Vogel M W, Sinclair M, Qiu D, Fan H
Maryland Psychiatric Research Center, University of Maryland Medical School, P.O. Box 21247, Baltimore, Maryland 21228, USA.
J Neurobiol. 2000 Feb 15;42(3):323-37. doi: 10.1002/(sici)1097-4695(20000215)42:3<323::aid-neu4>3.0.co;2-2.
Staggerer (sg/sg) is an autosomal recessive mutation in an orphan nuclear hormone receptor gene, RORalpha, that causes a cell-autonomous, lineage-specific block in the development of the Purkinje cell. Purkinje cell number is reduced by about 75-90% in adult mutants, and many of the surviving cells are small and ectopically positioned. To determine whether Purkinje cell numbers are reduced owing to either agenesis or cell death, cohorts of Purkinje cells were labeled with the birth-date marker bromodeoxyuridine (BrdU) at embryonic day (E) 10.5 or E11.5. The total number of BrdU-labeled profiles was then compared between cerebella from wild-type mice, heterozygous staggerer, and staggerer mutants at E17.5 and postnatal day (P)5. There was no significant difference between sg/sg mutants and +/sg or +/+ controls in the number of BrdU-labeled profiles or in cerebellar volumes in the E17 embryos. By P5, however, cerebellar volume was significantly reduced in the sg/sg mutants compared to controls (p <.005) and the number of BrdU-labeled profiles was reduced by 33% following E11.5 BrdU injections (p <.02). The results suggest that Purkinje cell genesis is not affected by the staggerer mutation and that Purkinje cell loss begins some time after E17. RORalpha is highly expressed in Purkinje cells by E14, so the delay between initial RORalpha expression and sg/sg Purkinje cell loss suggests that the staggerer mutation does not directly cause Purkinje cell death.
蹒跚症小鼠(sg/sg)是一种常染色体隐性突变体,其孤儿核激素受体基因RORα发生突变,导致浦肯野细胞发育出现细胞自主性、谱系特异性阻滞。成年突变体中浦肯野细胞数量减少约75 - 90%,许多存活细胞体积小且位置异常。为了确定浦肯野细胞数量减少是由于发育不全还是细胞死亡,在胚胎期第(E)10.5天或E11.5天,用出生日期标记物溴脱氧尿苷(BrdU)标记浦肯野细胞群。然后比较野生型小鼠、杂合蹒跚症小鼠和蹒跚症突变体在E17.5和出生后第(P)5天小脑之间BrdU标记轮廓的总数。在E17胚胎中,sg/sg突变体与 +/sg或 +/+ 对照在BrdU标记轮廓数量或小脑体积上没有显著差异。然而,到P5时,与对照组相比,sg/sg突变体的小脑体积显著减小(p <.005),并且在E11.5注射BrdU后,BrdU标记轮廓数量减少了33%(p <.02)。结果表明,浦肯野细胞的发生不受蹒跚症突变的影响,并且浦肯野细胞的损失在E17之后的某个时间开始。到E14时,RORα在浦肯野细胞中高度表达,因此初始RORα表达与sg/sg浦肯野细胞损失之间的延迟表明,蹒跚症突变不会直接导致浦肯野细胞死亡。