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在sema3A突变小鼠中,CA1锥体神经元顶端树突近端分支增加。

Increased proximal bifurcation of CA1 pyramidal apical dendrites in sema3A mutant mice.

作者信息

Nakamura Fumio, Ugajin Kozue, Yamashita Naoya, Okada Takako, Uchida Yutaka, Taniguchi Masahiko, Ohshima Toshio, Goshima Yoshio

机构信息

Yokohama City University Graduate School of Medicine, Department of Molecular Pharmacology and Neurobiology, 3-9, Fukuura, Kanazawa-ku, Yokohama, Kanagawa 236-0004, Japan.

出版信息

J Comp Neurol. 2009 Oct 10;516(5):360-75. doi: 10.1002/cne.22125.

Abstract

Semaphorin-3A (Sema3A) is an attractive guidance molecule for cortical apical dendrites. To elucidate the role of Sema3A in hippocampal dendritic formation, we examined the Sema3A expression pattern in the perinatal hippocampal formation and analyzed hippocampal dendrites of the brains from young adult sema3A mutant mice. Sema3A protein was predominantly expressed in the hippocampal plate and the inner marginal zone at the initial period of apical dendritic growth. Neuropilin-1 and plexin-A, the receptor components for Sema3A, were also localized in the same regions. The Golgi impregnation method revealed that in wildtype mice more than 90% of hippocampal CA1 pyramidal neurons extended a single trunk or apical trunks bifurcated in stratum radiatum. Seven percent of the pyramidal neurons showed proximal bifurcation of apical trunks in stratum pyramidale or at the border of the stratum pyramidale and stratum radiatum. In sema3A mutant mice, proximally bifurcated apical dendrites were increased to 32%, while the single apical dendritic pyramidal neurons were decreased. We designate this phenotype in sema3A mutant mice as "proximal bifurcation." In the dissociated culture system, approximately half of the hippocampal neurons from wildtype mice resembled pyramidal neurons, which possess a long, thick, and tapered dendrite. In contrast, only 30% of the neurons from sema3A mutants exhibited pyramidal-like morphology. Proximal bifurcation of CA1 pyramidal neurons was also increased in the mutant mice of p35, an activator of cyclin-dependent kinase 5 (Cdk5). Thus, Sema3A may facilitate the initial growth of CA1 apical dendrites via the activation of p35/Cdk5, which may in turn signal hippocampal development.

摘要

信号素3A(Sema3A)是一种对皮质顶端树突具有吸引作用的导向分子。为了阐明Sema3A在海马树突形成中的作用,我们检测了围产期海马结构中Sema3A的表达模式,并分析了成年早期Sema3A突变小鼠大脑中的海马树突。在顶端树突生长初期,Sema3A蛋白主要在海马板和内边缘区表达。Sema3A的受体成分神经纤毛蛋白-1和丛状蛋白-A也定位于相同区域。高尔基染色法显示,在野生型小鼠中,超过90%的海马CA1锥体神经元伸出单个主干或在辐射层分叉的顶端主干。7%的锥体神经元在锥体层或锥体层与辐射层交界处显示顶端主干近端分叉。在Sema3A突变小鼠中,近端分叉的顶端树突增加到32%,而单个顶端树突锥体神经元减少。我们将Sema3A突变小鼠中的这种表型称为“近端分叉”。在解离培养系统中,野生型小鼠约一半的海马神经元类似于锥体神经元,具有长、粗且逐渐变细的树突。相比之下,Sema3A突变体中只有30%的神经元呈现出类似锥体的形态。在细胞周期蛋白依赖性激酶5(Cdk5)的激活剂p35的突变小鼠中,CA1锥体神经元的近端分叉也增加。因此,Sema3A可能通过激活p35/Cdk5促进CA1顶端树突的初始生长,这反过来可能对海马发育发出信号。

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