Shiota Jun, Ishikawa Mitsuru, Sakagami Hiroyuki, Tsuda Masaaki, Baraban Jay M, Tabuchi Akiko
Department of Biological Chemistry, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama City, Japan.
J Neurochem. 2006 Sep;98(6):1778-88. doi: 10.1111/j.1471-4159.2006.03992.x.
The dynamic changes in dendritic morphology displayed by developing and mature neurons have stimulated interest in deciphering the signaling pathways involved. Recent studies have identified megakaryocytic acute leukemia (MAL), a serum response factor (SRF) co-activator, as a key component of a signaling pathway linking changes in the actin cytoskeleton to SRF-mediated transcription. To help define the role of this pathway in regulating dendritic morphology, we have characterized the pattern of MAL expression in the developing and adult brain, and have examined its role in regulating dendritic morphology in cultured cortical neurons. In histological studies of mouse brain, we found prominent expression of MAL in neurons in adult hippocampus and cerebral cortex. MAL immunostaining revealed localization of this protein in neuronal cell bodies and apical dendrites. During development, an increase in MAL expression occurs during the second post-natal week. Expression of dominant negative MAL constructs or MAL siRNA in cortical neurons grown in primary culture reduces the number of dendritic processes and decreases the basal level of SRF-mediated transcription. Taken together, these findings indicate that the MAL-SRF signaling pathway plays a key role in regulating dendritic morphology.
发育中和成熟神经元所呈现的树突形态的动态变化激发了人们对解读其中涉及的信号通路的兴趣。最近的研究已确定巨核细胞急性白血病(MAL),一种血清反应因子(SRF)共激活因子,是将肌动蛋白细胞骨架变化与SRF介导的转录联系起来的信号通路的关键组成部分。为了帮助确定该通路在调节树突形态中的作用,我们已对发育中和成年大脑中MAL的表达模式进行了表征,并研究了其在调节培养的皮质神经元树突形态中的作用。在小鼠脑的组织学研究中,我们发现成年海马体和大脑皮质中的神经元中有显著的MAL表达。MAL免疫染色显示该蛋白定位于神经元细胞体和顶端树突中。在发育过程中,出生后第二周MAL表达增加。在原代培养中生长的皮质神经元中表达显性负性MAL构建体或MAL小干扰RNA会减少树突分支的数量,并降低SRF介导的转录的基础水平。综上所述,这些发现表明MAL-SRF信号通路在调节树突形态中起关键作用。