Key result
Egr-1 knockdown significantly decreased Ca2+ currents in dorsal root ganglion neurons, while its overexpression increased Ca2+ currents in the F11 cell line.
The transcription factor Egr-1 regulates the expression of the CaVα2δ-1 subunit and modulates Ca2+ currents, providing insight into mechanisms potentially relevant to neuropathic pain.
Egr-1 regulation of CaVα2δ may alter channel density in neuropathic pain; leaves open therapeutic targeting pending validation.
It is well known that the CaVα2δ auxiliary subunit regulates the density of high voltage-activated Ca2+ channels in the plasma membrane and that alterations in their functional expression might have implications in the pathophysiology of diverse human diseases such as neuropathic pain. However, little is known concerning the transcriptional regulation of this protein. We previously characterized the promoter of CaVα2δ, and here we report its regulation by the transcription factor Egr-1. Using the neuroblastoma N1E-115 cells, we found that Egr-1 interacts specifically with its binding site in the promoter, affecting the transcriptional regulation of CaVα2δ. Overexpression and knockdown analysis of Egr-1 showed significant changes in the transcriptional activity of the CaVα2δ promoter. Egr-1 also regulated the expression of CaVα2δ at the level of protein. Also, functional studies showed that Egr-1 knockdown significantly decreases Ca2+ currents in dorsal root ganglion (DRG) neurons, while overexpression of the transcription factor increased Ca2+ currents in the F11 cell line, a hybrid of DRG and N18TG2 neuroblastoma cells. Studying the effects of Egr-1 on the transcriptional expression of CaVα2δ could help to understand the regulatory mechanisms of this protein in both health and disease.
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González‐Ramírez et al. (2018) studied this question. Egr-1 overexpression and knockdown was evaluated on Transcriptional activity of CaVα2δ promoter and Ca2+ currents. Egr-1 knockdown significantly decreased Ca2+ currents in dorsal root ganglion neurons, while its overexpression increased Ca2+ currents in the F11 cell line.
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