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Sadler, K. E.

Publications and source records attributed to Sadler, K. E..

3 recordsLinked to original sources

Piezo1 Mediates Keratinocyte Mechanotransduction

Epidermal keratinocytes mediate touch sensation by detecting and encoding tactile information to sensory neurons. However, the specific mechanotransducers that enable keratinocytes to respond to mechanical stimulation are unknown. Here, we found that the mechanically-gated ion channel Piezo1 is the major keratinocyte mechanotransducer. Keratinocyte expression of Piezo1 is critical for normal sensory afferent firing and behavioral responses to mechanical stimuli.

neuroscience

Transient receptor potential canonical 5 (TRPC5) mediates inflammatory mechanical pain

Persistent tactile pain is a poorly managed symptom of inflammatory and neuropathic injury. To develop therapies for this maladaptive sensation, the underlying molecular mediators must be identified. Using knockout mice and pharmacological inhibitors, we identified transient receptor canonical 5 (TRPC5) as a key contributor to the persistent tactile pain that occurs in many inflammatory and neuropathic preclinical rodent models. TRPC5 inhibition was effective in injuries associated with elevated levels of the bioactive phospholipid lysophosphatidylcholine (LPC). Exogenous application of LPC induced TRPC5-dependent behavioral mechanical allodynia, neuronal mechanical hypersensitivity, and spontaneous pain. In vitro, LPC activated both homomeric mouse and human TRPC5 channels, which upon examination of human dorsal root ganglia tissue, were expressed in 75% of human sensory neurons. Based on these results, TRPC5 inhibitors should be pursued as personalized therapy for spontaneous and tactile pain in conditions where elevated LPC is a biomarker.

neuroscience

Keratinocytes are required for normal cold and heat sensation

Keratinocytes are the most abundant cell type in the epidermis, the most superficial layer of the skin. Historically, epidermal-innervating sensory neurons were thought to be the exclusive detectors and transmitters of environmental stimuli. However, recent work from our lab and others has demonstrated that keratinocytes are also critical for normal mechanotransduction and mechanically-evoked behavioral responses in mice. Here, we asked whether keratinocyte activity is also required for normal cold and heat sensation. We first observed cold-induced activity in mouse, rat, hibernating 13-lined ground squirrel, and human keratinocytes and determined that keratinocyte cold activity is conserved across mammalian species. Next, using transgenic mouse tissues and pharmacological tools, we determined that keratinocyte cold responses require the release of intracellular calcium through one or more unknown cold-sensitive proteins. This cold-induced keratinocyte activity is required for normal cold sensation as optogenetic inhibition of epidermal cells reduced reflexive behavioral responses to cold stimuli. Keratinocyte inhibition also decreased reflexive behavioral responses to heat stimuli. Lastly, we demonstrated that epidermal ATP-P2X4 signaling is required for normal cold and heat sensation. Based on these data and our previous findings, keratinocyte purinergic signaling is a modality-conserved amplification system that is required for normal somatosensation in vivo.

neuroscience