From the, Laboratory of Behavioral Neurobiology, (GQC, ADC, OK, GG, SFL), The Rockefeller University, New York, New York.
School of Medicine, (DSSKB), The University of Pittsburgh, Pittsburgh, Pennsylvania.
Alcohol Clin Exp Res. 2020 Apr;44(4):866-879. doi: 10.1111/acer.14296. Epub 2020 Feb 26.
Prenatal exposure to ethanol (EtOH) has lasting effects on neuropeptide and neuroimmune systems in the brain alongside detrimental alcohol-related behaviors. At low-to-moderate doses, prenatal EtOH stimulates neurogenesis in lateral hypothalamus (LH) and increases neurons that express the orexigenic peptides hypocretin/orexin (Hcrt/OX) and melanin-concentrating hormone (MCH), and the proinflammatory chemokine CCL2, which through its receptor CCR2 stimulates cell differentiation and movement. Our recent studies demonstrated that CCL2 and CCR2 colocalize with MCH neurons and are involved in EtOH's stimulatory effect on their development but show no relation to Hcrt/OX. Here, we investigated another chemokine, CXCL12, and its receptor, CXCR4, which promote neurogenesis and neuroprogenitor cell proliferation, to determine if they also exhibit peptide specificity in their response to EtOH exposure.
Pregnant rats were intraorally administered a moderate dose of EtOH (2 g/kg/d) from embryonic day 10 (E10) to E15. Their embryos and postnatal offspring were examined using real-time quantitative PCR and immunofluorescence histochemistry, to determine if EtOH affects CXCL12 and CXCR4 and the colocalization of CXCR4 with Hcrt/OX and MCH neurons in the LH and with radial glia neuroprogenitor cells in the hypothalamic neuroepithelium (NEP).
Prenatal EtOH strongly stimulated CXCL12 and CXCR4 in LH neurons of embryos and postnatal offspring. This stimulation was significantly stronger in Hcrt/OX than MCH neurons in LH and also occurred in radial glia neuroprogenitor cells dense in the NEP. These effects were sexually dimorphic, consistently stronger in females than males.
While showing prenatal EtOH exposure to have a sexually dimorphic, stimulatory effect on CXCL12 and CXCR4 in LH similar to CCL2 and its receptor, these results reveal their distinct relationship to the peptide neurons, with the former closely related to Hcrt/OX and the latter to MCH, and they link EtOH's actions in LH to a stimulatory effect on neuroprogenitor cells in the NEP.
产前暴露于乙醇(EtOH)会对大脑中的神经肽和神经免疫系统产生持久影响,同时还会导致与酒精相关的有害行为。在低至中等剂量下,产前 EtOH 会刺激外侧下丘脑(LH)中的神经发生,并增加表达食欲肽(orexigenic peptides)下丘脑泌素/食欲素(Hcrt/OX)和黑色素浓缩激素(melanin-concentrating hormone,MCH)的神经元,以及促炎趋化因子 CCL2,其通过受体 CCR2 刺激细胞分化和迁移。我们最近的研究表明,CCL2 和 CCR2 与 MCH 神经元共定位,并参与 EtOH 对其发育的刺激作用,但与 Hcrt/OX 无关。在这里,我们研究了另一种趋化因子 CXCL12 及其受体 CXCR4,它们促进神经发生和神经祖细胞增殖,以确定它们在对 EtOH 暴露的反应中是否也表现出肽特异性。
从胚胎第 10 天(E10)到 E15 期间,给怀孕的大鼠口服给予中等剂量的 EtOH(2 g/kg/d)。使用实时定量 PCR 和免疫荧光组织化学技术检查它们的胚胎和产后后代,以确定 EtOH 是否影响 CXCL12 和 CXCR4,以及 CXCR4 与 LH 中的 Hcrt/OX 和 MCH 神经元以及下丘脑神经上皮(NEP)中富含的放射状胶质神经祖细胞的共定位。
产前 EtOH 强烈刺激 LH 神经元中的 CXCL12 和 CXCR4,在 LH 中的 Hcrt/OX 神经元中比 MCH 神经元的刺激作用更强,并且也发生在 NEP 中富含的放射状胶质神经祖细胞中。这些作用具有性别二态性,在雌性中比雄性更强。
虽然产前 EtOH 暴露对 LH 中的 CXCL12 和 CXCR4 具有性别二态性刺激作用,类似于 CCL2 和其受体,但这些结果揭示了它们与肽神经元的不同关系,前者与 Hcrt/OX 密切相关,后者与 MCH 相关,它们将 EtOH 在 LH 中的作用与对 NEP 中神经祖细胞的刺激作用联系起来。