Differential expression of the regulator of G protein signaling RGS9 protein in nociceptive pathways of different age rats

Ki Jun Kim, Kumi Moriyama, Kyung Ream Han, Manohar Sharma, Xiaokang Han, Guo-xi Xie, Pamela Pierce Palmer
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引用次数: 17

Abstract

Regulators of G protein signaling (RGS) proteins are GTPase-activating proteins which act as modulators of G-protein-coupled receptors. RGS9 has two alternative splicing variants. RGS9-1 is expressed in the retina. RGS9-2 is expressed in the brain, especially abundant in the striatum. It is believed to be an essential regulatory component of dopamine and opioid signaling. In this study, we compared the expression of RGS9 proteins in the nervous system of different age groups of rats employing immunocytochemistry. In both 3-week- and 1-year-old rats, RGS9 is expressed abundantly in caudate–putamen, nucleus accumbens, and olfactory tubercle. It is also expressed abundantly in the ventral horn of the spinal cord and the dorsal root ganglion (DRG) cells. Quantitative analysis showed that the intensities of RGS9 expression in 1-year-old rats are higher than those in the 3-week-old rats in caudate–putamen, nucleus accumbens, olfactory tubercle, periaqueductal gray, and gray matter of the spinal cord. In contrast, in thalamic nuclei and locus coeruleus, the intensities of RGS9 immunostaining in 3-week-old rats are higher than in 1-year-old rats. In DRG cells, there is no significant difference between the two age groups. These data suggest that RGS9 is differentially expressed with age. Such differential expression may play an important role in neuronal differentiation and development as well as in neuronal function, such as dopamine and opioid signaling.

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G蛋白信号通路调控因子RGS9蛋白在不同年龄大鼠痛觉通路中的差异表达
G蛋白信号(RGS)蛋白的调节因子是gtpase激活蛋白,作为G蛋白偶联受体的调节剂。RGS9有两个可选的剪接变体。RGS9-1在视网膜中表达。RGS9-2在大脑中表达,尤其在纹状体中表达丰富。它被认为是多巴胺和阿片信号传导的重要调节成分。本研究采用免疫细胞化学方法比较了RGS9蛋白在不同年龄组大鼠神经系统中的表达情况。在3周龄和1岁大鼠中,RGS9在尾壳核、伏隔核和嗅结节中大量表达。它也在脊髓前角和背根神经节(DRG)细胞中大量表达。定量分析显示,1岁大鼠尾壳核、伏隔核、嗅结节、导水管周围灰质和脊髓灰质中RGS9的表达强度高于3周龄大鼠。相比之下,3周龄大鼠丘脑核和蓝斑区RGS9免疫染色强度高于1岁大鼠。在DRG细胞方面,两组间无显著差异。这些数据表明RGS9的表达随年龄的增长而不同。这种差异表达可能在神经元分化和发育以及神经元功能中发挥重要作用,如多巴胺和阿片信号传导。
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