Changed PGA and POSTN levels in choroid plexus are associated with depressive-like behaviors in mice

Jie Liu1, Yong He1, Ke Cheng1

  • 1Chongqing Key Laboratory of Neurobiology, Chongqing, 400016, China; Institute of Neuroscience and the Collaborative Innovation Center for Brain Science, Chongqing Medical University, Chongqing, 400016, China.

Insights

Major depressive disorder (MDD) may involve specific proteins like Pepsin A (PGA) and periostin (POSTN). Their expression in the brain's choroid plexus (CP) could be a key factor in MDD pathogenesis.

Area of Science:

  • Neuroscience
  • Biochemistry
  • Psychiatry

Background:

  • Major depressive disorder (MDD) is a leading cause of global disability.
  • Cerebrospinal fluid (CSF) proteins are increasingly recognized as potential biomarkers for MDD.
  • The choroid plexus (CP) produces CSF and interfaces with brain tissue, reflecting its metabolic state.

Purpose of the Study:

  • To investigate the expression of Pepsin A (PGA) and periostin (POSTN) in the CP of mice.
  • To compare PGA and POSTN expression between lipopolysaccharide (LPS)-induced MDD models and wild-type (WT) mice.
  • To explore the potential role of CP-expressed PGA and POSTN in MDD pathogenesis.

Main Methods:

  • Utilized a lipopolysaccharide (LPS)-induced mouse model to mimic MDD.
  • Examined protein expression levels of PGA and POSTN within the choroid plexus (CP).
  • Compared protein expression between MDD model mice and wild-type controls.

Main Results:

  • Observed discrepancies in PGA and POSTN expression in the CP between LPS-induced MDD mice and WT mice.
  • These findings suggest altered expression of specific proteins in the CP during depression-like states.
  • PGA and POSTN identified as potential candidates involved in MDD.

Conclusions:

  • Expression of Pepsin A (PGA) and periostin (POSTN) in the choroid plexus (CP) may be implicated in the pathogenesis of Major Depressive Disorder (MDD).
  • These proteins could serve as novel targets for understanding and treating MDD.
  • Further research into CP protein expression may enhance diagnostic and therapeutic strategies for MDD.

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