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表达孤儿核受体Nurr1的皮质-皮质联合神经元的组织与发育

Organization and development of corticocortical associative neurons expressing the orphan nuclear receptor Nurr1.

作者信息

Arimatsu Yasuyoshi, Ishida Mami, Kaneko Takeshi, Ichinose Sachiyo, Omori Akira

机构信息

Cortical Circuits Research Unit, Mitsubishi Kagaku Institute of Life Sciences (MITILS), Tokyo 194-8511, Japan.

出版信息

J Comp Neurol. 2003 Nov 10;466(2):180-96. doi: 10.1002/cne.10875.

DOI:10.1002/cne.10875
PMID:14528447
Abstract

The developmental mechanism that contributes to the highly organized axonal connections within the cerebral cortex is not well understood. This is partly due to the lack of molecular markers specifically expressed in corticocortical associative neurons during the period of circuit formation. We have shown previously that latexin, a carboxypeptidase A inhibitor, is expressed in intrahemispheric corticocortical neurons from the second postnatal week in the rat (Arimatsu et al. [1999] Cereb. Cortex 9:569-576). In the present study, we first demonstrate in the adult rat that the orphan nuclear receptor Nurr1 is coexpressed in latexin-expressing neurons located in layer V, sublayer VIa, and the white matter of the lateral sector of the neocortex, and also in latexin-negative early born neurons in sublayer VIb of the entire neocortex. Virtually all Nurr1-expressing neurons exhibit immunoreactivity for phosphate-activated glutaminase but not for gamma-aminobutyric acid, suggesting that they are glutamatergic-excitatory neurons. By combining Nurr1 immunohistochemistry and 5-bromo-2'-deoxyuridine-birthdating, we then show that Nurr1 is expressed in (early born) subplate neurons and (later born) presumptive latexin-expressing neurons from embryonic day 18 onward. Finally, by combination of Nurr1 immunohistochemistry and retrograde tracing, we show that Nurr1-expressing neurons, including those in sublayer VIb, contribute predominantly to long-range intrahemispheric corticocortical projections. These results raise the possibility that Nurr1 plays a role in the establishment and maintenance of normal corticocortical circuitry and function.

摘要

促成大脑皮质内高度有序轴突连接的发育机制尚未完全明确。部分原因是在回路形成期间,缺乏在皮质-皮质联合神经元中特异性表达的分子标记物。我们之前已经表明,羧肽酶A抑制剂晚近素在大鼠出生后第二周开始在半球内皮质-皮质神经元中表达(有松等人,[1999]《大脑皮质》9:569 - 576)。在本研究中,我们首先在成年大鼠中证明,孤儿核受体Nurr1在位于新皮质外侧区第V层、第VIa亚层和白质中的晚近素表达神经元中共同表达,并且在整个新皮质第VIb亚层中的晚近素阴性早出生神经元中也有表达。几乎所有表达Nurr1的神经元都对磷酸激活谷氨酰胺酶呈免疫反应,但对γ-氨基丁酸不呈免疫反应,这表明它们是谷氨酸能兴奋性神经元。通过结合Nurr1免疫组织化学和5-溴-2'-脱氧尿苷出生标记,我们接着表明,从胚胎第18天起,Nurr1在(早出生的)皮质下板神经元和(晚出生的)推定的晚近素表达神经元中表达。最后,通过Nurr1免疫组织化学和逆行追踪相结合,我们表明,包括第VIb亚层中的那些在内的表达Nurr1的神经元主要参与半球内远距离皮质-皮质投射。这些结果增加了Nurr1在正常皮质-皮质回路和功能的建立与维持中发挥作用的可能性。

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