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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Excess extracellular and low intracellular glutamate in poorly differentiating wobbler astrocytes and astrocyte recovery in glutamine-depleted culture medium.
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Excess extracellular and low intracellular glutamate in poorly differentiating wobbler astrocytes and astrocyte recovery in glutamine-depleted culture medium.

机译:分化差的摆动星形胶质细胞中过量的细胞外和低谷氨酸含量和谷氨酰胺缺乏培养基中星形胶质细胞的回收。

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The wobbler mouse develops an inherited motoneuronal degeneration of unknown origin in the spinal cord. Primary cultures of adult wobbler spinal cord astrocytes display abnormal morphological characteristics with fewer processes and paucity of cell-cell contacts. We have searched for a possible involvement of glutamate and glutamine intra- and extracellular accumulations in vitro in the abnormal differentiation of mutant astrocytes. We have found significantly higher glutamate and glutamine concentrations in the culture media of mutant astrocytes over a 3-day period compared with normal control astrocytes. Moreover, intracellular glutamate concentrations decreased substantially in mutant astrocytes, but intracellular glutamine concentrations remained unchanged. Furthermore, decreasing initial glutamine concentrations in the culture medium (glutamine-depleted medium) led to the recovery of normal extra- and intracellular concentrations of glutamate and recovery of quasi-normal morphological differentiation and increased cell-cell contacts, leading to an essentially normal looking astrocyte network after 3 days of culture. Under these conditions, which lead to recovery, the only remaining abnormality was the higher glutamine extracellular concentration attained in the originally depleted glutamine media. These findings suggest that mechanisms regulating glutamate/glutamine synthesis and/or influx/efflux are defective in wobbler astrocytes, leading to metabolic imbalance and possible cytotoxic effects characterized by disturbed intercellular networks and poor differentiation.
机译:摇摆小鼠在脊髓中发展出未知来源的遗传性神经元变性。成年摇晃的脊髓星形胶质细胞的原代培养显示出异常的形态学特征,具有较少的过程和很少的细胞间接触。我们搜索了谷氨酸和谷氨酰胺的细胞外和细胞外积累体外可能参与突变星形胶质细胞的异常分化。我们发现,与正常对照星形胶质细胞相比,在3天的时间内,突变型星形胶质细胞的培养基中谷氨酸和谷氨酰胺的浓度明显更高。而且,突变星形细胞中细胞内谷氨酸的浓度显着降低,但是细胞内谷氨酰胺的浓度保持不变。此外,降低培养基(缺乏谷氨酰胺的培养基)中的初始谷氨酰胺浓度会导致正常的细胞外和细胞内谷氨酸浓度的恢复以及准正常形态分化的恢复和细胞间接触的增加,从而导致外观基本正常培养3天后的星形胶质细胞网络。在导致恢复的这些条件下,唯一剩余的异常是在最初耗尽的谷氨酰胺培养基中获得的更高的谷氨酰胺细胞外浓度。这些发现表明,在摇晃的星形胶质细胞中,调节谷氨酸/谷氨酰胺合成和/或流入/流出的机制是有缺陷的,从而导致代谢失衡和可能的细胞毒性作用,其特征在于细胞间网络干扰和分化差。

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