Sturrock R R
Neuropathol Appl Neurobiol. 1979 Nov-Dec;5(6):433-56. doi: 10.1111/j.1365-2990.1979.tb00642.x.
A quantitative study of changes in total cell number was carried out in the indusium griseum and anterior commissure from fetal life to old age in the mouse brain. The changes in the number of mitotic and pyknotic cells were recorded in the indusium griseum, anterior commissure, subependymal and ependymal layers over the same period. The number of neurons which are produced and which migrate to the indusium griseum are in excess of the number eventually required and the surplus neurons are lost by cell death in late gestation and early postnatal life while synaptogenesis and neuronal differentiation is taking place. This neuronal loss is associated with a rapid turnover of glia. Most first generation glia, or their immediate precursors, are produced prenatally, in parallel but one day behind neurons. There is no large burst of mitotic activity in the postnatal brain which gives rise to the myelination gliosis which is probably largely a migratory phenomenon. Cell division continues throughout life in all parts of the brain studied. The greatest mitotic activity is centred in the subependymal layer where mitotic cells substantially outnumber pyknotic ones. There is a gradual decrease in mitotic activity in the subependymal layer up to 9 months of age with fairly constant mitotic activity thereafter. Mitotic activity in the indusium griseum levels out at 3 months postnatum with mitotic and pyknotic cells present in roughly equal numbers thereafter. Mitotic activity in all parts of the anterior commissure levels out at 6 months postnatum and remains constant thereafter. Mitotic and pyknotic cells are present in similar numbers except for a peak in pyknotic cells at 9 months. Cell number in the indusium griseum and anterior commissure is fairly constant between 3 and 9 months, but glial number begins to decrease in all parts of the anterior commissure from 12 to 22 months. In the indusium griseum the number of glia increased slightly between 6 and 22 months. The number of neurons fluctuated during the first week after birth then remained constant until 18 months. There was a significant decrease in the number of neurons between 18 and 22 months.
对小鼠大脑从胎儿期到老年期的胼胝体和前连合中细胞总数的变化进行了定量研究。同期记录了胼胝体、前连合、室管膜下层和室管膜层中有丝分裂细胞和固缩细胞数量的变化。产生并迁移至胼胝体的神经元数量超过最终所需数量,多余的神经元在妊娠后期和出生后早期因细胞死亡而丢失,此时正在发生突触形成和神经元分化。这种神经元丢失与神经胶质细胞的快速更替有关。大多数第一代神经胶质细胞或其直接前体细胞在出生前产生,与神经元平行但比神经元晚一天。出生后大脑中没有大量的有丝分裂活动引发髓鞘形成性胶质增生,这可能主要是一种迁移现象。在所研究的大脑所有部位,细胞分裂终生持续。最大的有丝分裂活动集中在室管膜下层,其中有丝分裂细胞数量显著超过固缩细胞。室管膜下层的有丝分裂活动在9个月龄前逐渐减少,此后有丝分裂活动相当稳定。胼胝体中的有丝分裂活动在出生后3个月趋于平稳,此后有丝分裂细胞和固缩细胞数量大致相等。前连合所有部位的有丝分裂活动在出生后6个月趋于平稳,此后保持恒定。除了在9个月时固缩细胞出现峰值外,有丝分裂细胞和固缩细胞数量相似。胼胝体和前连合中的细胞数量在3至9个月之间相当稳定,但前连合所有部位的神经胶质细胞数量从12至22个月开始减少。在胼胝体中,神经胶质细胞数量在6至22个月之间略有增加。神经元数量在出生后第一周波动,然后保持恒定直至18个月。在18至22个月之间,神经元数量显著减少。