Eto Risa, Abe Manami, Hayakawa Natsumi, Kato Hiroyuki, Araki Tsutomu
Department of Neurobiology and Therapeutics, Graduate School and Faculty of Pharmaceutical Sciences, The University of Tokushima, 1-78, Sho-machi, Tokushima, 770-8505, Japan.
Metab Brain Dis. 2008 Dec;23(4):399-409. doi: 10.1007/s11011-008-9103-8. Epub 2008 Sep 4.
We investigated the age-related alterations of calcineurin and Akt1/protein kinase Balpha (Akt1/PKBalpha) immunoreactivity in the mouse hippocampal CA1 sector using immunohistochemistry. Calcineurin and Akt1/PKBalpha immunoreactivity was measured in 2-, 8-, 18-, 40-42- and 50-59-weeks-old animals. Diffuse calcineurin immunoreactivity was evident in pyramidal neurons of the hippocampal CA1 sector of 8-weeks-old mice. Densities of calcineurin immunoreactivity were lowered significantly in the hippocampal CA1 neurons of 2-weeks-old mice. In contrast, densities of calcineurin immunoreactivity were unchanged in the hippocampal CA1 neurons up to 40-42-weeks-old mice. However, densities of calcineurin immunoreactivity were increased significantly in the dendrites and plasma membranes of the hippocampal CA1 neurons of 50-59-weeks-old mice compared to 8-weeks old animals. Akt1/PKBalpha immunoreactivity was slightly detectable in the hippocampal CA1 sector of 8-weeks-old mice. A weak Akt1/PKBalpha immunoreactivity was found in cytoplasm of the hippocampal CA1 neurons and glial cells. Densities of Akt1/PKBalpha immunoreactivity were unchanged in the hippocampal CA1 neurons and glial cells of 2-weeks-old mice. In contrast, densities of Akt1/PKBalpha immunoreactivity were increased significantly in cytoplasm of neurons and glial cells of the hippocampal CA1 sector from 40-42 to 50-59 weeks after birth. The present study indicates that densities of calcineurin immunoreactivity and number of Akt1/PKBalpha immunoreactive cells were increased significantly in the hippocampal CA1 sector during aging processes. Our study also demonstrates that the activation of Akt1/PKBalpha signaling pathway may act defense mechanism against the neuronal dysfunction of the hippocampal CA1 sector caused by the activation of calcineurin signaling pathway during aging processes. These findings suggest that the calcineurin and Akt1/PKBalpha signaling pathway may be important targets for the development of novel therapeutic strategies for protection against age-related neurodegeneration.
我们采用免疫组织化学方法,研究了小鼠海马CA1区中钙调神经磷酸酶和Akt1/蛋白激酶Bα(Akt1/PKBα)免疫反应性随年龄的变化。在2周龄、8周龄、18周龄、40 - 42周龄和50 - 59周龄的动物中测量了钙调神经磷酸酶和Akt1/PKBα的免疫反应性。在8周龄小鼠海马CA1区的锥体神经元中,弥漫性钙调神经磷酸酶免疫反应性明显。在2周龄小鼠海马CA1神经元中,钙调神经磷酸酶免疫反应性密度显著降低。相比之下,在40 - 42周龄小鼠的海马CA1神经元中,钙调神经磷酸酶免疫反应性密度没有变化。然而,与8周龄动物相比,50 - 59周龄小鼠海马CA1神经元的树突和质膜中钙调神经磷酸酶免疫反应性密度显著增加。在8周龄小鼠海马CA1区可略微检测到Akt1/PKBα免疫反应性。在海马CA1神经元和神经胶质细胞的细胞质中发现微弱的Akt1/PKBα免疫反应性。在2周龄小鼠的海马CA1神经元和神经胶质细胞中,Akt1/PKBα免疫反应性密度没有变化。相比之下,出生后40 - 42周至50 - 59周期间,海马CA1区神经元和神经胶质细胞细胞质中Akt1/PKBα免疫反应性密度显著增加。本研究表明,在衰老过程中,海马CA1区钙调神经磷酸酶免疫反应性密度和Akt1/PKBα免疫反应性细胞数量显著增加。我们的研究还表明,Akt1/PKBα信号通路的激活可能作为一种防御机制,抵御衰老过程中由钙调神经磷酸酶信号通路激活引起的海马CA1区神经元功能障碍。这些发现表明,钙调神经磷酸酶和Akt1/PKBα信号通路可能是开发新型治疗策略以预防年龄相关性神经退行性变的重要靶点。