Department of Behavioral Neuroscience, Oregon Health and Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239, USA.
Brain Res. 2010 Mar 10;1319:33-43. doi: 10.1016/j.brainres.2010.01.003. Epub 2010 Jan 11.
Urocortin 1 (Ucn 1) is an endogenous corticotropin releasing factor (CRF)-related peptide. Ucn 1 is most highly expressed in the perioculomotor urocortin containing neurons (pIIIu), previously known as the non-preganglionic Edinger-Westphal nucleus (npEW). Various studies indicate that these cells are involved in stress adaptation and the regulation of ethanol (EtOH) intake. However, the developmental trajectory of these neurons remained unexamined. Expression of the cocaine- and amphetamine-regulated transcript (CART), which co-localizes with Ucn 1 in the perioculomotor area (pIII) has been examined prenatally, but not postnatally. The goal of the current study was to characterize the ontogenetic profile of Ucn 1 and CART during postnatal development in C57BL/6J (B6) mice. B6 mice were bred, and brains were collected at postnatal days (PND) 1, 4, 8, 12, 16, 24 and 45. Brightfield immunohistochemical staining for Ucn 1 and CART showed that Ucn 1-immunoreactivity (ir) was absent at PND 1, while CART-ir was already apparent in pIIIu at birth, a finding indicating that although the pIIIu neurons have already migrated to their adult position, Ucn 1 expression is triggered in them at later postnatal stages. Ucn 1-ir gradually increased with age, approaching adult levels at PND 16. This developmental profile was confirmed by double-immunofluorescence, which showed that Ucn 1 was absent in CART-positive cells of pIII at PND 4 and that Ucn 1 and CART are strongly but not completely co-localized in pIII at PND 24. Quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) analysis confirmed that Ucn 1 mRNA levels are significantly lower at PND 4 and PND 12 than in adult animals. The lack of brain Ucn 1 immunoreactivity at birth and the gradual postnatal increase in Ucn 1 in pIIIu suggests that this peptide plays a greater behavioral role in adulthood than during the early postnatal development of an organism.
孤啡肽 1(Ucn1)是一种内源性促肾上腺皮质激素释放因子(CRF)相关肽。Ucn1 在眶周含 Ucn1 的神经元(pIIIu)中表达最高,这些神经元之前被称为非节前 Edinger-Westphal 核(npEW)。各种研究表明,这些细胞参与应激适应和乙醇(EtOH)摄入的调节。然而,这些神经元的发育轨迹仍未被研究。可卡因和安非他命调节的转录本(CART)的表达与 pIII 中的 Ucn1 共定位,在产前已经被研究过,但在产后没有被研究过。本研究的目的是描述 C57BL/6J(B6)小鼠出生后发育过程中 Ucn1 和 CART 的发育特征。B6 小鼠繁殖,在出生后第 1、4、8、12、16、24 和 45 天收集大脑。Ucn1 和 CART 的明场免疫组织化学染色显示,Ucn1 免疫反应(ir)在出生时不存在,而 CART-ir 在 pIIIu 中已经存在,这一发现表明,尽管 pIIIu 神经元已经迁移到它们的成年位置,但 Ucn1 的表达是在它们出生后更晚的阶段被触发的。Ucn1-ir 随着年龄的增长逐渐增加,在出生后第 16 天接近成年水平。这一发育特征通过双重免疫荧光得到证实,该研究表明,在出生后第 4 天,Ucn1 不存在于 pIII 中的 CART 阳性细胞中,而在出生后第 24 天,Ucn1 和 CART 在 pIII 中强烈但不完全共定位。定量逆转录聚合酶链反应(qRT-PCR)分析证实,Ucn1 mRNA 水平在出生后第 4 天和第 12 天明显低于成年动物。出生时大脑中缺乏 Ucn1 免疫反应和 pIIIu 中 Ucn1 的逐渐增加表明,这种肽在成年期比在生物体的早期出生后发育中发挥更大的行为作用。