Moretto G, Walker D G, Lanteri P, Taioli F, Zaffagnini S, Xu R Y, Rizzuto N
Sezione di Neurologia, Dipartimento di Scienze Neurologiche e della Visione, Policlinico Borgo Roma, Università di Verona, I-37134 Verona, Italy.
Cell Tissue Res. 1996 Nov;286(2):257-62. doi: 10.1007/s004410050695.
The expression and modulation of mRNA for glial-cell-line-derived neurotrophic factor (GDNF) in human glial cells was investigated. Astrocyte cell cultures were isolated from human fetal brains, characterized by immunocytochemistry and maintained in vitro in conditions of high purity; sister cultures were exposed to protein kinase C (PKC) inhibitors for 20 min. Total RNA was extracted from the cell pellets, reverse-transcribed into cDNA and amplified by the polymerase chain reaction (PCR) with primers specific for GDNF. A reverse-transcription/PCR procedure was also performed on mRNA extracted from human fibroblast and lymphocyte cell lines. Human astrocytes grown in the absence of neurons expressed detectable amounts of mRNA for GDNF but no amplification products were observed in fibroblasts and lymphocytes, thus confirming that GDNF production was cell-type specific. After exposure to PKC inhibitors, a dramatic down-regulation of GDNF mRNA was observed in astrocyte cell cultures. Thus, human astrocytes are constitutively capable of producing GDNF, such trophic activity is restricted to neural cells, and PKC plays key roles in signal pathways that regulate the gene activation and production of GDNF.
研究了人神经胶质细胞中胶质细胞源性神经营养因子(GDNF)mRNA的表达及调控。从人胎脑中分离出星形胶质细胞培养物,通过免疫细胞化学进行鉴定,并在体外保持高纯度培养;将姐妹培养物用蛋白激酶C(PKC)抑制剂处理20分钟。从细胞沉淀中提取总RNA,逆转录成cDNA,并使用针对GDNF的特异性引物通过聚合酶链反应(PCR)进行扩增。还对从人成纤维细胞和淋巴细胞系中提取的mRNA进行了逆转录/PCR操作。在无神经元条件下生长的人星形胶质细胞表达可检测量的GDNF mRNA,但在成纤维细胞和淋巴细胞中未观察到扩增产物,从而证实GDNF的产生具有细胞类型特异性。在用PKC抑制剂处理后,在星形胶质细胞培养物中观察到GDNF mRNA显著下调。因此,人星形胶质细胞能够组成性地产生GDNF,这种营养活性仅限于神经细胞,并且PKC在调节GDNF基因激活和产生的信号通路中起关键作用。