Hiring in life sciences? Share your open positions with our professional community. Read more Close

Advertisement

ULK1 inhibits depressive behaviours by reversing RYR2-mediated hyperactivity in lateral habenula.

Created on 09 Sep 2026

Authors

Pingjie Wang, Xiaohan Tong, Yun Liu, Junfeng Li, Shilin He, Yanhua Huang, Ruijia Ma, Boya Huang, Wenghei Hong, Ruizhe Sun, Nikias Siafarikas, Tormod Fladby, He-Ling Wang, Oscar Junhong Luo, Qian Wang, Yuchao Li, Ji-Chun Zhang, Lu Huang, Chaoran Ren, Guobing Chen, Evandro Fei Fang, Song Lin

Published in

Brain : a journal of neurology. Sep 09, 2026. Epub Sep 09, 2026.

Abstract

Research has implicated disrupted autophagy initiation in the pathophysiology of depression. However, the role of Unc-51-like Kinase 1 (ULK1), a key regulator of autophagy initiation, in depression remains poorly understood. Here, using behavioural, molecular, and genetic approaches, we show that serum ULK1 levels are decreased in both patients with depression and mice susceptible to chronic social-defeat stress, and that both ULK1 and p-ULK1 (Ser-555) are downregulated in the lateral habenula (LHb) of susceptible mice. In addition, ULK1 deficiency in the LHb is sufficient to induce depressive-like behaviours in mice. Conversely, restoration of ULK1 in the LHb, either genetically or pharmacologically, produced antidepressant-like effects. Moreover, ULK1 deficiency specifically in LHb glutamatergic neurons induces neuronal hyperactivity, which contributes to ULK1 deficiency-induced depressive-like behaviours. Mechanistically, LHb glutamatergic neuron-specific ULK1 deficiency upregulates ryanodine receptor 2 (RYR2), which mediates increased stress-evoked presynaptic calcium transients, enhances presynaptic glutamatergic transmission, and neuronal hyperactivity in the LHb, ultimately resulting in depressive-like behaviours. Collectively, our findings suggest that ULK1 deficiency in LHb glutamatergic neurons may contribute to the development and progression of depression and identify ULK1 as a potential target for further investigation in antidepressant therapy development.

PMID:
42714059
Bibliographic data and abstract were imported from PubMed on 09 Sep 2026.

Read full publication at:
Please sign in to see all details.

Advertisement

Stats

  • Community rating n/a 0 votes
  • Reviewers' rating n/a 0 votes
  • Your rating

1-terrible, 9-excellent. How would you rate this publication? Sign in in to submit your rating.

  • Recommendations n/a n/a positive of 0 vote(s)
  • Views 17
  • Comments 0

Recommended by

  • No recommendations yet.

Post a comment

You need to be signed in to post comments. You can sign in here.

Comments

There are no comments yet.

Advertisement