On Dec. 12, 2025, a Japanese research team announced it has successfully reproduced the human neural circuit in vitro using multi-region miniature organs known as assembloids, which are derived from induced pluripotent stem (iPS) cells. With this circuit, the team demonstrated that the thalamus plays a crucial role in shaping cell type-specific neural circuits in the human cerebral cortex.

Our brain’s cerebral cortex contains various types of neurons, and effective communication among these neurons and other brain regions is crucial for activating functions like perception and cognition. Patients with neurodevelopmental disorders, such as autism spectrum disorder (ASD), exhibit disruptions in the structure and function of neural circuits in the cerebral cortex. Therefore, understanding the principles of these circuits is essential to uncovering the causes of these disorders and developing new medications.

The researchers began by generating cortical and thalamic organoids from human iPS cells. They then physically fused these organoids to create assembloids and studied the thalamus-cortex interactions within them. Their observations revealed that axons in the thalamus extended toward the cortex, whereas those in the cortex extended toward the thalamus, forming synapses with one another. These findings demonstrated that thalamus-cortex interactions in the assembloid operate similarly to those in the human brain.

The researchers also examined how these thalamus-cortex interactions contribute to the formation of neural circuits in the cortex of the assembloid. They discovered that neural activity propagates from the thalamus to the cortex in a wave-like pattern, forming a synchronous network within the cortex.

Furthermore, the team measured neural activity levels in three primary subtypes of cortical excitatory neurons: intratelencephalic (IT), pyramidal tract (PT), and corticothalamic (CT). They aimed to identify which types of neurons contribute to synchronous neural activity networks.

The results revealed synchronous activity in PT and CT neurons, both of which project to the thalamus. In contrast, no synchrony was observed in IT neurons. These findings suggest that thalamic inputs selectively promote the formation of cell type-specific synchronized networks, enhancing their functional maturation in the assembloid.

The research team successfully reproduced human neural circuits using assembloids. This achievement provides a system to analyze the origins, structures, and functions of these circuits at the cell-type level. These findings were published in the journal Proceedings of the National Academy of Sciences.