Neuronal TCF7L2 in Lateral Habenula Is Involved in Stress-Induced Depression

Int J Mol Sci. 2024 Nov 19;25(22):12404. doi: 10.3390/ijms252212404.

Abstract

Depression is a complex psychiatric disorder that has substantial implications for public health. The lateral habenula (LHb), a vital brain structure involved in mood regulation, and the N-methyl-D-aspartate receptor (NMDAR) within this structure are known to be associated with depressive behaviors. Recent research has identified transcription factor 7-like 2 (TCF7L2) as a crucial transcription factor in the Wnt signaling pathway, influencing diverse neuropsychiatric processes. In this study, we explore the role of TCF7L2 in the LHb and its effect on depressive-like behaviors in mice. By using behavioral tests, AAV-mediated gene knockdown or overexpression, and pharmacological interventions, we investigated the effects of alterations in TCF7L2 expression in the LHb. Our results indicate that TCF7L2 expression is reduced in neurons within the LHb of male ICR mice exposed to chronic mild stress (CMS), and neuron-specific knockdown of TCF7L2 in LHb neurons leads to notable antidepressant activity, as evidenced by reduced immobility time in the tail suspension test (TST) and forced swimming test (FST). Conversely, the overexpression of TCF7L2 in LHb neurons induces depressive behaviors. Furthermore, the administration of the NMDAR agonist NMDA reversed the antidepressant activity of TCF7L2 knockdown, and the NMDAR antagonist memantine alleviated the depressive behaviors induced by TCF7L2 overexpression, indicating the involvement of NMDAR. These findings offer novel insights into the molecular mechanisms of depression, highlighting the potential of TCF7L2 as both a biomarker and a therapeutic target for depression. Exploring the relationship between TCF7L2 signaling and LHb function may lead to innovative therapeutic approaches for alleviating depressive symptoms.

Keywords: N-methyl-D-aspartate receptor; chronic mild stress; depression; lateral habenula; transcription factor 7-like 2.

MeSH terms

  • Animals
  • Behavior, Animal
  • Depression* / etiology
  • Depression* / metabolism
  • Disease Models, Animal
  • Gene Knockdown Techniques
  • Habenula* / metabolism
  • Male
  • Mice
  • Mice, Inbred ICR*
  • Neurons* / metabolism
  • Receptors, N-Methyl-D-Aspartate / genetics
  • Receptors, N-Methyl-D-Aspartate / metabolism
  • Stress, Psychological* / metabolism
  • Transcription Factor 7-Like 2 Protein* / genetics
  • Transcription Factor 7-Like 2 Protein* / metabolism

Substances

  • Transcription Factor 7-Like 2 Protein
  • Tcf7l2 protein, mouse
  • Receptors, N-Methyl-D-Aspartate