Klein R S, Fricker L D
Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY 10461.
Brain Res. 1992 Jan 13;569(2):300-10. doi: 10.1016/0006-8993(92)90643-n.
Cultured astrocytes have been found to express neuropeptides, neuropeptide processing enzymes and their mRNAs. Although astrocytes were shown to display regional variation in their expression of these mRNAs, it was unclear whether all astrocytes cultured from the same brain region express similar mRNA levels or if this expression is heterogeneous. We examined the individual heterogeneity of astrocytes cultured from several brain regions by in situ hybridization. Astrocytes derived from the frontal cortex, hypothalamus and cerebellum of neonatal rat brains were cultured for 3 weeks and then analyzed by in situ hybridization using 35S-labeled cRNA probes to carboxypeptidase E (CPE), proenkephalin (PE), and cyclophilin (1B15) mRNAs and an oligomeric probe complimentary to the first 45 bases of rat 18S rRNA. Frequency histograms generated by counting the grains produced over emulsion-coated cells demonstrated populations of astrocytes expressing high levels of mRNA for CPE and PE and a population expressing low to background levels of these mRNAs. In contrast, all cultured astrocytes expressed high levels of 1B15 mRNA and 18S rRNA. The percentage of cultured astrocytes expressing high levels of CPE mRNA was 42% for frontal cortex astrocytes and 23% for cerebellar astrocytes. While the percentages of cultured astrocytes expressing high levels of PE mRNA varied slightly between brain region (24-28%), the level of PE mRNA expression per cell showed greater variation between regions. The effect of culture density on the expression of PE mRNA was also examined. Approximately 55% of the cells in low density cultures expressed PE mRNA, while only 5-10% of the cells in high density cultures expressed this mRNA. These results indicate that cultured astrocytes display individual heterogeneity with regard to neuropeptide biosynthesis and that the expression of neuropeptides by these cells is regulated.
已发现培养的星形胶质细胞可表达神经肽、神经肽加工酶及其信使核糖核酸(mRNA)。尽管星形胶质细胞在这些mRNA的表达上显示出区域差异,但尚不清楚从同一脑区培养的所有星形胶质细胞是否表达相似的mRNA水平,或者这种表达是否具有异质性。我们通过原位杂交研究了从几个脑区培养的星形胶质细胞的个体异质性。从新生大鼠脑的额叶皮质、下丘脑和小脑分离出的星形胶质细胞培养3周,然后使用35S标记的羧肽酶E(CPE)、前脑啡肽(PE)和亲环蛋白(1B15)mRNA的cRNA探针以及与大鼠18S rRNA前45个碱基互补的寡聚探针进行原位杂交分析。通过对涂有乳胶的细胞上产生的银粒进行计数生成的频率直方图显示,存在表达高水平CPE和PE mRNA的星形胶质细胞群体以及表达低至背景水平这些mRNA的群体。相比之下,所有培养的星形胶质细胞均表达高水平的1B15 mRNA和18S rRNA。额叶皮质星形胶质细胞中表达高水平CPE mRNA的培养星形胶质细胞百分比为42%,小脑星形胶质细胞为23%。虽然不同脑区中表达高水平PE mRNA的培养星形胶质细胞百分比略有差异(24 - 28%),但每个细胞的PE mRNA表达水平在不同区域间差异更大。还研究了培养密度对PE mRNA表达的影响。低密度培养物中约55%的细胞表达PE mRNA,而高密度培养物中只有5 - 10%的细胞表达该mRNA。这些结果表明,培养的星形胶质细胞在神经肽生物合成方面表现出个体异质性,并且这些细胞中神经肽的表达受到调控。