Key result
Inhibition of KV7/KCNQ channels by XE991 or TEA significantly promoted the motility of rat primary cultured oligodendrocyte progenitor cells in vitro (p<0.01).
KV7/KCNQ channels are functionally expressed in oligodendrocyte progenitor cells and their inhibition promotes cell motility, suggesting a role in OPC function.
BACKGROUND: K(V)7/KCNQ channels are widely expressed in neurons and they have multiple important functions, including control of excitability, spike afterpotentials, adaptation, and theta resonance. Mutations in KCNQ genes have been demonstrated to associate with human neurological pathologies. However, little is known about whether K(V)7/KCNQ channels are expressed in oligodendrocyte lineage cells (OLCs) and what their functions in OLCs. METHODS AND FINDINGS: In this study, we characterized K(V)7/KCNQ channels expression in rat primary cultured OLCs by RT-PCR, immunostaining and electrophysiology. KCNQ2-5 mRNAs existed in all three developmental stages of rat primary cultured OLCs. K(V)7/KCNQ proteins were also detected in oligodendrocyte progenitor cells (OPCs, early developmental stages of OLCs) of rat primary cultures and cortex slices. Voltage-clamp recording revealed that the I(M) antagonist XE991 significantly reduced K(V)7/KCNQ channel current (I(K(Q))) in OPCs but not in differentiated oligodendrocytes. In addition, inhibition of K(V)7/KCNQ channels promoted OPCs motility in vitro. CONCLUSIONS: These findings showed that K(V)7/KCNQ channels were functionally expressed in rat primary cultured OLCs and might play an important role in OPCs functioning in physiological or pathological conditions.
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Wang et al. (2011) studied Oligodendrocyte progenitor cell function (basic science). KV7/KCNQ channel inhibitors (XE991 and TEA) vs. Control (no inhibitor) was evaluated on Oligodendrocyte progenitor cell motility (number of migrated cells) (p=<0.01). Inhibition of KV7/KCNQ channels by XE991 or TEA significantly promoted the motility of rat primary cultured oligodendrocyte progenitor cells in vitro (p<0.01).
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