Kawaguchi-Manabe Haruko, Ieda Masaki, Kimura Kensuke, Manabe Tomohiro, Miyatake Satoru, Kanazawa Hideaki, Kawakami Takashi, Ogawa Satoshi, Suematsu Makoto, Fukuda Keiichi
Department of Regenerative Medicine and Advanced Cardiac Therapeutics, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan.
Life Sci. 2007 Jul 12;81(5):385-92. doi: 10.1016/j.lfs.2007.05.024. Epub 2007 Jun 16.
The neurotrophin family plays pivotal roles in the development of the nervous system. Recently, the role of the neurotrophin in non-neural tissue has been extensively investigated. Among them, neurotrophin-3 and its receptor TrkC are critical for embryonic heart development, though little is known about neurotrophin-3/TrkC function in adult heart. Moreover, the expressions of other neurotrophin and Trk families in the cardiovascular system have not been fully determined. In adult and neonatal rats, only TrkC mRNA was expressed more abundantly in heart than aorta among the neurotrophin receptors, while all neurotrophins were equally expressed in the cardiovascular system. Immunohistochemistry confirmed the protein expressions of neurotrophin-3/TrkC in rat ventricles. In primary-cultured rat cardiomyocytes, neurotrophin-3 strongly activated p38 mitogen-activated protein kinase, extracellular signal-regulated kinase 1/2, and Jun N-terminal kinase pathways in Western blot analysis. In Northern blot analysis, neurotrophin-3 strongly increased mRNA expressions of cardiac hypertrophic markers (skeletal alpha-actin and atrial natriuretic peptide) in cardiomocytes. [(3)H]-phenylalanine uptake into cardiomyocytes, myofilament reorganization, and cardiomyocyte size were also augmented with neurotrophin-3 stimulation, indicating that neurotrophin-3 is a novel cardiac hypertrophic factor. Unexpectedly, neurotrophin-3 was downregulated in cardiac hypertrophy induced by pressure overload (in vivo), and in cardiomyocyte hypertrophy evoked by endothelin-1 stimulation (in vitro). Interestingly, the cell size and BNP mRNA expression level (markers of hypertrophy) were greater in cardiomyocytes treated with both neurotrophin-3 and endothelin-1 than in those stimulated with endothelin-1 alone. These findings demonstrate that neurotrophin-3 is a unique hypertrophic factor, which is paradoxically downregulated in cardiac hypertrophy and might counteract hypertrophic change.
神经营养因子家族在神经系统发育中发挥着关键作用。最近,神经营养因子在非神经组织中的作用得到了广泛研究。其中,神经营养因子-3及其受体TrkC对胚胎心脏发育至关重要,然而关于神经营养因子-3/TrkC在成年心脏中的功能却知之甚少。此外,其他神经营养因子和Trk家族在心血管系统中的表达尚未完全明确。在成年和新生大鼠中,在神经营养因子受体中,只有TrkC mRNA在心脏中的表达比在主动脉中更丰富,而所有神经营养因子在心血管系统中表达水平相当。免疫组织化学证实了神经营养因子-3/TrkC在大鼠心室中的蛋白表达。在原代培养的大鼠心肌细胞中,蛋白质印迹分析显示神经营养因子-3强烈激活p38丝裂原活化蛋白激酶、细胞外信号调节激酶1/2和Jun N末端激酶信号通路。在Northern印迹分析中,神经营养因子-3强烈增加心肌细胞中心脏肥厚标志物(骨骼肌α-肌动蛋白和心钠素)的mRNA表达。神经营养因子-3刺激还增强了[³H]-苯丙氨酸摄取到心肌细胞中的能力、肌丝重组以及心肌细胞大小,表明神经营养因子-3是一种新型的心脏肥厚因子。出乎意料的是,在压力超负荷诱导的心脏肥厚(体内)以及内皮素-1刺激引起的心肌细胞肥大(体外)中,神经营养因子-3表达下调。有趣的是,同时用神经营养因子-3和内皮素-1处理的心肌细胞的细胞大小和BNP mRNA表达水平(肥厚标志物)比单独用内皮素-1刺激的心肌细胞更大。这些发现表明神经营养因子-3是一种独特的肥厚因子,在心脏肥厚中反常地下调,可能会抵消肥厚性变化。