Extracellular S100B alters spontaneous Ca2+ fluxes in dopaminergic neurons via L-type voltage gated calcium channels: Implications for Parkinsons disease Academic Article uri icon


  • AbstractParkinsons disease (PD) is associated with an abnormal increase in S100B within the midbrain and cerebrospinal fluid. In addition, overexpression of S100B in mice accelerates the loss of substantia nigra pars compacta (SNc) dopaminergic (DA) neurons, suggesting a role for this protein in PD pathogenesis. We found that in the mouse SNc, S100B labeled astrocytic processes completely envelop the somata of tyrosine hydroxylase (TH) positive DA neurons. Based on this finding, we rationalized that abnormal increases in extracellularly secreted S100B by astrocytic processes in the SNc could alter DA neuron activity, thereby causing dysregulated midbrain function. To test this hypothesis, we measured the effect of bath perfused S100B peptide on the frequency and amplitude of spontaneous calcium fluxes in identified TH+ and TH midbrain neurons from 3-week old mouse primary midbrain cultures. Acute exposure to 50 pM S100B caused a 2-fold increase in calcium flux frequency only in TH+ DA neurons. The L-type voltage gated calcium channel (VGCC) inhibitor, diltiazem eliminated S100B-mediated increases in DA neuron calcium flux frequency, while the T-type specific VGCC blocker mibefradil failed to inhibit the stimulatory effect of S100B. Chronic exposure to S100B caused a 3-fold reduction in calcium flux frequencies of TH+ neurons and also reduced calcium flux amplitudes in TH neurons by 4-fold. Together, our results suggest that exposure to S100B pathologically alters spontaneous calcium activity in midbrain neurons via an extracellular mechanism involving L-type VGCCs expressed in DA neurons. These findings are relevant to understanding mechanisms underlying DA neuron loss during PD.Table of Contents ImageMain PointsExtracellular S100B increases Ca2+ fluxes in dopaminergic neuronsL-type VGCCs in dopaminergic neurons are required for S100B-mediated increases in Ca2+ fluxesChronic S100B alters Ca2+ fluxes in dopaminergic and non-dopaminergic neurons

published proceedings

  • bioRxiv

altmetric score

  • 1.5

author list (cited authors)

  • Bancroft, E. A., Pandey, G., Zarate, S. M., & Srinivasan, R.

citation count

  • 0

complete list of authors

  • Bancroft, Eric A||Pandey, Gauri||Zarate, Sara M||Srinivasan, Rahul

publication date

  • January 2021