Impaired long-term potentiation and long-term memory deficits in xCT-deficient sut mice

Author:

Li Yan12,Tan Zhibing3,Li Zhigang4,Sun Zhongsheng4,Duan Shumin3,Li Wei1

Affiliation:

1. State Key Laboratory of Molecular Developmental Biology, Institute of Genetics & Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China

2. Graduate School of Chinese Academy of Sciences, 19 Yuquan Road, Beijing 100039, China

3. Department of Neurobiology, Zhejiang University School of Medicine, Hangzhou 310058, China

4. Beijing Institutes of Life Science, Chinese Academy of Sciences, Beijing 100101, China

Abstract

xCT is the functional subunit of the cystine/glutamate antiporter system xc−, which exchanges intracellular glutamate with extracellular cystine. xCT has been reported to play roles in the maintenance of intracellular redox and ambient extracellular glutamate, which may affect neuronal function. To assess a potential role of xCT in the mouse hippocampus, we performed fear conditioning and passive avoidance for long-term memories and examined hippocampal synaptic plasticity in wild-type mice and xCT-null mutants, sut mice. Long-term memory was impaired in sut mice. Normal basal synaptic transmission and short-term presynaptic plasticity at hippocampal Schaffer collateral–CA1 synapses were observed in sut mice. However, LTP (long-term potentiation) was significantly reduced in sut mice compared with their wild-type counterparts. Supplementation of extracellular glutamate did not reverse the reduction in LTP. Taken together, our results suggest that xCT plays a role in the modulation of hippocampal long-term plasticity.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

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