CCR5 is a suppressor for cortical plasticity and hippocampal learning and memory

Zhou, Miou, Greenhill, Stuart, Huang, Shan, Silva, Tawnie K., Sano, Yoshitake, Wu, Shumin, Cai, Ying, Nagaoka, Yoshiko, Sehgal, Megha, Cai, Denise J., Lee, Yong-Seok, Fox, Kevin and Silva, Alcino J. (2016). CCR5 is a suppressor for cortical plasticity and hippocampal learning and memory. eLife, 5 ,

Abstract

Although the role of CCR5 in immunity and in HIV infection has been studied widely, its role in neuronal plasticity, learning and memory is not understood. Here, we report that decreasing the function of CCR5 increases MAPK/CREB signaling, long-term potentiation (LTP), and hippocampus-dependent memory in mice, while neuronal CCR5 overexpression caused memory deficits. Decreasing CCR5 function in mouse barrel cortex also resulted in enhanced spike timing dependent plasticity and consequently, dramatically accelerated experience-dependent plasticity. These results suggest that CCR5 is a powerful suppressor for plasticity and memory, and CCR5 over-activation by viral proteins may contribute to HIV-associated cognitive deficits. Consistent with this hypothesis, the HIV V3 peptide caused LTP, signaling and memory deficits that were prevented by Ccr5 knockout or knockdown. Overall, our results demonstrate that CCR5 plays an important role in neuroplasticity, learning and memory, and indicate that CCR5 has a role in the cognitive deficits caused by HIV.

Publication DOI: https://doi.org/10.7554/eLife.20985
Divisions: Life & Health Sciences
Uncontrolled Keywords: neuroscience,plasticity,HIV,dementia,Neuroscience(all),Medicine(all),Immunology and Microbiology(all),Biochemistry, Genetics and Molecular Biology(all)
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Related URLs: http://www.scop ... tnerID=8YFLogxK (Scopus URL)
Published Date: 2016-12-20
Authors: Zhou, Miou
Greenhill, Stuart ( 0000-0002-5038-5258)
Huang, Shan
Silva, Tawnie K.
Sano, Yoshitake
Wu, Shumin
Cai, Ying
Nagaoka, Yoshiko
Sehgal, Megha
Cai, Denise J.
Lee, Yong-Seok
Fox, Kevin
Silva, Alcino J.

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License: Creative Commons Attribution


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