Mendis D B, Brown I R
Department of Zoology, University of Toronto, Ont., Canada.
Brain Res Mol Brain Res. 1994 Jul;24(1-4):11-9. doi: 10.1016/0169-328x(94)90112-0.
The pattern of expression of the SPARC gene was examined during postnatal development of the mouse brain using in situ hybridization. At postnatal day 3 (P3), a strong signal representing SPARC mRNA was apparent in boundary layers such as the pia mater and the lining of the ventricles. By P12, increased levels of SPARC mRNA were noted in the cerebellum, midbrain and brain stem with a lower signal in more frontal areas, a pattern which was retained in the adult. This pronounced caudal versus frontal difference in SPARC mRNA levels was confirmed by Northern blot analysis. At P3, SPARC mRNA was detected in developing blood vessels in the cerebral cortex, suggesting a role for SPARC in angiogenesis. During development of the cerebellum, expression of SPARC mRNA became highly restricted to the Purkinje cellular layer and in the adult was localized to Bergmann glial cells rather than Purkinje neurons.
利用原位杂交技术,研究了小鼠出生后脑发育过程中SPARC基因的表达模式。在出生后第3天(P3),在诸如软脑膜和脑室衬里等边界层中,代表SPARC mRNA的强信号很明显。到P12时,在小脑、中脑和脑干中观察到SPARC mRNA水平升高,而在更靠前的区域信号较低,这种模式在成年小鼠中持续存在。Northern印迹分析证实了SPARC mRNA水平在尾侧与额侧存在明显差异。在P3时,在大脑皮质发育中的血管中检测到SPARC mRNA,表明SPARC在血管生成中发挥作用。在小脑发育过程中,SPARC mRNA的表达高度局限于浦肯野细胞层,在成年小鼠中则定位于伯格曼胶质细胞而非浦肯野神经元。