Journal article
Type 1 diabetes alters ischemia-induced gene expression
Journal of clinical & translational endocrinology, Vol.15, pp.19-24
11/22/2018
DOI: 10.1016/j.jcte.2018.11.003
PMCID: PMC6279996
PMID: 30555789
Abstract
Peripheral Artery Disease (PAD) is a chronic, activity-limiting disease that is caused by atherosclerotic occlusion of blood vessels outside the heart. Type 1 Diabetes (T1D) not only increases an individual’s likelihood of developing PAD, but also contributes to poor clinical outcomes after PAD manifestation. Although there is some evidence suggesting that hyperglycemia might alter expression of genes involved in regulating PAD severity or outcomes, our knowledge about the specific genes and pathways involved remains incomplete.
We induced experimental PAD or hind limb ischemia in T1D and non-diabetic mice and subjected the ischemic gastrocnemius muscle tissues to genome-wide mRNA transcriptome and pathway analysis. We identified 513 probe sets that represented 443 different genes with highly significant expression differences (p < 0.005) between the ischemic diabetic and ischemic non-diabetic muscle tissues. Moreover, pathway analysis of the differentially expressed genes identified pathways involved in essential biological processes such as “cell cycle,” “DNA replication,” “metabolic pathways,” “focal adhesion,” “regulation of actin cytoskeleton,” and “nucleotide excision repair”. Taken together, our data offer the opportunity to test hypotheses on the roles played by the altered genes/molecular pathways in poor PAD outcomes in diabetes. Such studies may lead to the development of specific therapies to improve PAD outcomes in patients with comorbid diabetes.
Details
- Title: Subtitle
- Type 1 diabetes alters ischemia-induced gene expression
- Creators
- Rahul Peravali - University of Tennessee Health Science CenterLucas Gunnels - University of Tennessee Health Science CenterSatyanarayana Alleboina - University of Tennessee Health Science CenterIvan C. Gerling - University of Tennessee Health Science CenterAyotunde O. Dokun - University of Tennessee Health Science Center
- Resource Type
- Journal article
- Publication Details
- Journal of clinical & translational endocrinology, Vol.15, pp.19-24
- DOI
- 10.1016/j.jcte.2018.11.003
- PMID
- 30555789
- PMCID
- PMC6279996
- NLM abbreviation
- J Clin Transl Endocrinol
- ISSN
- 2214-6237
- eISSN
- 2214-6237
- Publisher
- Elsevier
- Grant note
- DOI: 10.13039/100000050, name: National Heart, Lung, and Blood Institute, award: R01 HL130399
- Language
- English
- Date published
- 11/22/2018
- Academic Unit
- Molecular Physiology and Biophysics; Fraternal Order of Eagles Diabetes Research Center; Endocrinology and Metabolism; Internal Medicine
- Record Identifier
- 9984297498502771
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