Phenotypic Characterization of MIP-CreERT1Lphi Mice With Transgene-Driven Islet Expression of Human Growth Hormone.

Journal Article (Journal Article)

There is growing concern over confounding artifacts associated with β-cell-specific Cre-recombinase transgenic models, raising questions about their general usefulness in research. The inducible β-cell-specific transgenic (MIP-CreERT(1Lphi)) mouse was designed to circumvent many of these issues, and we investigated whether this tool effectively addressed concerns of ectopic expression and disruption of glucose metabolism. Recombinase activity was absent from the central nervous system using a reporter line and high-resolution microscopy. Despite increased pancreatic insulin content, MIP-CreERT mice on a chow diet exhibited normal ambient glycemia, glucose tolerance and insulin sensitivity, and appropriate insulin secretion in response to glucose in vivo and in vitro. However, MIP-CreERT mice on different genetic backgrounds were protected from high-fat/ streptozotocin (STZ)-induced hyperglycemia that was accompanied by increased insulin content and islet density. Ectopic human growth hormone (hGH) was highly expressed in MIP-CreERT islets independent of tamoxifen administration. Circulating insulin levels remained similar to wild-type controls, whereas STZ-associated increases in α-cell number and serum glucagon were significantly blunted in MIP-CreERT(1Lphi) mice, possibly due to paracrine effects of hGH-induced serotonin expression. These studies reveal important new insight into the strengths and limitations of the MIP-CreERT mouse line for β-cell research.

Full Text

Duke Authors

Cited Authors

  • Oropeza, D; Jouvet, N; Budry, L; Campbell, JE; Bouyakdan, K; Lacombe, J; Perron, G; Bergeron, V; Neuman, JC; Brar, HK; Fenske, RJ; Meunier, C; Sczelecki, S; Kimple, ME; Drucker, DJ; Screaton, RA; Poitout, V; Ferron, M; Alquier, T; Estall, JL

Published Date

  • November 2015

Published In

Volume / Issue

  • 64 / 11

Start / End Page

  • 3798 - 3807

PubMed ID

  • 26153246

Pubmed Central ID

  • PMC4613972

Electronic International Standard Serial Number (EISSN)

  • 1939-327X

Digital Object Identifier (DOI)

  • 10.2337/db15-0272


  • eng

Conference Location

  • United States