Angka Heather E, Geddes Allison J, Kablar Boris
Department of Anatomy and Neurobiology, Dalhousie University, Sir Charles Tupper Building, Halifax, Nova Scotia.
Dev Dyn. 2008 Nov;237(11):3169-78. doi: 10.1002/dvdy.21727.
Glial cell line-derived neurotrophic factor (GDNF) is known as a potent survival factor for neurons in vitro and in vivo. The current study investigated the effects of a single in utero injection with GDNF in both wild-type and Myf5-/-:MyoD-/- embryos. The embryos in the latter group, denoted double mutants (DM), do not contain skeletal muscle and associated neurotrophic factors due to lack of myogenesis and, therefore, neurons of the central and peripheral nervous system undergo excessively occurring programmed cell death (EPCD). We found that treatment with GDNF had no effect on wild type neuronal numbers in any of the anatomic locations investigated. However, GDNF rescued the neurons of the facial motor nucleus, the mesencephalic nucleus and the median motor column in the absence of skeletal muscle. The findings of the current study agree with previous reports that compromised mouse neurons have increased survival response to GDNF.
胶质细胞源性神经营养因子(GDNF)在体外和体内均被认为是一种有效的神经元存活因子。本研究调查了在野生型以及Myf5-/-:MyoD-/-胚胎中进行单次子宫内注射GDNF的效果。后一组胚胎,即双突变体(DM),由于缺乏肌生成,不含有骨骼肌和相关神经营养因子,因此,中枢和外周神经系统的神经元会发生过度的程序性细胞死亡(EPCD)。我们发现,在所研究的任何解剖位置,GDNF处理对野生型神经元数量均无影响。然而,在没有骨骼肌的情况下,GDNF挽救了面神经运动核、中脑核和正中运动柱的神经元。本研究结果与先前的报道一致,即受损的小鼠神经元对GDNF的存活反应增强。