Young Hye Kwon, Joseph J Salvo, Nathan L Anderson, Donnisa Edmonds, Ania M Holubecki, Maya Lakshman, Kwangsun Yoo, B T Thomas Yeo, Kendrick Kay, Caterina Gratton, Rodrigo M Braga
{"title":"Situating the salience and parietal memory networks in the context of multiple parallel distributed networks using precision functional mapping.","authors":"Young Hye Kwon, Joseph J Salvo, Nathan L Anderson, Donnisa Edmonds, Ania M Holubecki, Maya Lakshman, Kwangsun Yoo, B T Thomas Yeo, Kendrick Kay, Caterina Gratton, Rodrigo M Braga","doi":"10.1016/j.celrep.2024.115207","DOIUrl":null,"url":null,"abstract":"<p><p>Brain networks serving higher cognitive functions are widely distributed across frontal and posterior association zones. Two exceptions have been the parietal memory network (PMN) and salience network (SAL), which are typically restricted to posterior (e.g., posterior cingulate and lateral parietal cortex) and anterior (medial prefrontal and anterior insular cortex) areas, respectively. Using high-resolution neuroimaging, we show that individualized estimates of the PMN extend beyond the posterior set and encompass frontal and insula regions canonically ascribed to the SAL. This suggests that the SAL and PMN form a unified network: \"SAL/PMN.\" Task-based analyses confirm that both anterior and posterior components of the SAL/PMN show recognition-related activity. Comparison of 3T and 7T data suggests that high-resolution data more readily revealed the unified network, underscoring the importance of fine-scale distinctions for veridical representation of brain networks. Importantly, the unified network better matches the expected parallel distributed network organization that is characteristic of association cortex.</p>","PeriodicalId":9798,"journal":{"name":"Cell reports","volume":"44 1","pages":"115207"},"PeriodicalIF":7.5000,"publicationDate":"2025-01-28","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.2024.115207","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/17 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Brain networks serving higher cognitive functions are widely distributed across frontal and posterior association zones. Two exceptions have been the parietal memory network (PMN) and salience network (SAL), which are typically restricted to posterior (e.g., posterior cingulate and lateral parietal cortex) and anterior (medial prefrontal and anterior insular cortex) areas, respectively. Using high-resolution neuroimaging, we show that individualized estimates of the PMN extend beyond the posterior set and encompass frontal and insula regions canonically ascribed to the SAL. This suggests that the SAL and PMN form a unified network: "SAL/PMN." Task-based analyses confirm that both anterior and posterior components of the SAL/PMN show recognition-related activity. Comparison of 3T and 7T data suggests that high-resolution data more readily revealed the unified network, underscoring the importance of fine-scale distinctions for veridical representation of brain networks. Importantly, the unified network better matches the expected parallel distributed network organization that is characteristic of association cortex.
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.