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在分化不良的震颤小鼠星形胶质细胞中细胞外谷氨酸过量和细胞内谷氨酸含量低,以及在谷氨酰胺缺乏的培养基中星形胶质细胞的恢复。

Excess extracellular and low intracellular glutamate in poorly differentiating wobbler astrocytes and astrocyte recovery in glutamine-depleted culture medium.

作者信息

Hantaz-Ambroise D, Cambier D, Aït-Ikhlef A, Parvy P, Murawsky M, Rieger F

机构信息

INSERM U153, Hôpital Necker, Paris, France.

出版信息

J Neurochem. 1995 Sep;65(3):1199-204. doi: 10.1046/j.1471-4159.1995.65031199.x.

Abstract

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.

摘要

摇晃小鼠会发生脊髓中起源不明的遗传性运动神经元变性。成年摇晃小鼠脊髓星形胶质细胞的原代培养物呈现出异常的形态特征,其突起较少且细胞间接触稀少。我们探究了谷氨酸和谷氨酰胺在细胞内和细胞外的蓄积是否可能在体外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,突变星形胶质细胞在3天培养期内的培养基中谷氨酸和谷氨酰胺浓度显著更高。此外,突变星形胶质细胞内的谷氨酸浓度大幅下降,但细胞内谷氨酰胺浓度保持不变。此外,降低培养基中的初始谷氨酰胺浓度(谷氨酰胺缺乏培养基)可使谷氨酸的细胞外和细胞内浓度恢复正常,并使形态分化恢复到接近正常水平,增加细胞间接触,在培养3天后形成基本正常的星形胶质细胞网络。在这些导致恢复的条件下,唯一残留的异常是最初缺乏谷氨酰胺的培养基中达到的较高细胞外谷氨酰胺浓度。这些发现表明,调节谷氨酸/谷氨酰胺合成和/或流入/流出的机制在摇晃小鼠星形胶质细胞中存在缺陷,导致代谢失衡,并可能产生以细胞间网络紊乱和分化不良为特征的细胞毒性作用。

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