Alterations in lung gene expression in streptozotocin-induced diabetic rats

Erik van Lunteren1, Michelle Moyer, Sarah Spiegler

  • 1Pulmonary, Critical Care and Sleep Division, Department of Medicine, Louis Stokes Cleveland Department of Veterans Affairs Medical Center, Case Western Reserve University, 10701 East Boulevard, Cleveland, OH 44106, USA. exv4@cwru.edu.

BMC Endocrine Disorders
|January 16, 2014
PubMed
Abstract

Insights

Type 1 diabetes alters lung gene expression, impacting apoptosis and stress responses. However, the lung shows resistance to metabolic and oxidative stress gene changes seen in other organs.

Area of Science:

  • Molecular Biology
  • Genomics
  • Physiology

Background:

  • Diabetes mellitus significantly impacts gene expression across multiple organs, affecting metabolism, oxidative stress, and protein ubiquitination.
  • Type 1 diabetes is known to impair lung function, but its effects on lung gene expression remain largely uncharacterized.

Purpose of the Study:

  • To investigate the impact of type 1 diabetes on gene expression in the lung.
  • To compare lung gene expression changes in diabetes with those observed in other affected organs.

Main Methods:

  • Gene expression microarray analysis was performed on lung tissue from a rat model of streptozotocin-induced diabetes mellitus.

Main Results:

  • Diabetic rats exhibited significantly elevated glucose levels compared to controls.
  • Microarray analysis revealed 46 genes with significantly altered expression (19 increased, 27 decreased).
  • Over-represented gene ontology groups included apoptosis, response to stress, protein kinase activity, ion transporter activity, and collagen, with distinct patterns of expression changes.

Conclusions:

  • Type 1 diabetes affects specific areas of lung gene expression, notably apoptosis and stress responses.
  • The lung demonstrates resistance to the metabolic and oxidative stress-related gene expression alterations observed in other diabetic tissues like the heart, skeletal muscle, and kidney.