Grossman R, Fox L E, Gorovits R, Ben-Dror I, Reisfeld S, Vardimon L
Department of Biochemistry, George S. Wise Faculty of Life Sciences, Tel Aviv University, Israel.
Brain Res Mol Brain Res. 1994 Feb;21(3-4):312-20. doi: 10.1016/0169-328x(94)90262-3.
Glutamine synthetase (GS) is a differentiation marker of retina glial cell. It is expressed in the chicken neural retina at a particularly high level, is inducible by glucocorticoids and is always confined to Müller glia. This study investigated the molecular basis for tissue and cell-type specific expression of the GS gene. A high level of GS expression in the retina was found to coincide with the accumulation of a relatively high level of GS mRNA in this tissue. The gliatoxic agent alpha-aminoadipic acid, which can selectively destroy glia cells, was used to demonstrate that restriction of GS induction to Müller glia is controlled at a transcriptional level. Cortisol could induce accumulation of GS mRNA and transcription of the GS gene in Müller glia but not in retina neurons. Glia and neurons were also found to differ in their ability to express the glucocorticoid inducible CAT construct, p delta G46TCO, which is controlled by a 'simple GRE' promoter. When introduced into cells of retina tissue, this construct was cortisol-inducible in glia whereas in neurons it was only slightly inducible or not at all. Introduction of a glucocorticoid receptor expression vector into the cells facilitated induction of the CAT construct in neurons. Analysis by immunoblotting revealed that expression of the glucocorticoid receptor protein is predominantly restricted to Müller glia. These results suggest that differential levels of glucocorticoid receptor expression in glia and neurons might be the basis for cell-type specific induction of GS.
谷氨酰胺合成酶(GS)是视网膜神经胶质细胞的分化标志物。它在鸡的神经视网膜中表达水平特别高,可被糖皮质激素诱导,并且始终局限于米勒胶质细胞。本研究调查了GS基因组织和细胞类型特异性表达的分子基础。发现视网膜中高水平的GS表达与该组织中相对高水平的GS mRNA积累相一致。使用能选择性破坏胶质细胞的神经胶质毒性剂α-氨基己二酸来证明,GS诱导仅限于米勒胶质细胞是在转录水平上受到控制的。皮质醇可诱导米勒胶质细胞中GS mRNA的积累和GS基因的转录,但不能诱导视网膜神经元中的积累。还发现胶质细胞和神经元在表达由“简单糖皮质激素反应元件(GRE)”启动子控制的糖皮质激素诱导型氯霉素乙酰转移酶(CAT)构建体p delta G46TCO的能力上存在差异。当将该构建体引入视网膜组织细胞时,它在胶质细胞中可被皮质醇诱导,而在神经元中仅轻微诱导或根本不诱导。将糖皮质激素受体表达载体引入细胞可促进神经元中CAT构建体的诱导。免疫印迹分析表明,糖皮质激素受体蛋白的表达主要局限于米勒胶质细胞。这些结果表明,胶质细胞和神经元中糖皮质激素受体表达水平的差异可能是GS细胞类型特异性诱导的基础。