Jain Anant, Nakahata Yoshihisa, Watabe Tetsuya, Rusina Polina, South Kelly, Adachi Kengo, Yan Long, Simorowski Noriko, Furukawa Hiro, Yasuda Ryohei
bioRxiv. 2023 Aug 1:2023.08.01.549180. doi: 10.1101/2023.08.01.549180.
Behavioral time scale plasticity (BTSP), is a form of non-Hebbian plasticity induced by integrating pre- and postsynaptic components separated by behavioral time scale (seconds). BTSP in the hippocampal CA1 neurons underlies place cell formation. However, the molecular mechanisms underlying this behavioral time scale (eligibility trace) and synapse specificity are unknown. CaMKII can be activated in a synapse-specific manner and remain active for a few seconds, making it a compelling candidate for the eligibility trace during BTSP. Here, we show that BTSP can be induced in a single dendritic spine using 2-photon glutamate uncaging paired with postsynaptic current injection temporally separated by behavioral time scale. Using an improved CaMKII sensor, we saw no detectable CaMKII activation during this BTSP induction. Instead, we observed a dendritic, delayed, and stochastic CaMKII activation (DDSC) associated with Ca influx and plateau 20-40 s after BTSP induction. DDSC requires both pre-and postsynaptic activity, suggesting that CaMKII can integrate these two signals. Also, optogenetically blocking CaMKII 30 s after the BTSP protocol inhibited synaptic potentiation, indicating that DDSC is an essential mechanism of BTSP. IP3-dependent intracellular Ca release facilitates both DDSC and BTSP. Thus, our study suggests that the non-synapse specific CaMKII activation provides an instructive signal with an extensive time window over tens of seconds during BTSP.
行为时间尺度可塑性(BTSP)是一种非赫布可塑性形式,由整合行为时间尺度(秒)分隔的突触前和突触后成分所诱导。海马体CA1神经元中的BTSP是位置细胞形成的基础。然而,这种行为时间尺度(资格痕迹)和突触特异性背后的分子机制尚不清楚。钙/钙调蛋白依赖性蛋白激酶II(CaMKII)可以以突触特异性方式被激活,并在几秒钟内保持活跃,这使其成为BTSP期间资格痕迹的有力候选者。在这里,我们表明,使用双光子谷氨酸解笼结合行为时间尺度上暂时分开的突触后电流注入,可以在单个树突棘中诱导BTSP。使用一种改进的CaMKII传感器,我们在这种BTSP诱导过程中未检测到可检测到的CaMKII激活。相反,我们观察到与BTSP诱导后20 - 40秒的钙内流和平原相关的树突状、延迟和随机的CaMKII激活(DDSC)。DDSC需要突触前和突触后活动,这表明CaMKII可以整合这两个信号。此外,在BTSP方案后30秒用光遗传学方法阻断CaMKII可抑制突触增强,表明DDSC是BTSP的一种基本机制。三磷酸肌醇(IP3)依赖性细胞内钙释放促进DDSC和BTSP。因此,我们的研究表明,非突触特异性CaMKII激活在BTSP期间提供了一个在数十秒的广泛时间窗口内具有指导意义的信号。