Transcriptional down-regulation of MARCKS gene expression in immortalized hippocampal cells by lithium

L Wang1, X Liu, R H Lenox

  • 1Department of Psychiatry, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.

Journal of Neurochemistry
|November 28, 2001
PubMed

Insights

Chronic lithium exposure down-regulates myristoylated alanine-rich C kinase substrate (MARCKS) protein by reducing its gene transcription. This effect involves a specific lithium-responsive region in the Macs gene promoter, impacting cytoskeletal dynamics.

Area of Science:

  • Neuroscience
  • Molecular Biology
  • Cell Biology

Background:

  • Myristoylated alanine-rich C kinase substrate (MARCKS) is crucial for actin-membrane plasticity and cytoskeletal restructuring.
  • MARCKS protein is significantly reduced in the hippocampus following long-term lithium exposure.
  • Lithium is used clinically and affects cellular processes.

Purpose of the Study:

  • To investigate the transcriptional and post-transcriptional mechanisms behind lithium-induced down-regulation of MARCKS protein.
  • To identify the specific regulatory elements in the Macs gene promoter affected by lithium.

Main Methods:

  • Cultured immortalized hippocampal cells (HN33.dw) were exposed to lithium.
  • MARCKS mRNA and protein levels were measured.
  • Nuclear run-off assays assessed mRNA transcription.
  • Promoter activity was analyzed using transient transfection with wild-type and mutant mouse Macs promoter constructs.

Main Results:

  • Chronic lithium exposure reduced both MARCKS mRNA and protein levels concurrently.
  • MARCKS mRNA stability was unaffected, but transcription decreased by approximately 50%.
  • Lithium attenuated Macs promoter activity after 7-10 days, dependent on a specific 280-bp region (-993 to -713 bp), identified as the lithium-responsive region (LRR).

Conclusions:

  • Lithium-induced down-regulation of MARCKS protein in hippocampal cells is primarily mediated by transcriptional inhibition of the Macs gene.
  • A specific promoter region (LRR) is critical for this lithium-induced repression, suggesting interference with transcriptional activators.