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nNOS基因敲除(-/-)小鼠大脑皮质和海马区钙结合蛋白(钙结合蛋白-D28k、钙视网膜蛋白和小白蛋白)表达的免疫组织化学研究

Immunohistochemical study on the expression of calcium binding proteins (calbindin-D28k, calretinin, and parvalbumin) in the cerebral cortex and in the hippocampal region of nNOS knock-out(-/-) mice.

作者信息

Cho Yu Jin, Lee Jae Chul, Kang Bong Gu, An Jaeyeol, Song Hyeon Suk, Son Onju, Nam Do-Hyun, Cha Choong Ik, Joo Kyeung Min

机构信息

Department of Anatomy, College of Medicine, Seoul National University, Seoul, Korea.

出版信息

Anat Cell Biol. 2011 Jun;44(2):106-15. doi: 10.5115/acb.2011.44.2.106. Epub 2011 Jun 30.

Abstract

Nitric oxide (NO) modulates the activities of various channels and receptors to participate in the regulation of neuronal intracellular Ca(2+) levels. Ca(2+) binding protein (CaBP) expression may also be altered by NO. Accordingly, we examined expression changes in calbindin-D28k, calretinin, and parvalbumin in the cerebral cortex and hippocampal region of neuronal NO synthase knockout(-/-) (nNOS(-/-)) mice using immunohistochemistry. For the first time, we demonstrate that the expression of CaBPs is specifically altered in the cerebral cortex and hippocampal region of nNOS(-/-) mice and that their expression changed according to neuronal type. As changes in CaBP expression can influence temporal and spatial intracellular Ca(2+) levels, it appears that NO may be involved in various functions, such as modulating neuronal Ca(2+) homeostasis, regulating synaptic transmission, and neuroprotection, by influencing the expression of CaBPs. Therefore, these results suggest another mechanism by which NO participates in the regulation of neuronal Ca(2+) homeostasis. However, the exact mechanisms of this regulation and its functional significance require further investigation.

摘要

一氧化氮(NO)调节各种通道和受体的活性,参与神经元细胞内Ca(2+)水平的调节。Ca(2+)结合蛋白(CaBP)的表达也可能受NO影响而改变。因此,我们采用免疫组化方法检测了神经元型一氧化氮合酶基因敲除(-/-)(nNOS(-/-))小鼠大脑皮质和海马区中钙结合蛋白-D28k、钙视网膜蛋白和小白蛋白的表达变化。我们首次证明,nNOS(-/-)小鼠大脑皮质和海马区中CaBPs的表达发生特异性改变,且其表达随神经元类型而变化。由于CaBP表达的变化会影响细胞内Ca(2+)水平的时空变化,因此NO似乎可能通过影响CaBPs的表达参与多种功能,如调节神经元Ca(2+)稳态、调节突触传递和神经保护。因此,这些结果提示了NO参与神经元Ca(2+)稳态调节的另一种机制。然而,这种调节的确切机制及其功能意义仍需进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e39b/3145839/718e7aced23a/acb-44-106-g001.jpg

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