Evidence map›Paper›PMID 21240476›Full record

ArticleDiabetologia2011

Rat neonatal beta cells lack the specialised metabolic phenotype of mature beta cells.

A Jermendy, E Toschi, T Aye, A Koh, C Aguayo-Mazzucato, A Sharma, G C Weir, D Sgroi, S Bonner-Weir

Abstract read
In one paragraph

Article in Diabetologia, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
–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

79 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Article

19 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

9 authors.

A JermendySection on Islet Cell and Regenerative Biology, Research Division, Joslin Diabetes Center, Department of Medicine, Harvard Medical School, One Joslin Place, Boston, MA 02215, USA.
E Toschi
T Aye
A Koh
C Aguayo-Mazzucato
A Sharma
G C Weir
D Sgroi
S Bonner-Weir

Funding

SPECIAL ASSAY COREP30DK036836 · NIDDK · JOSLIN DIABETES CENTER · PI JEAN E. SCHAFFER · 1986 to 2026
$50.5M
Restoration of Endocrine Pancreas FunctionU19DK061251 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI HABENER, JOEL F · 2001 to 2004
$3.0M
Physiological Factors Driving Maturation of Neonatal Beta CellsR01DK093909 · NIDDK · JOSLIN DIABETES CENTER · PI BONNER-WEIR, SUSAN · 2011 to 2015
$1.8M
Phenotypic Analysis of Young and Old Beta CellsR01DK066056 · NIDDK · JOSLIN DIABETES CENTER · PI BONNER-WEIR, SUSAN · 2005 to 2008
$1.1M
NIDDK NIH HHS DK 61251NIDDK NIH HHS P30 DK036836NIDDK NIH HHS P30 DK 36836NIDDK NIH HHS R01 DK066056NIDDK NIH HHS R01 DK093909NIDDK NIH HHS R01 DK 66056NIDDK NIH HHS U19 DK061251
6 · The paper itself

Abstract

aims/hypothesisFetal and neonatal beta cells have poor glucose-induced insulin secretion and only gain robust glucose responsiveness several weeks after birth. We hypothesise that this unresponsiveness is due to a generalised immaturity of the metabolic pathways normally found in beta cells rather than to a specific defect.

methodsUsing laser-capture microdissection we excised beta cell-enriched cores of pancreatic islets from day 1 (P1) neonatal and young adult Sprague-Dawley rats in order to compare their gene-expression profiles using Affymetrix U34A microarrays (neonatal, n = 4; adult, n = 3).

resultsUsing dChip software for analysis, 217 probe sets for genes/38 expressed sequence tags (ESTs) were significantly higher and 345 probe sets for genes/33 ESTs significantly lower in beta cell-enriched cores of neonatal islets compared with those of adult islets. Among the genes lower in the neonatal beta cells were key metabolic genes including mitochondrial shuttles (malate dehydrogenase, glycerol-3-phosphate dehydrogenase and glutamate oxalacetate transaminase), pyruvate carboxylase and carnitine palmitoyl transferase 2. Differential expression of these enzyme genes was confirmed by quantitative PCR on RNA from isolated neonatal (P2 until P28) and adult islets and with immunostaining of pancreas. Even by 28 days of age some of these genes were still expressed at lower levels than in adults. CONCLUSIONS/

interpretationThe lack of glucose responsiveness in neonatal islets is likely to be due to a generalised immaturity of the metabolic specialisation of pancreatic beta cells.

Indexed as

AnimalsAnimals, NewbornAspartate AminotransferasesExpressed Sequence TagsFemaleGlycerolphosphate DehydrogenaseInsulin-Secreting CellsIn Vitro TechniquesIslets of LangerhansMalate DehydrogenaseMaleMicrodissectionOligonucleotide Array Sequence AnalysisRatsRats, Sprague-DawleyReverse Transcriptase Polymerase Chain ReactionAspartate AminotransferasesGlycerolphosphate DehydrogenaseMalate Dehydrogenase

Identifiers

PMID21240476
PMCPMC3045081

What OpenQuestion holds

Textmetadata
LicenceTDM
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.