Timescales of Local and Cross-Area Interactions during Neuroprosthetic Learning.

How does the brain integrate signals with different timescales to drive purposeful actions? Brain-machine interfaces (BMIs) offer a powerful tool to causally test how distributed neural networks achieve specific neural patterns. During neuroprosthetic learning, actuator movements are causally linked to primary motor cortex (M1) neurons, i.e., "direct" neurons that project to the decoder and whose firing is required to successfully perform the task. However, it is unknown how such direct M1 neurons interact with both "indirect" local (in M1 but not part of the decoder) and across area neural populations (e.g., in premotor cortex/M2), all of which are embedded in complex biological recurrent networks. Here, we trained male rats to perform a M1-BMI task and simultaneously recorded the activity of indirect neurons in both M2 and M1. We found that both M2 and M1 indirect neuron populations could be used to predict the activity of the direct neurons (i.e., "BMI-potent activity"). Interestingly, compared with M1 indirect activity, M2 neural activity was correlated with BMI-potent activity across a longer set of time lags, and the timescale of population activity patterns evolved more slowly. M2 units also predicted the activity of both M1 direct and indirect neural populations, suggesting that M2 population dynamics provide a continuous modulatory influence on M1 activity as a whole, rather than a moment-by-moment influence solely on neurons most relevant to a task. Together, our results indicate that longer timescale M2 activity provides modulatory influence over extended time lags on shorter-timescale control signals in M1. A central question in the study of motor control is whether primary motor cortex (M1) and premotor cortex (M2) interact through task-specific subpopulations of neurons, or whether tasks engage broader correlated networks. Brain-machine interfaces (BMIs) are powerful tools to study cross-area interactions. Here, we performed simultaneous recordings of M1 and M2 in a BMI task using a subpopulation of M1 neurons (direct neurons). We found that activity outside of direct neurons in M1 and M2 was predictive of M1-BMI task activity, and that M2 activity evolved at slower timescales than M1. These findings suggest that M2 provides a continuous modulatory influence on M1 as a whole, supporting a model of interactions through broad correlated networks rather than task-specific neural subpopulations.