TY - JOUR
T1 - Multi-input synapses, but not LTP-strengthened synapses, correlate with hippocampal memory storage in aged mice
AU - Aziz, Wajeeha
AU - Kraev, Igor
AU - Mizuno, Keiko
AU - Kirby, Alastair James
AU - Fang, Ton
AU - Rupawala, Huzefa Jujar
AU - Kasbi, Kamillia
AU - Rothe, Stephanie
AU - Jozsa, Felix
AU - Rosenblum, Kobi
AU - Stewart, Michael
AU - Giese, Karl Peter
PY - 2019/11/4
Y1 - 2019/11/4
N2 - Long-lasting changes at synapses enable memory storage in the brain. Although aging is associated with impaired memory formation, it is not known whether the synaptic underpinnings of memory storage differ with age. Using a training schedule that results in the same behavioral memory formation in young and aged mice, we examined synapse ultrastructure and molecular signaling in the hippocampus after contextual fear conditioning. Only in young, but not old mice, contextual fear memory formation was associated with synaptic changes that characterize well-known, long-term potentiation, a strengthening of existing synapses with one input. Instead, old-age memory was correlated with generation of multi-innervated dendritic spines (MISs), which are predominantly two-input synapses formed by the attraction of an additional excitatory, presynaptic terminal onto an existing synapse. Accordingly, a blocker used to inhibit MIS generation impaired contextual fear memory only in old mice. Our results reveal how the synaptic basis of hippocampal memory storage changes with age and suggest that these distinct memory-storing mechanisms may explain impaired updating in old age.
AB - Long-lasting changes at synapses enable memory storage in the brain. Although aging is associated with impaired memory formation, it is not known whether the synaptic underpinnings of memory storage differ with age. Using a training schedule that results in the same behavioral memory formation in young and aged mice, we examined synapse ultrastructure and molecular signaling in the hippocampus after contextual fear conditioning. Only in young, but not old mice, contextual fear memory formation was associated with synaptic changes that characterize well-known, long-term potentiation, a strengthening of existing synapses with one input. Instead, old-age memory was correlated with generation of multi-innervated dendritic spines (MISs), which are predominantly two-input synapses formed by the attraction of an additional excitatory, presynaptic terminal onto an existing synapse. Accordingly, a blocker used to inhibit MIS generation impaired contextual fear memory only in old mice. Our results reveal how the synaptic basis of hippocampal memory storage changes with age and suggest that these distinct memory-storing mechanisms may explain impaired updating in old age.
U2 - 10.1016/j.cub.2019.08.064
DO - 10.1016/j.cub.2019.08.064
M3 - Article
SN - 0960-9822
VL - 29
SP - 3600-3610.e4
JO - Current biology : CB
JF - Current biology : CB
IS - 21
ER -