Wu G, Lu Z H, Ledeen R W
Department of Neurosciences, New Jersey Medical School, UMDNJ, Newark 07103, USA.
J Neurochem. 1995 Sep;65(3):1419-22. doi: 10.1046/j.1471-4159.1995.65031419.x.
GM1 in the nuclear membrane, previously shown to be up-regulated during neurite outgrowth, has been found to influence nuclear Ca2+ flux during differentiation of Neuro-2a cells. Nuclei were isolated from cultured Neuro-2a cells before and after neuraminidase-induced neuritogenesis and incubated with 45Ca2+ for varying periods to determine uptake/efflux of Ca2+. At 5, 10, and 15 min 45Ca2+ levels in nuclei from differentiated cells were significantly lower than those in nuclei from untreated cells. The same result was obtained when the GM1 level was elevated artificially by preincubation of the nuclei in 10 microM GM1. In experiments designed to measure efflux specifically, isolated nuclei preincubated in GM1 released 45Ca2+ more rapidly than untreated nuclei. We conclude that one role of GM1 in the nuclear membrane is to alter Ca2+ regulatory mechanisms in the nucleus following onset of neuronal process outgrowth.
核膜中的GM1,先前已证明在神经突生长过程中上调,现已发现其在Neuro-2a细胞分化过程中影响核Ca2+通量。在神经氨酸酶诱导神经突形成前后,从培养的Neuro-2a细胞中分离细胞核,并与45Ca2+孵育不同时间,以确定Ca2+的摄取/流出。在5、10和15分钟时,分化细胞细胞核中的45Ca2+水平显著低于未处理细胞细胞核中的水平。当通过在10 microM GM1中预孵育细胞核人为提高GM1水平时,也得到了相同的结果。在专门设计用于测量流出的实验中,在GM1中预孵育的分离细胞核比未处理的细胞核更快地释放45Ca2+。我们得出结论,核膜中GM1的一个作用是在神经元突起生长开始后改变细胞核中的Ca2+调节机制。