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To date, most studies on the function of TRP channels have been performed on native primary sensory neurons (pSN) from mice. However, most of the transgenic mice that express functional TRP channels in nociceptors originate from C57BL/6J mice and show no obvious phenotypes. Here, we investigate whether the function of TRPA1, a non-neuronal TRP channel, is activated in immortalized nociceptors (i.e., 293-mTrpa1) derived from transgenic mice from an outbred mouse strain (C57BL/6J) and show that the channel is functionally active in these iPSC-derived nociceptors. By the use of electrophysiological methods, we found that pharmacological TRPA1 agonists evoke Ca2+ influx and inward currents in iPSC-derived nociceptors that are similar to native pSN. Furthermore, we 0b46394aab