Vogel M W, Sunter K, Herrup K
Department of Human Genetics, Yale Medical School, New Haven, Connecticut 06510.
J Neurosci. 1989 Oct;9(10):3454-62. doi: 10.1523/JNEUROSCI.09-10-03454.1989.
Previous studies of wild-type mice or mutant-wild-type mouse chimeras using the neurological mutant staggerer have supported a numerical matching hypothesis for target-related cell death. However, analyses of chimeras of a second neurological mutant, lurcher, have suggested that there may be significant flexibility in the relationship between the numbers of pre- and postsynaptic neurons. Whereas in staggerer chimeras there is a strict proportionality between the number of cerebellar granule cells and their postsynaptic target, the Purkinje cells, in lurcher chimeras, Wetts and Herrup (1983) report a relative increase in granule cell survival. We have reexamined the numerical matching between Purkinje and granule cells in an additional 5 lurcher----wild-type and 4 wild-type----wild-type chimerase. Our findings confirm and extend the results of the previous study to show that there is a close correlation between the number of granule and Purkinje cells in +/Lc chimeras, but for any given number of Purkinje cells in the +/Lc chimeras, more granule cells survive than in staggerer chimeras or inbred mouse strains. Whereas the ratio of granule to Purkinje cells in staggerer chimeras or inbred mouse strains is constant across all target sizes, in +/Lc chimeras the ratio of granule cells to Purkinje cells increases as the number of target neurons decreases. It seems likely that the increased granule cell survival is somehow related to the delayed degeneration of the +/Lc fraction of target cells in the +/Lc chimeras. Among the possible explanations for the observed results, we favor the hypothesis that a trophic factor is produced in +/Lc chimeras in response to the deafferentation of Purkinje cells that is capable of rescuing granule cells from target-related cell death. Our preference is based, in part, on observations of the state of the dendritic tree of the wild-type Purkinje cells that survive in +/Lc chimeras (Caddy et al., 1986).
以往对野生型小鼠或使用神经学突变体蹒跚者的突变体 - 野生型小鼠嵌合体的研究支持了与靶标相关的细胞死亡的数字匹配假说。然而,对另一种神经学突变体“蹒跚者”的嵌合体分析表明,突触前和突触后神经元数量之间的关系可能存在显著的灵活性。在蹒跚者嵌合体中,小脑颗粒细胞数量与其突触后靶标浦肯野细胞之间存在严格的比例关系,而在“蹒跚者”嵌合体中,韦茨和赫鲁普(1983年)报告颗粒细胞存活率相对增加。我们重新检查了另外5个“蹒跚者” - 野生型和4个野生型 - 野生型嵌合体中浦肯野细胞和颗粒细胞之间的数字匹配情况。我们的研究结果证实并扩展了先前研究的结果,表明在 +/Lc嵌合体中颗粒细胞和浦肯野细胞数量之间存在密切相关性,但对于 +/Lc嵌合体中任何给定数量的浦肯野细胞,存活的颗粒细胞比在蹒跚者嵌合体或近交小鼠品系中更多。在蹒跚者嵌合体或近交小鼠品系中,颗粒细胞与浦肯野细胞的比例在所有靶标大小中都是恒定的,而在 +/Lc嵌合体中,颗粒细胞与浦肯野细胞的比例随着靶标神经元数量的减少而增加。颗粒细胞存活率的增加似乎在某种程度上与 +/Lc嵌合体中靶细胞 +/Lc部分的延迟退化有关。在对观察结果的可能解释中,我们倾向于这样的假说,即 +/Lc嵌合体中由于浦肯野细胞传入神经阻滞而产生一种营养因子,该因子能够使颗粒细胞免于与靶标相关的细胞死亡。我们的偏好部分基于对在 +/Lc嵌合体中存活的野生型浦肯野细胞树突状树状态的观察(卡迪等人,1986年)。