辣椒对Cav2.2通道的动态控制

IF 5.1 Q2 CELL BIOLOGY
Paz Duran, Rajesh Khanna
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Capsaicin has been utilized as a tool to study the regulation of pain since TRPV1 channels have been reported to be crucial for heat nociception.1 Despite reports that capsaicin binding to TRPV1 channels causes pain, it has been demonstrated that prolonged exposures to capsaicin can desensitize dorsal root ganglion (DRG) neurons, thus reducing afferent drive and reducing synaptic transmission in the dorsal horn.2 Several studies have established that voltage-gated calcium channels (VGCCs) are key modulators of nociceptive and nociplastic pain.3 VGCCs are transmembrane proteins composed of a principal pore-forming α subunit that mediates Ca2+ entry into the cell in response to membrane potential changes. Based on their biophysical characteristics, VGCCs are classified into low voltage activated (LVA) and high voltage activated (HVA) families. HVA channels are typically expressed with auxiliary subunits β and α2δ that regulate the trafficking and function of these channels. 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Some Like It Hot: Dynamic Control of Cav2.2 Channels By Chili Peppers.

Some Like It Hot: Dynamic Control of Cav2.2 Channels By Chili Peppers.
Spicy meals causes the production of happy endorphins together with the triggering of heat and pain, similar to a runner’s high. The active ingredient in hot chili peppers that causes their distinctive burning sensation is called capsaicin (8-methylN-vanillyl-6-nonenamide). This bioactive substance binds to the primary afferent neurons’ transient receptor potential vanilloid 1 (TRPV1) cation channels, which when activated, cause a sensation of heat. Capsaicin has been utilized as a tool to study the regulation of pain since TRPV1 channels have been reported to be crucial for heat nociception.1 Despite reports that capsaicin binding to TRPV1 channels causes pain, it has been demonstrated that prolonged exposures to capsaicin can desensitize dorsal root ganglion (DRG) neurons, thus reducing afferent drive and reducing synaptic transmission in the dorsal horn.2 Several studies have established that voltage-gated calcium channels (VGCCs) are key modulators of nociceptive and nociplastic pain.3 VGCCs are transmembrane proteins composed of a principal pore-forming α subunit that mediates Ca2+ entry into the cell in response to membrane potential changes. Based on their biophysical characteristics, VGCCs are classified into low voltage activated (LVA) and high voltage activated (HVA) families. HVA channels are typically expressed with auxiliary subunits β and α2δ that regulate the trafficking and function of these channels. The N-type calcium channel, also known as CaV2.2, is a member of the HVA family that is expressed at high levels in sensory neurons where they are key mediators of neurotransmitter release and the transmission of sensory information from the periphery to central sites.4 Given that CaV2.2 channels are the main presynaptic VGCCs and have a critical role in regulating nociceptive transmission, it is reasonable to predict a regulation mediated by capsaicin and TRPV1. However, little is known about the underlying mechanisms of the functional interaction between these channels and their presynaptic function. This gap in knowledge was explored in a very ingenious way by Krishma Ramgoolam and Annette Dolphin in a new study reported in this issue of FUNCTION.5The authors build on their long-standing expertise of N-type calcium channels (CaV2.2) to investigate their functional presynaptic expression and explore their interaction with TRPV1 channels in primary nociceptors. Here, the Dolphin group used their previously described CaV2.2 HA knock-in mouse line, which expresses CaV2.2 with a hemagglutinin (HA) exofacial epitope tag to easily localize endogenous CaV2.2 channels.5 Using co-cultures of DRG neurons isolated from CaV2.2 HA knock-in mice with spinal cord neurons from wild-type (WT) mice and approaches, including immunofluorescence staining and calcium imaging, this study investigated the neuronal maturation, synapse formation, distribution, and presynaptic function of the tagged Ntype calcium channels. First, CaV2.2 localization during neuronal maturation and synapse formation was explored using immunofluorescence staining. CaV2.2 HA expression over time showed a decrease in cell surface expression at the cell body of DRG neurons that was accompanied by a commensurate significant increase at presynaptic terminals. The authors then extended the characterization of the development of CaV2.2 HA expression at presynaptic boutons using super-resolution microscopy and found that, in mature cultures, the channels were closely juxtaposed to synaptic markers Homer, RIM 1/2 and vGlut2, suggesting the formation of mature synapses. Next, using live-cell calcium imaging
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CiteScore
5.70
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