Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2007 Oct;50(10):2117-25.
doi: 10.1007/s00125-007-0749-2. Epub 2007 Jul 20.

Influence of diabetes on the loss of beta cell differentiation after islet transplantation in rats

Affiliations

Influence of diabetes on the loss of beta cell differentiation after islet transplantation in rats

D R Laybutt et al. Diabetologia. 2007 Oct.

Abstract

Aims/hypothesis: Hyperglycaemia can impair beta cell function after islet transplantation. Appropriate glucose-induced insulin secretion is dependent on a unique expression pattern of genes. Here we examined the effects of diabetes on gene expression in transplanted islets.

Materials and methods: Streptozotocin-induced diabetic or control non-diabetic Lewis rats were transplanted under the kidney capsule with an insufficient number (2,000) of syngeneic islets to normalise blood glucose levels in diabetic rats. Eighteen days after transplantation, islet grafts were retrieved and RT-PCR used to assess expression of selected genes critical for beta cell function. Islet grafts from diabetic rats transplanted with a sufficient number of islets (3,000) to normalise hyperglycaemia were used to assess the effects of correcting blood glucose levels. Additionally, gene expression of transplanted islets from non-diabetic rats was compared with freshly isolated islets.

Results: In islet grafts from diabetic rats, mRNA levels of several transcription factors important for the maintenance of beta cell differentiation were reduced (pancreatic and duodenal homeobox 1 [Pdx1], neurogenic differentiation 1 [Neurod1], NK6 transcription factor related, locus 1 [Nkx6.1], paired box gene 6 [Pax6]), as were genes implicated in beta cell function (Glut2 [also known as solute carrier family 2 [facilitated glucose transporter], member 2 [Slc2a2], glucokinase, insulin, islet amyloid polypeptide [Iapp]). Conversely, mRNA levels of lactate dehydrogenase, which is normally suppressed in beta cells, were increased. The majority of the changes in gene expression were normalised after correction of hyperglycaemia, indicating that the severe loss of beta cell differentiation correlates with continuous exposure to diabetes. Even islet grafts from non-diabetic rats showed a few alterations in beta cell gene expression in comparison with fresh islets.

Conclusions/interpretation: Chronic hyperglycaemia contributes to the deterioration of beta cell differentiation after islet transplantation.

PubMed Disclaimer

References

    1. Diabetologia. 1989 Sep;32(9):663-7 - PubMed
    1. J Biol Chem. 1999 May 14;274(20):14112-21 - PubMed
    1. J Biol Chem. 2003 Jan 31;278(5):2997-3005 - PubMed
    1. Diabetes. 1990 May;39(5):549-56 - PubMed
    1. J Biomed Sci. 2000 Jan-Feb;7(1):27-34 - PubMed

Publication types

MeSH terms

LinkOut - more resources