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Stromal‐cell‐derived factor 1α /CXCL12 modulates high‐threshold calcium currents in rat substantia nigra
Author(s) -
Guyon A.,
Skrzydelski D.,
Rovère C.,
Apartis E.,
Rostène W.,
Kitabgi P.,
Mélik Parsadaniantz S.,
Nahon J. L.
Publication year - 2008
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1111/j.1460-9568.2008.06367.x
Subject(s) - substantia nigra , dopaminergic , chemistry , dopamine , neuroscience , microbiology and biotechnology , medicine , endocrinology , biology
Dopaminergic neurons of the substantia nigra constitutively express the CXCR4 receptor for the chemokine stromal‐cell‐derived factor 1α (CXCL12) but, to date, no direct effect of CXCR4 activation by CXCL12 on membrane conductance of dopaminergic neurons has been demonstrated. We tested the effects of CXCL12 on whole‐cell currents of dopaminergic neurons recorded in patch clamp in substantia nigra slices and showed that CXCL12 (0.01–10 n m ) increased the amplitude of total high‐voltage‐activated (HVA) Ca currents through CXCR4 activation. This effect was reversibly reduced by ϖ‐conotoxin‐GVIA, suggesting that CXCL12 acted on N‐type Ca currents, known to be involved in dopamine (DA) release. We therefore investigated the effects of CXCL12 on DA release from cultured dopaminergic neurons from the rat mesencephalon. In basal conditions, CXCL12 alone had no effect on DA release. When neurons were depolarized with KCl (20 m m ), and thus when HVA Ca currents were activated, low CXCL12 concentrations (1–50 n m ) increased DA release via CXCR4 stimulation. These data strongly suggest that the chemokine CXCL12 can act directly as a neuromodulator of dopaminergic neuronal electrical activity through the modulation of HVA currents.