Hu R M, Levin E R
Department of Medicine, University of California at Irvine 92717.
J Clin Invest. 1994 Apr;93(4):1820-7. doi: 10.1172/JCI117167.
The important intracellular mechanisms of astrocyte growth are not well defined. Using an inhibitor of astrocyte proliferation, atrial natriuretic peptide (ANP), and the glial mitogen endothelin (ET-3), we sought a common pathway for growth regulation in these neural cells. In cultured fetal rat diencephalic astrocytes, ANP selectively and rapidly inhibited the Tis 8 immediate early gene and protein. After 4 h, ANP selectively inhibited the basic fibroblast growth factor (bFGF) gene and protein. ET-3 significantly stimulated both Tis 8 and bFGF mRNAs and protein, but also stimulated several other immediate early and growth factor/receptor genes. An antisense oligonucleotide to Tis 8 strongly prevented ET-stimulated thymidine incorporation, while the inhibitory action of ANP was enhanced. The Tis 8 antisense oligonucleotide also significantly reversed ET-stimulated bFGF transcription and enhanced the bFGF inhibition caused by ANP. In addition, an antisense oligonucleotide to bFGF significantly reversed the ET-stimulated thymidine incorporation and enhanced the ANP inhibition of DNA synthesis. The sequential modulation of Tis 8, followed by bFGF, provides a novel mechanism for both positive and negative regulation of astrocyte growth by endogenous neuropeptides.
星形胶质细胞生长的重要细胞内机制尚未明确界定。利用星形胶质细胞增殖抑制剂心房利钠肽(ANP)和神经胶质有丝分裂原内皮素(ET-3),我们探寻了这些神经细胞生长调节的共同途径。在培养的胎鼠间脑星形胶质细胞中,ANP选择性且快速地抑制了Tis 8即刻早期基因和蛋白。4小时后,ANP选择性地抑制了碱性成纤维细胞生长因子(bFGF)基因和蛋白。ET-3显著刺激了Tis 8和bFGF的mRNA及蛋白,同时也刺激了其他几个即刻早期基因以及生长因子/受体基因。针对Tis 8的反义寡核苷酸强烈阻止了ET刺激的胸苷掺入,而ANP的抑制作用增强。Tis 8反义寡核苷酸还显著逆转了ET刺激的bFGF转录,并增强了ANP对bFGF的抑制作用。此外,针对bFGF的反义寡核苷酸显著逆转了ET刺激的胸苷掺入,并增强了ANP对DNA合成的抑制作用。先对Tis 8进行调节,随后调节bFGF,这为内源性神经肽对星形胶质细胞生长的正负调节提供了一种新机制。