Banisadr Ghazal, Fontanges Philippe, Haour France, Kitabgi Patrick, Rostène William, Mélik Parsadaniantz Stéphane
Imagerie Cellulaire des Neurorécepteurs et Physiopathologie Neuroendocrinienne, INSERM U. 339; Hôpital Saint-Antoine, 184 rue du Faubourg Saint-Antoine, 75571 Paris Cedex 12, France.
Eur J Neurosci. 2002 Nov;16(9):1661-71. doi: 10.1046/j.1460-9568.2002.02237.x.
Accumulating evidence supports a role of chemokines and their receptors in brain function. Up to now scarce evidence has been given of the neuroanatomical distribution of chemokine receptors. Although it is widely accepted that chemokine receptors are present on glial cells, especially in pathological conditions, it remains unclear whether they are constitutively present in normal rat brain and whether neurons have the potential to express such chemokine receptors. CXCR4, a G protein-coupled receptor for the chemokine stromal cell-derived factor-1 (SDF-1/CXCL12) was reported to have possible implications in brain development and AIDS-related dementia. By dual immunohistochemistry on brain sections, we clearly demonstrate that CXCR4 is constitutively expressed in adult rat brain, in glial cells (astrocytes, microglia but not oligodendrocytes) as well as in neurons. Neuronal expression of CXCR4 is mainly found in cerebral cortex, caudate putamen, globus pallidus, substantia innominata, supraoptic and paraventricular hypothalamic nuclei, ventromedial thalamic nucleus and substantia nigra. Using confocal microscopy, a differential distribution of CXCR4 in neuronal perikarya and dendrites can be observed according to the brain structure. Furthermore, this work demonstrates for the first time the coexistence of a chemokine receptor with classical neurotransmitters. A localization of CXCR4 is thus observed in neuronal cell bodies expressing choline acetyltransferase-immunoreactivity in the caudate putamen and substantia innominata, as well as in tyrosine hydroxylase-positive neurons in the substantia nigra pars compacta. In conclusion, the constitutive neuronal CXCR4 expression suggests that SDF-1/CXCL12 could be involved in neuronal communication and possibly linked up with cholinergic and dopaminergic neurotransmission and related disorders.
越来越多的证据支持趋化因子及其受体在脑功能中发挥作用。到目前为止,关于趋化因子受体的神经解剖学分布的证据很少。尽管人们普遍认为趋化因子受体存在于神经胶质细胞上,尤其是在病理条件下,但它们是否在正常大鼠脑中持续存在,以及神经元是否有表达此类趋化因子受体的潜力仍不清楚。据报道,CXCR4是趋化因子基质细胞衍生因子-1(SDF-1/CXCL12)的G蛋白偶联受体,可能与脑发育和艾滋病相关痴呆有关。通过对脑切片进行双重免疫组织化学,我们清楚地证明CXCR4在成年大鼠脑中持续表达,存在于神经胶质细胞(星形胶质细胞、小胶质细胞,但少突胶质细胞中没有)以及神经元中。CXCR4的神经元表达主要见于大脑皮层、尾状壳核、苍白球、无名质、视上核和室旁下丘脑核、丘脑腹内侧核和黑质。使用共聚焦显微镜,可以根据脑结构观察到CXCR4在神经元胞体和树突中的差异分布。此外,这项工作首次证明了趋化因子受体与经典神经递质共存。因此,在尾状壳核和无名质中表达胆碱乙酰转移酶免疫反应性的神经元细胞体中,以及在黑质致密部的酪氨酸羟化酶阳性神经元中,观察到了CXCR4的定位。总之,CXCR4在神经元中的持续表达表明SDF-1/CXCL12可能参与神经元通讯,并可能与胆碱能和多巴胺能神经传递及相关疾病有关。