Abstract
Touch sensation starts with the opening of mechanically gated activated ion channels at neuroglial endings of mechanoreceptors in the skin. The function of around half of low-threshold mechanoreceptors is dependent on the presence of the mechanically gated ion channel PIEZO2. It has been reported that particularly rapidly adapting mechanosensitive currents (RA currents) in the cell bodies of acutely cultured sensory neurons are dependent on PIEZO2. Here we re-examined this question by making a quantitative study of mechanically gated currents activated by substrate deflection in sensory neurons lacking PIEZO2. We characterized mechanically gated currents from embryonic and postnatal sensory neurons, taken from global Piezo2(-/-) or Piezo2 conditional knockouts (Piezo2(cKO)), respectively. Surprisingly, in both models, Piezo2 gene deletion was not associated with any significant reduction in the sensitivity or incidence of mechanosensitive currents compared with wild-type controls. There was, however, a moderate reduction in the incidence of RA currents with very fast activation and inactivation kinetics in both embryonic Piezo2(-/-) and juvenile Piezo2(cKO) mice. These results show that PIEZO2 channels are not the only mechanosensitive channels mediating RA currents in sensory neurons. Furthermore, our data suggest that the phenotypes associated with Piezo2 loss of function alleles may sometimes be due to secondary effects of gene deletion, for example, by changing the developmental trajectory of sensory neurons. Emphasis should be put on the diversity of mechanosensitive ion channel function in sensory neurons, which needs to be further elucidated.