Eghbal-Ahmadi M, Hatalski C G, Lovenberg T W, Avishai-Eliner S, Chalmers D T, Baram T Z
Department of Anatomy and Neurobiology, University of California, Irvine 92697-4475, USA.
Brain Res Dev Brain Res. 1998 Apr 17;107(1):81-90. doi: 10.1016/s0165-3806(98)00002-9.
Corticotropin releasing factor (CRF) activates two known receptor types, CRF1, and CRF2. In the adult rat brain, CRF2 has a distinct distribution pattern, suggesting that it may mediate functions exclusive of CRF1. The goal of this study was to determine the age-dependent distribution of CRF2-messenger RNA (CRF2-mRNA) in the rat brain. Brains from rats sacrificed under stress-free conditions on fetal days (F) 15, 16, 17 and 19, and postnatal days 1, 3, 5, 7, 9, 12, 15, 25, 49, and 90 (adult) were analyzed using semiquantitative in situ hybridization histochemistry. The onset and distribution of CRF2-mRNA in the developing rat brain revealed important differences from the adult expression pattern: earliest expression of CRF2-mRNA was observed in the ventromedial hypothalamus (VMH) on F16. High levels of CRF2-mRNA were present in the fronto-parietal cortex in the fetal and early postnatal brain but not later. Conversely, no CRF2-mRNA was detectable in the ventroposterior (lateral and medial) thalamic nuclei prior to postnatal day 7. Distinct developmental profiles of CRF2-mRNA were also observed in the lateral septum, medial, basal and cortical amygdala nuclei, and in several hippocampal fields. In conclusion, CRF2 is expressed in the hypothalamus on F16, prior to the detection of CRF itself in the paraventricular nucleus. The differential levels and distributions of CRF2-mRNA in hypothalamic and limbic brain regions indicate a precise regulation of this receptor's expression during development, as shown for CRF1. Regulation of the levels of CRF2 may modulate the effects of CRF (and related ligands) on target neurons, consistent with differential maturation of the functions mediated by this receptor.
促肾上腺皮质激素释放因子(CRF)可激活两种已知的受体类型,即CRF1和CRF2。在成年大鼠脑中,CRF2具有独特的分布模式,这表明它可能介导一些CRF1所不具备的功能。本研究的目的是确定大鼠脑中CRF2信使核糖核酸(CRF2-mRNA)随年龄的分布情况。使用半定量原位杂交组织化学方法分析了在胎儿期第15、16、17和19天以及出生后第1、3、5、7、9、12、15、25、49和90天(成年)在无应激条件下处死的大鼠的脑。发育中大鼠脑内CRF2-mRNA的起始和分布与成年表达模式存在重要差异:在胎儿期第16天,促肾上腺皮质激素释放因子2信使核糖核酸最早在腹内侧下丘脑(VMH)表达。在胎儿期和出生后早期的脑内,额顶叶皮质中存在高水平的CRF2-mRNA,但后期则没有。相反,在出生后第7天之前,腹后(外侧和内侧)丘脑核中未检测到CRF2-mRNA。在外侧隔核、内侧、基底和皮质杏仁核以及几个海马区域也观察到了CRF2-mRNA不同的发育情况。总之,在室旁核中检测到CRF之前,CRF2在胎儿期第16天就在下丘脑表达。下丘脑和边缘脑区中CRF2-mRNA水平和分布的差异表明,该受体在发育过程中的表达受到精确调控,CRF1也是如此。CRF2水平的调节可能会调节CRF(及相关配体)对靶神经元的作用,这与该受体介导的功能的不同成熟情况一致。