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Inhibition of c-Jun in AgRP neurons increases stress-induced anxiety and colitis susceptibility

  • Fuxin Jiao
  • , Xiaoming Hu
  • , Hanrui Yin
  • , Feixiang Yuan
  • , Ziheng Zhou
  • , Wei Wu
  • , Shanghai Chen
  • , Zhanju Liu*
  • , Feifan Guo*
  • *Corresponding author for this work
  • Fudan University
  • CAS - Shanghai Institute of Nutrition and Health
  • Tongji University

Research output: Contribution to journalArticlepeer-review

Abstract

Psychiatric disorders, such as anxiety, are associated with inflammatory bowel disease (IBD), however, the neural mechanisms regulating this comorbidity are unknown. Here, we show that hypothalamic agouti-related protein (AgRP) neuronal activity is suppressed under chronic restraint stress (CRS), a condition known to increase anxiety and colitis susceptibility. Consistently, chemogenic activation or inhibition of AgRP neurons reverses or mimics CRS-induced increase of anxiety-like behaviors and colitis susceptibility, respectively. Furthermore, CRS inhibits AgRP neuronal activity by suppressing the expression of c-Jun. Moreover, overexpression of c-Jun in these neurons protects against the CRS-induced effects, and knockdown of c-Jun in AgRP neurons (c-Jun∆AgRP) promotes anxiety and colitis susceptibility. Finally, the levels of secreted protein thrombospondin 1 (THBS1) are negatively associated with increased anxiety and colitis, and supplementing recombinant THBS1 rescues colitis susceptibility in c-Jun∆AgRP mice. Taken together, these results reveal critical roles of hypothalamic AgRP neuron-derived c-Jun in orchestrating stress-induced anxiety and colitis susceptibility.

Original languageEnglish
Article number50
JournalCommunications Biology
Volume6
Issue number1
DOIs
StatePublished - Dec 2023
Externally publishedYes

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