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Scientific article
Open access
English

INS-1 cells undergoing caspase-dependent apoptosis enhance the regenerative capacity of neighboring cells

Published inDiabetes, vol. 59, no. 11, p. 2799-2808
Publication date2010
Abstract

In diabetes, β-cell mass is not static but in a constant process of cell death and renewal. Inactivating mutations in transcription factor 1 (tcf-1)/hepatocyte nuclear factor1a (hnf1a) result in decreased β-cell mass and HNF1A-maturity onset diabetes of the young (HNF1A-MODY). Here, we investigated the effect of a dominant-negative HNF1A mutant (DN-HNF1A) induced apoptosis on the regenerative capacity of INS-1 cells.

Keywords
  • Animals
  • Apoptosis
  • Caspase 3/metabolism
  • Caspases/genetics/pharmacology
  • Cell Death/drug effects
  • Diabetes Mellitus, Type 2/genetics/physiopathology
  • Enzyme-Linked Immunosorbent Assay
  • Hepatocyte Nuclear Factor 1-alpha/genetics/pharmacology
  • Humans
  • Insulin-Secreting Cells/cytology/drug effects/physiology
  • Insulinoma/genetics
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Promoter Regions, Genetic
  • Rats
  • Reverse Transcriptase Polymerase Chain Reaction
Citation (ISO format)
BONNER, Caroline et al. INS-1 cells undergoing caspase-dependent apoptosis enhance the regenerative capacity of neighboring cells. In: Diabetes, 2010, vol. 59, n° 11, p. 2799–2808. doi: 10.2337/db09-1478
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Article (Published version)
accessLevelPublic
Identifiers
ISSN of the journal0012-1797
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313downloads

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