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Leprdb Mouse Model of Type 2 Diabetes: Pancreatic Islet Isolation and Live-cell 2-Photon Imaging Of Intact Islets
Published on: May 11, 2015
Controlled type II diabetes mellitus has no major influence on platelet micro-RNA expression. Results from
Christian Stratz1, Thomas Nührenberg, Bernd L Fiebich
1Christian Stratz, Universitäts-Herzzentrum Freiburg - Bad Krozingen, Abteilung für Kardiologie und Angiologie II, Südring 15, D-79189 Bad Krozingen, Germany, Tel.: +49 7633 4020, Fax: +49 761 4022489,
Abstract:
Diabetes mellitus as a major contributor to cardiovascular disease burden induces dysfunctional platelets. Platelets contain abundant miRNAs, which are linked to inflammatory responses and, thus, may play a role in atherogenesis. While diabetes mellitus affects plasma miRNAs, no data exist on platelet miRNA profiles in this disease. Therefore, this study sought to explore the miRNA profile of platelets in patients with diabetes mellitus that is unrelated to the presence or absence of coronary artery disease (CAD). Platelet miRNA profiles were assessed in stable diabetic and non-diabetic patients (each n=30); 15 patients in each group had CAD. Platelet miRNA was isolated from leucocyte-depleted platelet-rich plasma, and miRNA profiling was performed using LNA micro-array technology (miRBase18.0, containing 1,917 human miRNAs). Effects of diabetes mellitus were explored by univariate statistical tests for each miRNA, adjusted for potential confounders, and by developing a multivariable signature; evaluated by resampling techniques. Platelets in non-diabetic patients demonstrated miRNA expression profiles comparable to previous data. The miRNA profiles of platelets in diabetics were similar. Statistical analysis unveiled three miRNAs (miR-377-5p, miR-628-3p, miR-3137) with high reselection probabilities in resampling techniques, corresponding to signatures with modest discriminatory performance. Functional annotation of predicted targets for these miRNAs pointed towards an influence of diabetes mellitus on mRNA processing. We did not find major differences in platelet miRNA profiles between diabetics and non-diabetics. Minor differences pertained to miRNAs associated with mRNA processing. Thus, described differences in plasma miRNAs between diabetic and non-diabetic patients cannot be explained by plain changes in platelet miRNA profile.
Insights
Diabetes mellitus does not significantly alter platelet microRNA (miRNA) profiles, contrary to plasma changes. Minor differences in platelet miRNA related to mRNA processing were observed in diabetic patients.
Area of Science:
- Cardiovascular Biology
- Molecular Biology
- Endocrinology
Background:
- Diabetes mellitus is a major risk factor for cardiovascular disease.
- Platelets contain microRNAs (miRNAs) involved in inflammation and atherogenesis.
- Plasma miRNA profiles differ in diabetes, but platelet miRNA profiles remain uncharacterized.
Purpose of the Study:
- To investigate platelet miRNA profiles in patients with diabetes mellitus.
- To determine if diabetes mellitus, independent of coronary artery disease (CAD), affects platelet miRNA expression.
Main Methods:
- Platelet miRNA profiling was performed using LNA micro-array technology on stable diabetic and non-diabetic patients.
- Statistical analyses, including univariate tests and multivariable signature development with resampling, were used.
- miRNA expression was compared between groups, with and without CAD.
Main Results:
- Platelet miRNA profiles were largely similar between diabetic and non-diabetic individuals.
- Three specific miRNAs (miR-377-5p, miR-628-3p, miR-3137) showed minor differences linked to mRNA processing.
- No major differences in platelet miRNA profiles explained observed plasma miRNA alterations in diabetes.
Conclusions:
- Diabetes mellitus does not cause substantial changes in platelet miRNA profiles.
- Observed differences in plasma miRNAs in diabetes are not attributable to altered platelet miRNA expression.
- Further research is needed to understand the role of platelet miRNAs in diabetic cardiovascular complications.
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