Wedler F C, Vichnin M C, Ley B W, Tholey G, Ledig M, Copin J C
Dept. of Molecular & Cell Biology, Althouse Laboratory, Pennsylvania State University, University Park 16802.
Neurochem Res. 1994 Feb;19(2):145-51. doi: 10.1007/BF00966809.
Previous studies have demonstrated that in glia and astrocytes Mn(II) is distributed with ca. 30-40% in the cytoplasm, 60-70% in mitochondria. Ca(II) ions were observed to alter both the flux rates and distribution of Mn(II) ions in primary cultures of chick glia and rat astrocytes. External (influxing) Ca(II) ions had the greatest effect on Mn(II) uptake and efflux, compared to internal (effluxing) or internal-external equilibrated Ca(II) ions. External (influxing) Ca(II) ions inhibited the net rate and extent of Mn(II) uptake but enhanced Mn(II) efflux from mitochondria. These observations differ from Ca(II)-Mn(II) effects previously reported with "brain" (neuronal) mitochondria. Overall, increased cytoplasmic Ca(II) acts to block Mn(II) uptake and enhance Mn(II) release by mitochondria, which serve to increase the cytoplasmic concentration of free Mn(II). A hypothesis is presented involving external L-glutamate acting through membrane receptors to mobilize cell Ca(II), which in turn causes mitochondrial Mn(II) to be released. Because the concentration of free cytoplasmic Mn(II) is poised near the Kd for Mn(II) with glutamine synthetase, a slight increase in cytoplasmic Mn(II) will directly enhance the activity of glutamine synthetase, which catalyzes removal of neurotoxic glutamate and ammonia.
先前的研究表明,在神经胶质细胞和星形胶质细胞中,锰离子(Mn(II))的分布情况为:约30 - 40%在细胞质中,60 - 70%在线粒体中。在鸡神经胶质细胞和大鼠星形胶质细胞的原代培养物中,观察到钙离子(Ca(II))会改变锰离子(Mn(II))的通量速率和分布。与内部(流出)或内部 - 外部平衡的钙离子(Ca(II))相比,外部(流入)的钙离子(Ca(II))对锰离子(Mn(II))的摄取和流出影响最大。外部(流入)的钙离子(Ca(II))抑制了锰离子(Mn(II))摄取的净速率和程度,但增强了锰离子(Mn(II))从线粒体的流出。这些观察结果与先前报道的“脑”(神经元)线粒体中钙离子(Ca(II)) - 锰离子(Mn(II))的效应不同。总体而言,细胞质中钙离子(Ca(II))增加会阻止锰离子(Mn(II))的摄取,并增强线粒体对锰离子(Mn(II))的释放,这会增加细胞质中游离锰离子(Mn(II))的浓度。本文提出了一个假说,即外部L - 谷氨酸通过膜受体作用来动员细胞内的钙离子(Ca(II)),进而导致线粒体释放锰离子(Mn(II))。由于细胞质中游离锰离子(Mn(II))的浓度接近谷氨酰胺合成酶对锰离子(Mn(II))的解离常数(Kd),细胞质中锰离子(Mn(II))的轻微增加将直接增强谷氨酰胺合成酶的活性,该酶催化去除神经毒性谷氨酸和氨。