Oxidative stress decreases microtubule growth and stability in ventricular myocytes. (April 2016)

• Record Type: Journal Article
• Authors: Drum, Benjamin M.L.; Yuan, Can; Li, Lei; Liu, Qinghang; Wordeman, Linda; Santana, L. Fernando
• Is Part Of: Journal of molecular and cellular cardiology. Volume 93(2016:Apr.)
• Page Start: 32
• Page End: 43
• Publication Date: 2016-04
• Subjects: Microtubule dynamics -- Cardiomyocytes -- Live imaging -- Oxidative stress -- Myocardial infarction -- Transient outward current; Cardiology -- Periodicals; Heart Diseases -- Periodicals; Molecular Biology -- Periodicals; Cardiologie -- Périodiques; Cardiology; Electronic journals; Periodicals; 616.12
• DOI: 10.1016/j.yjmcc.2016.02.012
• Languages: English
• ISSNs: 0022-2828

Abstract

Abstract: Microtubules (MTs) have many roles in ventricular myocytes, including structural stability, morphological integrity, and protein trafficking. However, despite their functional importance, dynamic MTs had never been visualized in living adult myocytes. Using adeno-associated viral vectors expressing the MT-associated protein plus end binding protein 3 (EB3) tagged with EGFP, we were able to perform live imaging and thus capture and quantify MT dynamics in ventricular myocytes in real time under physiological conditions. Super-resolution nanoscopy revealed that EB1 associated in puncta along the length of MTs in ventricular myocytes. The vast (~ 80%) majority of MTs grew perpendicular to T-tubules at a rate of 0.06 μm ∗ s − 1 and growth was preferentially (82%) confined to a single sarcomere. Microtubule catastrophe rate was lower near the Z-line than M-line. Hydrogen peroxide increased the rate of catastrophe of MTs ~ 7-fold, suggesting that oxidative stress destabilizes these structures in ventricular myocytes. We also quantified MT dynamics after myocardial infarction (MI), a pathological condition associated with increased production of reactive oxygen species (ROS). Our data indicate that the catastrophe rate of MTs increases following MI. This contributed to decreased transient outward K + currents by decreasing the surface expression of Kv 4.2 and Kv 4.3 channels after MI. On the basis of these data, we conclude that, under physiological conditions, MT growth is directionally biased and that increased ROS production during MI disrupts MT dynamics, decreasing K + channel trafficking. Highlights: EB1 and EB3 associate in puncta along the length of MTs. MTs grow mainly perpendicular to T-tubules. MT dynamics are temperature dependent. Oxidative stress disrupts MT dynamics in cardiomyocytes during MI. MT destabilization reduces I to by decreasing KV 4.2 and KV 4.3 surface expression.