{"title":"Gamma synchronization between the medial temporal lobe and medial frontal cortex for goal-directed visual attention in humans.","authors":"Jie Zhang, Jing Xia, Huihui Zhou, Shuo Wang","doi":"10.1016/j.celrep.2025.115905","DOIUrl":null,"url":null,"abstract":"<p><p>Goal-directed visual attention is a fundamental cognitive function that engages multiple brain regions, yet the neural circuit mechanisms in humans remain unclear. We addressed this question by simultaneously recording neural activity from the medial temporal lobe (MTL) and medial frontal cortex (MFC) during a goal-directed visual search task. We found that gamma-band synchronization between the MTL and MFC signaled target detection. Using two additional tasks, we dissociated the neural processes underlying working memory and search decision execution, revealing distinct patterns of synchronization. Further analyses showed that dorsal anterior cingulate cortex (dACC) spike-MTL LFP synchronization encoded search dynamics and contributed to guiding behavior. Importantly, MTL-MFC synchronization disproportionately modulated neural representational geometry, highlighting its impact on information encoding. Finally, we demonstrated directional gamma influences across brain areas and cross-frequency coupling. Together, these findings illuminate the circuit-level dynamics underlying visual attention and offer insights into how the human brain selectively processes information in complex visual environments.</p>","PeriodicalId":9798,"journal":{"name":"Cell reports","volume":"44 7","pages":"115905"},"PeriodicalIF":6.9000,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell reports","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.celrep.2025.115905","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/25 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Goal-directed visual attention is a fundamental cognitive function that engages multiple brain regions, yet the neural circuit mechanisms in humans remain unclear. We addressed this question by simultaneously recording neural activity from the medial temporal lobe (MTL) and medial frontal cortex (MFC) during a goal-directed visual search task. We found that gamma-band synchronization between the MTL and MFC signaled target detection. Using two additional tasks, we dissociated the neural processes underlying working memory and search decision execution, revealing distinct patterns of synchronization. Further analyses showed that dorsal anterior cingulate cortex (dACC) spike-MTL LFP synchronization encoded search dynamics and contributed to guiding behavior. Importantly, MTL-MFC synchronization disproportionately modulated neural representational geometry, highlighting its impact on information encoding. Finally, we demonstrated directional gamma influences across brain areas and cross-frequency coupling. Together, these findings illuminate the circuit-level dynamics underlying visual attention and offer insights into how the human brain selectively processes information in complex visual environments.
期刊介绍:
Cell Reports publishes high-quality research across the life sciences and focuses on new biological insight as its primary criterion for publication. The journal offers three primary article types: Reports, which are shorter single-point articles, research articles, which are longer and provide deeper mechanistic insights, and resources, which highlight significant technical advances or major informational datasets that contribute to biological advances. Reviews covering recent literature in emerging and active fields are also accepted.
The Cell Reports Portfolio includes gold open-access journals that cover life, medical, and physical sciences, and its mission is to make cutting-edge research and methodologies available to a wide readership.
The journal's professional in-house editors work closely with authors, reviewers, and the scientific advisory board, which consists of current and future leaders in their respective fields. The advisory board guides the scope, content, and quality of the journal, but editorial decisions are independently made by the in-house scientific editors of Cell Reports.