIR, SUSAN · 2005 to 2008
$1.1M
NIDDK NIH HHS P30 DK036836NIDDK NIH HHS P30 DK36836NIDDK NIH HHS R01 DK066056NIDDK NIH HHS R01 DK66056
6 · The paper itself

Abstract

backgroundThere is great interest about the possible contribution of ER stress to the apoptosis of pancreatic beta cells in the diabetic state and with islet transplantation. METHODS AND

findingsExpression of genes involved in ER stress were examined in beta cell enriched tissue obtained with laser capture microdissection (LCM) from frozen sections of pancreases obtained from non-diabetic subjects at surgery and from human islets transplanted into ICR-SCID mice for 4 wk. Because mice have higher glucose levels than humans, the transplanted beta cells were exposed to mild hyperglycemia and the abnormal environment of the transplant site. RNA was extracted from the LCM specimens, amplified and then subjected to microarray analysis. The transplanted beta cells showed an unfolded protein response (UPR). There was activation of many genes of the IRE-1 pathway that provide protection against the deleterious effects of ER stress, increased expression of ER chaperones and ERAD (ER-associated protein degradation) proteins. The other two arms of ER stress, PERK and ATF-6, had many down regulated genes. Downregulation of EIF2A could protect by inhibiting protein synthesis. Two genes known to contribute to apoptosis, CHOP and JNK, were downregulated.

conclusionsHuman beta cells in a transplant site had UPR changes in gene expression that protect against the proapoptotic effects of unfolded proteins.

Indexed as

Islets of Langerhans TransplantationMice, Inbred ICRProtein DenaturationAnimalsApoptosisBlood GlucoseEndoplasmic ReticulumHumansIslets of LangerhansMiceMice, SCIDBlood Glucose

Identifiers

PMID20585452
PMCPMC2887848
OpenAlexW2147252435

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.