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Home Brain Research

Right-to-Left Brain Circuit Essential for Navigation

Editorial Team by Editorial Team
April 14, 2026
in Brain Research
Right-to-Left Brain Circuit Essential for Navigation
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Summary: For the first time, scientists have identified a specific neural “bridge” between the two halves of the hippocampus that is essential for spatial memory. The study describes a circuit where neurons in the right CA1 region project directly to the left subiculum.

This interhemispheric connection is the key to how we navigate and remember locations. Furthermore, researchers discovered that this circuit is significantly weakened in models of schizophrenia, offering a potential neural explanation for the cognitive and spatial disorientation often seen in neuropsychiatric disorders.

Key Facts

  • The New Pathway: The circuit links the right hippocampal CA1 region to the left hippocampal subiculum.
  • Spatial Necessity: Using optogenetics (controlling neurons with light), researchers proved that blocking this specific “bridge” makes mice unable to remember locations or navigate effectively, while leaving their anxiety levels and basic object recognition untouched.
  • The Schizophrenia Link: The study utilized a mouse model of the 22q11.2 deletion (a major genetic risk factor for schizophrenia). These mice showed a marked reduction in these interhemispheric connections and significant spatial memory deficits.
  • Gender Divergence: While the genetic alteration affected both sexes, males demonstrated more pronounced cognitive deficits in spatial testing.
  • Clinical Potential: Researchers believe this circuit could eventually be monitored in humans using tractography (advanced neuroimaging) to help detect or diagnose brain alterations associated with schizophrenia early on.

Source: UMH

A team led by the Institute for Neurosciences (IN), a joint center of the Spanish National Research Council (CSIC) and Miguel Hernández University of Elche (UMH), has identified a brain circuit essential for spatial memory.

The study, published in Cell Reports, describes for the first time a connection between the two hippocampal hemispheres, in which neurons in the CA1 region of the right hemisphere send projections to the left hemisphere, specifically to the subiculum.

The results show that this communication is necessary for navigation and remembering locations. Moreover, the study reveals that this circuit is altered in mice carrying a genetic mutation associated with schizophrenia.

“We knew that the hippocampus is key for memory, but we did not fully understand how its two hemispheres communicate. In this work, we identified a specific pathway and demonstrated that it is necessary for fundamental cognitive functions”, explains Félix Leroy, the principal investigator of the study and director of the Cognition and Social Interactions Laboratory at the Institute for Neurosciences.

A “Bridge” Between Hemispheres for Memory

The brain is divided into two hemispheres that process information in a partially specialized manner, yet they need to coordinate constantly. However, the specific connections that enable this communication in regions involved in memory, such as the hippocampus, are largely unknown.

In this work, the team identified one of these connections: a neuronal projection linking the CA1 region of the right hemisphere with the subiculum of the left hemisphere. To do this, the researchers used neuronal tracing techniques that allow them to follow the path of connections between neurons.

“This circuit acts as a bridge between the two regions and enables the integration of information needed to navigate and remember the locations of things”, says Noelia Sofía de León Reyes, the first author of the study.

To test the function of this circuit, the researchers used optogenetic tools, which allow the activity of specific neurons to be controlled with light. In this way, they were able to selectively block this connection in mice and observe its effects on behavior.

The results show that when this interhemispheric communication is disrupted, mice have difficulty remembering the location of objects and making decisions in tasks that require spatial memory. However, other functions, such as anxiety or object recognition, remain intact.

“This indicates that this connection is not merely structural, but has a very specific role in spatial memory”, adds Leroy.

The team also studied this connection in a mouse model carrying a genetic alteration equivalent to the 22q11.2 deletion, a human condition that significantly increases the risk of developing schizophrenia and other neuropsychiatric disorders.

In these animals, the researchers observed both spatial memory deficits and a reduction in interhemispheric hippocampal connections. Additionally, although the alteration is present in both sexes, males showed more pronounced deficits in some tests.

“We observed that when this circuit is altered, the ability to navigate and remember is also affected. This suggests that interhemispheric disconnection could contribute to cognitive problems in psychiatric disorders”, explains De León Reyes.

The results provide a new piece of the puzzle for understanding how the brain integrates information between hemispheres and how its disruption can lead to cognitive deficits.

Additionally, the authors note that this finding could have long-term clinical implications. “These types of connections could be studied in humans using neuroimaging techniques, such as tractography, combined with cognitive tests”, notes Leroy.

“In the long term, this could contribute to the development of new strategies for detecting brain alterations associated with disorders such as schizophrenia”.

The work combines different experimental approaches in mice to identify and analyze this brain circuit.

The study involved collaboration with the laboratory of Marta Nieto from the Spanish National Center for Biotechnology (CNB-CSIC). While doing her PhD in the Nieto’s lab, Noelia Sofía de León Reyes began working on hippocampal interhemispheric connections and collected preliminary results.

The study also involved Joseph A. Gogos from Columbia University (United States) who created the Df16(A) mouse model of 22q11 microdeletion, and incorporated the use of viral tools for manipulating neuronal circuit analysis with the participation of IN CSIC-UMH expert Cristina García Frigola.

Funding: This work was possible thanks to funding from the European Research Council (ERC) under the Horizon 2020 research and innovation program of the European Union, the Spanish State Research Agency – Ministry of Science, Innovation and Universities through the Severo Ochoa Program for Centers of Excellence, the Generalitat Valenciana, the “la Caixa” Foundation, the Severo Ochoa Foundation, and National Institute of Mental Health (NIMH) of the United States.

This research is part of the MotivatedBehaviors project (H2020-ERC-STG/0784, no. 949652), which aims to study the role of the lateral septum in regulating motivated behaviors to reveal changes that occur in disorders associated with deficits in social behavior.

Key Questions Answered:

Q: Why does the brain need a “bridge” between hemispheres just to remember where I parked?

A: The two halves of the brain often specialize in different types of information. Spatial navigation is complex; it requires integrating your current “map” with your past “memories.” This newly discovered bridge allows the right and left hippocampus to coordinate in real-time, turning raw data into a functional 3D mental map.

Q: What does this discovery have to do with schizophrenia?

A: Schizophrenia is often associated with “disconnection.” This study provides a physical example: a specific neural highway that is literally thinning out. When the two sides of the memory center can’t “talk” to each other efficiently, it leads to the confusion and spatial memory struggles often reported by patients.

Q: Can we “fix” this bridge in humans?

A: We aren’t there yet, but identifying the exact coordinates is the first step. Knowing that the right CA1 and left subiculum are the key players allows researchers to look for ways to strengthen these connections, perhaps through targeted neuro-stimulation or specific cognitive therapies.

Editorial Notes:

  • This article was edited by a Neuroscience News editor.
  • Journal paper reviewed in full.
  • Additional context added by our staff.

About this neuroscience research news

Author: Angeles Gallar
Source: UMH
Contact: Angeles Gallar – UMH
Image: The image is credited to Neuroscience News

Original Research: Open access.
“Interhemispheric CA1 projections to the subiculum support spatial cognition and are affected in a mouse model of the 22q11.2 deletion syndrome” by Noelia S. de León Reyes, Maria Helena Bortolozzo-Gleich, Helden Natalia Velez Gonzalez, Yuki Nomura, Cristina García Frigola, Marta Nieto, Joseph A. Gogos, and Félix Leroy. Cell Reports
DOI:10.1016/j.celrep.2026.117114


Abstract

Interhemispheric CA1 projections to the subiculum support spatial cognition and are affected in a mouse model of the 22q11.2 deletion syndrome

Mapping hippocampal connectivity is essential to understand the neural mechanisms of learning and memory, yet interhemispheric connections between hippocampal formations remain poorly defined.

In rodents, two main commissural pathways are known: dentate gyrus hilar mossy cells project to the inner molecular layer of the contralateral dentate gyrus, and CA2/CA3 pyramidal neurons send collaterals to contralateral CA3, CA2, and CA1 regions. By contrast, commissural outputs from CA1 remain largely unexplored.

Here, we show that dorsal CA1 (dCA1) pyramidal neurons located in the right hemisphere project to contralateral dorsal subiculum (dSUB) in addition to contralateral dCA1.

We then assess the function of the projection from the right dCA1 to the left dSUB and find that this interhemispheric pathway supports spatial memory and spatial working memory, two cognitive functions altered in the Df16(A)+/− mouse model of 22q11.2 deletion syndrome (22q11.2DS) associated with schizophrenia.

Notably, the right-to-left dCA1 interhemispheric projections are disrupted in Df16(A)+/− mice, suggesting that dysregulation of this circuit may contribute to 22q11.2DS-related cognitive deficits.



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