Fletcher T L, De Camilli P, Banker G
Department of Psychiatry, Albany Medical College, New York 12208.
J Neurosci. 1994 Nov;14(11 Pt 1):6695-706. doi: 10.1523/JNEUROSCI.14-11-06695.1994.
Hippocampal neurons in culture develop extensive axonal and dendritic arbors and form numerous synapses. Presynaptic specializations occur at sites of contact between axons and somata or dendrites but they do not appear until day 3 in culture, even though numerous contacts between cells develop within the first 24 hr (Fletcher et al., 1991). To determine whether this delay in the appearance of presynaptic specializations could be related to maturational events in the presynaptic axon or in the postsynaptic target, "heterochronic" cocultures were prepared by adding newly dissociated neurons to cultures containing mature neurons. The competence of axons to form presynaptic vesicle clusters in response to contact with the somata or dendrites of mature or immature neurons was determined by immunofluorescent staining for synapsin I or synaptophysin. After only 1 d of coculture, there was a fivefold increase in the number of synapses along the somata and dendrites of the mature neurons, compared to mature neurons cultured alone. If newly dissociated neurons were labeled with a fluorescent dye before coculture, dye-labeled axons frequently were colocalized with presynaptic specializations on mature cells. In contrast, when the axons of mature neurons contacted immature neurons, synapses were first observed only after coculture for 3 d. These results suggest that the axons of hippocampal neurons have the capacity to form presynaptic specializations soon after they emerge, provided they encounter appropriate targets, but that the cell bodies and dendrites of hippocampal neurons are not capable of inducing the formation of presynaptic specializations until they reach a critical stage of maturation.
培养的海马神经元会发育出广泛的轴突和树突分支,并形成大量突触。突触前特化出现在轴突与胞体或树突的接触部位,但直到培养第3天才会出现,尽管细胞间的大量接触在最初24小时内就已形成(弗莱彻等人,1991年)。为了确定突触前特化出现的这种延迟是否与突触前轴突或突触后靶点的成熟事件有关,通过将新解离的神经元添加到含有成熟神经元的培养物中来制备“异时性”共培养物。通过对突触素I或突触囊泡蛋白进行免疫荧光染色,确定轴突在与成熟或未成熟神经元的胞体或树突接触时形成突触前囊泡簇的能力。共培养仅1天后,与单独培养的成熟神经元相比,成熟神经元胞体和树突上的突触数量增加了五倍。如果在共培养前用荧光染料标记新解离的神经元,染料标记的轴突经常与成熟细胞上的突触前特化共定位。相反,当成熟神经元的轴突与未成熟神经元接触时,只有在共培养3天后才首次观察到突触。这些结果表明,海马神经元的轴突一旦出现,只要遇到合适的靶点,就有能力很快形成突触前特化,但海马神经元的胞体和树突在达到关键的成熟阶段之前,没有能力诱导突触前特化的形成。