Sedaghat K, Shen P-J, Finkelstein D I, Henderson J M, Gundlach A L
Howard Florey Institute, The University of Melbourne, Victoria 3010, Australia.
Neuroscience. 2008 Oct 2;156(2):319-33. doi: 10.1016/j.neuroscience.2008.07.029. Epub 2008 Jul 25.
Leucine-rich repeat-containing G-protein-coupled receptor 8 (LGR8; also classified as relaxin family peptide 2 receptor; RXFP2) has been identified as a cognate receptor for the peptide hormone, insulin-like peptide 3 (INSL3) and INSL3-LGR8 signaling plays an essential role in testis descent and germ cell development in human and rodents. Lgr8 mRNA has been detected in human tissues including testis, kidney and brain, but its regional and cellular distribution in these tissues in human or other species is largely unknown. In an initial step to elucidate the physiological function of a putative INSL3-LGR8 system in rat brain, the localization of Lgr8 mRNA was investigated using in situ hybridization histochemistry, revealing a discrete distribution in forebrain, with expression highly enriched in the thalamus. High densities were detected in the parafascicular nucleus (Pf), the dorsolateral, ventrolateral and posterior thalamic nuclei, and in the medial habenula. Lgr8 transcripts were also detected in frontal and motor cortices. The comparative distribution of LGR8 (receptor protein) was examined by autoradiography of [125I]-human INSL3 binding sites, with high densities detected in the thalamus, especially in Pf, and in the entire striatum--the caudate putamen (CPmicro), islands of Calleja, olfactory tubercle, nucleus accumbens--with lower levels in distinct layers of cerebral cortex. Notably, these areas also receive dopaminergic projections. These findings demonstrate the existence of LGR8 in neuronal soma in the thalamus and axons/terminals in thalamic target areas such as the striatum and frontal cortex. LGR8 was also detected throughout the medial habenula-fasciculus retroflexus-interpeduncular nucleus pathway, further indicating that the receptor is transported from mRNA-expressing soma to remote axonal/terminal sites. These findings suggest the existence of a broadly distributed LGR8 signaling system in the rat involved in sensorimotor, limbic and cognitive functions. Further studies are now required to elucidate the precise function of LGR8, under normal and pathological conditions, as importantly, several of the equivalent receptor-positive areas in human brain are part of the pathology of neurodegenerative conditions including Parkinson's disease.
富含亮氨酸重复序列的G蛋白偶联受体8(LGR8;也被归类为松弛素家族肽2受体;RXFP2)已被确定为肽激素胰岛素样肽3(INSL3)的同源受体,并且INSL3-LGR8信号传导在人类和啮齿动物的睾丸下降和生殖细胞发育中起着至关重要的作用。已在包括睾丸、肾脏和大脑在内的人体组织中检测到Lgr8 mRNA,但其在人类或其他物种这些组织中的区域和细胞分布在很大程度上尚不清楚。作为阐明大鼠脑中假定的INSL3-LGR8系统生理功能的第一步,使用原位杂交组织化学研究了Lgr8 mRNA的定位,结果显示其在前脑呈离散分布,在丘脑中表达高度富集。在束旁核(Pf)、背外侧、腹外侧和丘脑后核以及内侧缰核中检测到高密度表达。在额叶和运动皮层中也检测到了Lgr8转录本。通过对[125I]-人INSL3结合位点进行放射自显影检查了LGR8(受体蛋白)的比较分布,在丘脑中检测到高密度,尤其是在Pf以及整个纹状体——尾状壳核(CPmicro)、卡勒哈岛、嗅结节、伏隔核——在大脑皮层的不同层中水平较低。值得注意的是,这些区域也接受多巴胺能投射。这些发现证明了LGR8存在于丘脑的神经元胞体以及丘脑靶区域如纹状体和额叶皮层的轴突/终末中。在整个内侧缰核-后屈束-脚间核通路中也检测到了LGR8,这进一步表明该受体从表达mRNA的胞体运输到远端轴突/终末位点。这些发现表明在大鼠中存在一个广泛分布的LGR8信号系统,参与感觉运动、边缘和认知功能。现在需要进一步研究以阐明LGR8在正常和病理条件下的确切功能,同样重要的是,人类大脑中几个等效的受体阳性区域是包括帕金森病在内的神经退行性疾病病理学病变的一部分。