Sympathetic denervation of pen-infarct myocardium requires the p75 neurotrophin receptor

被引:30
|
作者
Lorentz, Christina U. [1 ]
Parrish, Diana C. [1 ]
Alston, Eric N. [1 ]
Pellegrino, Michael J. [1 ]
Woodward, William R. [2 ]
Hempstead, Barbara L. [3 ]
Habecker, Beth A. [1 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Physiol & Pharmacol, Portland, OR 97239 USA
[2] Oregon Hlth & Sci Univ, Dept Neurol, Portland, OR 97239 USA
[3] Weill Cornell Med Coll, Dept Med, Div Hematol & Med Oncol, New York, NY 10065 USA
关键词
Ischemia-reperfusion; Axon degeneration; Brain-derived neurotrophic factor; Regeneration; Pruning; NERVE GROWTH-FACTOR; DOPAMINE-BETA-HYDROXYLASE; ADRENAL CHROMAFFIN CELLS; TYROSINE-HYDROXYLASE; VENTRICULAR-ARRHYTHMIAS; SELECTIVE INDUCTION; NEURITE OUTGROWTH; MICE LACKING; RAT-HEART; INNERVATION;
D O I
10.1016/j.expneurol.2013.08.015
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Development of cardiac sympathetic heterogeneity after myocardial infarction contributes to ventricular arrhythmias and sudden cardiac death. Regions of sympathetic hyperinnervation and denervation appear in the viable myocardium beyond the infarcted area. While elevated nerve growth factor (NGF) is implicated in sympathetic hyperinnervation, the mechanisms underlying denervation are unknown. Recent studies show that selective activation of the p75 neurotrophin receptor (p75(NTR)) in sympathetic neurons causes axon degeneration. We used mice that lack p75(NTR) to test the hypothesis that activation of p75(NTR) causes pen-infarct sympathetic denervation after cardiac ischemia-reperfusion. Wild type hearts exhibited sympathetic denervation adjacent to the infarct 24 h and 3 days after ischemia-reperfusion, but no pen-infarct sympathetic denervation occurred in p75(NTR)-/- mice. Sympathetic hyperinnervation was found in the distal pen-infarct myocardium in both genotypes 3 days after MI, and hyperinnervation was increased in the p75(NTR)-/- mice. By 7 days after ischemia-reperfusion, cardiac sympathetic innervation density returned back to sham-operated levels in both genotypes, indicating that axonal pruning did not require p75(NTR). Prior studies revealed that proNGF is elevated in the damaged left ventricle after ischemia-reperfusion, as is mRNA encoding brain-derived neurotrophic factor (BDNF). ProNGF and BDNF preferentially bind p75(NTR) rather than TrkA on sympathetic neurons. Immunohistochemistry using Bdnf-HA mice confirmed the presence of BDNF or proBDNF in the infarct after ischemia-reperfusion. Thus, at least two p75(NTR) ligands are elevated in the left ventricle after ischemia-reperfusion where they may stimulate p75(NTR)-dependent denervation of peri-infarct myocardium. In contrast, NGF-induced sympathetic hyperinnervation in the distal pen-infarct ventricle is attenuated by p75(NTR). (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:111 / 119
页数:9
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