Journal Article

Cold sensing by Na V 1.8-positive and Na V 1.8-negative sensory neurons

Millet, Q., Sikandar, S., Santana-Varela, S., MacDonald, D. I., Emery, E. C., Wood, J. N., Luiz, A. P.

2019

Overview

The cellular correlate for cold sensing has been ascribed to either Trpm8-expressing or Na V 1.8-expressing neurons. Importantly, transcriptomic analysis shows that these neuronal populations are nonoverlapping. Using in vivo GCaMP imaging in live mice we show that the vast majority of acute cold-sensing neurons activated at ≥1 °C do not express Na V 1.8, and that the loss of Na V 1.8 does not affect acute cold-sensing behavior in mice. Instead, we show that cold-responding neurons are enriched with Trpm8 as well as numerous potassium channels, including Kcnk9. By contrast, Na V 1.8-positive neurons signal prolonged extreme cold. These observations highlight the complexity of cold sensing in DRG neurons, and the role of Na V 1.8-negative neurons in cold sensing down to 1 °C. The ability to detect environmental cold serves as an important survival tool. The sodium channels Na V 1.8 and Na V 1.9, as well as the TRP channel Trpm8, have been shown to contribute to cold sensation in mice. Surprisingly, transcriptional profiling shows that Na V 1.8/Na V 1.9 and Trpm8 are expressed in nonoverlapping neuronal populations. Here we have used in vivo GCaMP3 imaging to identify cold-sensing populations of sensory neurons in live mice. We find that ∼80% of neurons responsive to cold down to 1 °C do not express Na V 1.8, and that the genetic deletion of Na V 1.8 does not affect the relative number, distribution, or maximal response of cold-sensitive neurons. Furthermore, the deletion of Na V 1.8 had no observable effect on transient cold-induced (≥5 °C) behaviors in mice, as measured by the cold-plantar, cold-plate (5 and 10 °C), or acetone tests. In contrast, nocifensive-like behavior to extreme cold-plate stimulation (−5 °C) was completely absent in mice lacking Na V 1.8. Fluorescence-activated cell sorting (FACS) and subsequent microarray analysis of sensory neurons activated at 4 °C identified an enriched repertoire of ion channels, which include the Trp channel Trpm8 and potassium channel Kcnk9, that are potentially required for cold sensing above freezing temperatures in mouse DRG neurons. These data demonstrate the complexity of cold-sensing mechanisms in mouse sensory neurons, revealing a principal role for Na V 1.8-negative neurons in sensing both innocuous and acute noxious cooling down to 1 °C, while Na V 1.8-positive neurons are likely responsible for the transduction of prolonged extreme cold temperatures, where tissue damage causes pan-nociceptor activation.

• Subject: Animals / Cold Temperature / Ganglia, Spinal - diagnostic imaging / Ganglia, Spinal - metabolism / Ganglia, Spinal - physiology / Mice / NAV1.8 Voltage-Gated Sodium Channel - genetics / Nociceptors - metabolism / Nociceptors - physiology / Potassium Channels - genetics / Sensory Receptor Cells - metabolism / Sensory Receptor Cells - physiology / Thermosensing - genetics / TRPM Cation Channels - genetics