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Xu, X. J.

Publications and source records attributed to Xu, X. J..

3 recordsLinked to original sources

Unethical amnesia brain: Memory and metacognitive distortion induced by dishonesty

Unethical actions and decisions may distort human memory in two aspects: memory accuracy and metacognition. However, the neural and computational mechanisms underlying the metacognition distortion caused by repeated dishonesty remain largely unknown. Here, we performed two fMRI studies, including one replication study, with an information-sending task in the scanner. The main moral decision task in the scanner involves consistency and reward as two main factors, combined with a pre-scan and post-scan memory test together with mouse tracking. With multiple dimensions of metrics to measure metacognition, we test whether the inter-subject metacognition change correlates with how participants trade off consistency and reward. We find that the compression of representational geometry of reward in the orbitofrontal cortex (OFC) is correlated with both immediate and delayed metacognition changes. Also, the functional connectivity between the dorsolateral prefrontal cortex (DLPFC) and the left temporoparietal junction (lTPJ) under dishonest responses can predict both immediate and delayed metacognition changes in memory. These results suggest that decision-making, emotion, and memory-related brain regions together play a key role in metacognition change after immoral action, shedding light on the neural mechanism of the complex interplay between moral decisions, cognitive processes, and memory distortion. I did that, says my memory. I could not have done that, says my pride, and remains inexorable. Eventually - the memory yields. --Nietzsche[1]

neuroscience↗

Competition and Synergy of Arp2/3 and Formins in Nucleating Actin Waves

The assembly and disassembly of actin filaments and their regulatory proteins are crucial for maintaining cell structure or changing physiological state. However, because of the tremendous global impact of actin on diverse cellular processes, dissecting the specific role of actin regulatory proteins remains challenging. In this study, we employ actin waves that propagate on the cortex of mast cell to investigate the interplay between formins and the Arp2/3 complex in the nucleating and turnover of cortical actin. Our findings reveal that the recruitment of FMNL1 and mDia3 precedes the Arp2/3 complex in cortical actin waves. Membrane and GTPase-interaction can drive oscillations of FMNL1 in an actin-dependent manner, but active Cdc42 waves or constitutively-active FMNL1 mutant can form without actin waves. In addition to the apparent coordinated assembly of formins and Arp2/3, we further reveal their antagonism, where inhibition of Arp2/3 complex by CK-666 led to a transient increase in the recruitment of formins and actin polymerization. Our analysis suggest that the antagonism could not be explained for the competition between FMNL1 and Arp2/3 for monomeric actin. Rather, it is regulated by a limited pool of their common upstream regulator, Cdc42, whose level is negatively regulated by Arp2/3. Collectively, our study highlights the multifaceted interactions, cooperative or competitive, between formins and Arp2/3 complex, in the intricate and dynamic control of actin cytoskeletal network.

cell biology↗

Unveiling consistency in flexibility: the role of reward and cognitive control in moral decisions

Moral decisions are multifaceted with two essential aspects, flexibility and consistency. However, the interaction between these two and the underlying mechanisms is rarely studied. Here, we combined mouse-tracking and functional magnetic resonance imaging (fMRI) together in a value-based moral decision task, which allows us to quantify accumulative history responses as self-consistency. Using a multi-attribute time-dependent drift-diffusion model (tDDM), we disentangled the role of consistency and self-interest, highlighting the dominant role of cognitive-control-related regions. The drift rate of self-consistency was directly associated with the brain activity responsible for cognitive control, while the relationship between the reward and the activity of the related brain regions was mediated by the mouse-tracking index area under the curve(AUC). Dorsolateral prefrontal cortex was revealed as a hub connecting prACC and ventral striatum, whose functional connectivity was correlated with consistency drift rate and reward drift rate respectively. Furthermore, decision flexibility was quantified by choice entropy, which links to mouse tracking indices and the activity of cognitive -control related regions. Together, our study uncovers the interplay between self-consistency and reward in behavior, and highlights the key role of cognitive control in modulating these two attributes, thereby deepening our understanding of consistency and flexibility in moral decisions.

neuroscience↗