Sollars P J, Kimble D P, Pickard G E
Department of Psychiatry, University of Pennsylvania School of Medicine, Philadelphia.
J Neurosci. 1995 Mar;15(3 Pt 2):2109-22. doi: 10.1523/JNEUROSCI.15-03-02109.1995.
The suprachiasmatic nucleus (SCN) of the anterior hypothalamus (AH) is a circadian oscillator and an important component of the mammalian circadian system. To determine whether the SCN is the dominant circadian pacemaker responsible for generating a species-typical characteristic of circadian rhythms [i.e., period length (tau)], neural transplantation was conducted using fetal AH donors of different species and SCN-lesioned (SCNx) hosts. The circadian behavior of each of the three donor species is clearly distinguishable by its species-typical tau. The extent of SCN pacemaker autonomy was assessed by noting whether the period of the restored circadian rhythm following heterograft transplantation was characteristic of the donor or the host, or whether an atypical circadian period was established. Hamsters rendered arhythmic by SCN ablation were implanted with AH tissue from fetal hamsters (E13-E14, homograft controls) or fetal mice or rats (E15-E17). The AH homografts restored circadian activity rhythms with a tau similar to that of intact hamsters, and fetal mouse AH heterografts restored circadian rhythmicity with a tau similar to that of the donor mouse strain. However, fetal rat AH tissue implanted into SCNx hamsters renewed circadian rhythmicity with a period significantly shorter than either the species-typical tau of the rat donor or the hamster host. In both the mouse and rat AH heterograft experiments, immunocytochemical analysis performed with species-specific monoclonal antibodies revealed extensive fiber outgrowth from the implant into the host hypothalamus, evident up to 7 months postimplantation. The rat implants were consistently larger, more fully vascularized and exhibited less necrosis than the implanted mouse tissue. The histological appearance of the grafts, thus, provides no explantation for the difference in efficacy of the grafts to restore species-typical behavior. However, several interpretations are considered that are consistent with the combined behavioral results observed.
下丘脑前部(AH)的视交叉上核(SCN)是一个昼夜节律振荡器,也是哺乳动物昼夜节律系统的重要组成部分。为了确定SCN是否是负责产生昼夜节律的物种典型特征[即周期长度(tau)]的主要昼夜节律起搏器,使用不同物种的胎儿AH供体和SCN损伤(SCNx)宿主进行了神经移植。三种供体物种各自的昼夜节律行为都因其物种典型的tau而明显可区分。通过观察异种移植后恢复的昼夜节律的周期是供体还是宿主的特征,或者是否建立了非典型的昼夜周期,来评估SCN起搏器的自主程度。通过SCN切除而变得无节律的仓鼠被植入来自胎儿仓鼠(E13 - E14,同种移植对照)或胎儿小鼠或大鼠(E15 - E17)的AH组织。AH同种移植恢复了昼夜活动节律,其tau与完整仓鼠的相似,而胎儿小鼠AH异种移植恢复了昼夜节律性,其tau与供体小鼠品系的相似。然而,植入SCNx仓鼠的胎儿大鼠AH组织恢复了昼夜节律性,但其周期明显短于大鼠供体或仓鼠宿主的物种典型tau。在小鼠和大鼠AH异种移植实验中,用物种特异性单克隆抗体进行的免疫细胞化学分析显示,植入物中有大量纤维长入宿主下丘脑,在植入后7个月仍很明显。大鼠植入物始终比植入的小鼠组织更大、血管化更充分且坏死更少。因此,移植物的组织学外观无法解释移植物恢复物种典型行为的效果差异。然而,考虑了几种与观察到的综合行为结果一致的解释。