4.8 Article

Gut microbiota shapes social dominance through modulating HDAC2 in the medial prefrontal cortex

期刊

CELL REPORTS
卷 38, 期 10, 页码 -

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CELL PRESS
DOI: 10.1016/j.celrep.2022.110478

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资金

  1. National Key Basic Research Program of China [2018YFC1602204, 2018YFC1602201]
  2. National Science Foundation of China [82073592, 81773475]
  3. Open Project of Anhui Key Laboratory of Tobacco Chemistry [2021307]
  4. Fundamental Research Funds for the Central Universities [JZ2020HGTB0053, 201904e01020001]

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This study found that socially dominant rats can be distinguished from subordinates based on their intestinal microbiota. Dysbiotic rats reclaim social dominance following microbiota transplantation. Core microbes and histone deacetylase HDAC2 play crucial roles in mediating dominance determination.
Social dominance is a ubiquitous phenomenon among social animals, including humans. To date, individual attributes leading to dominance (after a contest) remain largely elusive. Here, we report that socially dominant rats can be distinguished from subordinates based on their intestinal microbiota. When dysbiosis is induced, rats are predisposed to a subordinate state, while dysbiotic rats reclaim social dominance following micro biota transplantation. Winning hosts are characterized by core microbes, a majority of which are associated with butyrate production, and the sole colonization of Clostridium butyricum is sufficient to restore dominance. Regarding molecular aspects, a histone deacetylase, HDAC2, is responsive to microbial status and mediates competition outcome; however, this occurs only in a restricted population of cells in the medial prefrontal cortex (mPFC). Furthermore, HDAC2 acts by modulating synaptic activity in mPFC. Together, these findings uncover a link between commensals and host dominance, providing insight into the gut-brain mechanisms underlying dominance determination.

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