Ichikawa M, Muramoto K, Kobayashi K, Kawahara M, Kuroda Y
Department of Anatomy and Embryology, Tokyo Metropolitan Institute for Neuroscience, Japan.
Neurosci Res. 1993 Feb;16(2):95-103. doi: 10.1016/0168-0102(93)90076-3.
Cerebral cortical cells from fetal rats (18 days) were cultured for 3, 7, 14, 21, 28, 35 days in vitro (DIV) and the development of synapses was examined morphologically by electron microscopy. At 3 DIV, no synapses could be recognized. An immature type of synapse was found at 7 DIV which thereafter developed morphologically. The length of the synaptic contact zone (SCZ) increased with DIV from 271 +/- 11.4 nm (mean +/- SEM) at 7 DIV to 410 +/- 11.4 nm at 35 DIV. The number of synaptic vesicles per terminal also increased with DIV: 10.0 +/- 1.2 at 7 DIV, 35.7 +/- 3.4 at 21 DIV, and 53.3 +/- 4.5 at 35 DIV. The time course of numerical density of synapses was examined quantitatively by electron microscopy. Synaptic density was very low at 7 DIV. It was significantly increased at 14 DIV and thereafter showed variable changes. Four culture series showed decreases after 14 DIV, but one series showed a further increase at 21 DIV followed by a decrease at 28 DIV. The mean density of synapses at each DIV was as follows: 1780 +/- 86/10(6) microns3 at 7 DIV, 4244 +/- 595/10(6) microns3 at 14 DIV, 2285 +/- 674/10(6) microns3 at 21 DIV, 2552 +/- 646/10(6) microns3 at 28 DIV, and 2080 +/- 532/10(6) microns3 at 35 DIV. Neuronal cell density was counted in each culture to calculate the relative number of synapses per neuron. The cell density decreased with age from 301 +/- 51/10(6) microns3 at 7 DIV to 39 +/- 9/10(6) microns3 at 35 DIV.(ABSTRACT TRUNCATED AT 250 WORDS)
取自胎鼠(18日龄)的大脑皮质细胞在体外培养3、7、14、21、28、35天(体外培养天数,DIV),并通过电子显微镜从形态学上检查突触的发育情况。在体外培养3天时,未识别出突触。在体外培养7天时发现了一种不成熟类型的突触,此后其在形态上不断发育。突触接触区(SCZ)的长度随着体外培养天数增加,从体外培养7天时的271±11.4纳米(平均值±标准误)增加到体外培养35天时的410±11.4纳米。每个终末的突触小泡数量也随着体外培养天数增加:体外培养7天时为10.0±1.2个,体外培养21天时为35.7±3.4个,体外培养35天时为53.3±4.5个。通过电子显微镜对突触数量密度的时间进程进行了定量检查。突触密度在体外培养7天时非常低。在体外培养14天时显著增加,此后呈现出不同的变化。四个培养系列在体外培养14天后显示下降,但一个系列在体外培养21天时进一步增加,随后在体外培养28天时下降。每个体外培养天数时突触的平均密度如下:体外培养7天时为1780±86/10⁶立方微米,体外培养14天时为4244±595/10⁶立方微米,体外培养21天时为2285±674/10⁶立方微米,体外培养28天时为2552±646/10⁶立方微米,体外培养35天时为2080±532/10⁶立方微米。计算每个培养物中的神经元细胞密度,以计算每个神经元的相对突触数量。细胞密度随着年龄增长而降低,从体外培养7天时的301±5I/10⁶立方微米降至体外培养35天时的39±9/10⁶立方微米。(摘要截选至250字)