Mechanical stimulus-evoked signal transduction between keratinocytes and sensory neurons via extracellular ATP

The skin is exposed to various external stimuli. Keratinocytes, which are the main cell type in the epidermis, interact with peripheral sensory neurons and modulate neuronal activity. Recent studies have revealed that keratinocytes play crucial roles in nociception, and that ATP is one of the main m...

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Veröffentlicht in:Biochemical and biophysical research communications 2021-12, Vol.582, p.131-136
Hauptverfasser: Shindo, Yutaka, Fujita, Keigo, Tanaka, Mari, Fujio, Hiroki, Hotta, Kohji, Oka, Kotaro
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container_title Biochemical and biophysical research communications
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creator Shindo, Yutaka
Fujita, Keigo
Tanaka, Mari
Fujio, Hiroki
Hotta, Kohji
Oka, Kotaro
description The skin is exposed to various external stimuli. Keratinocytes, which are the main cell type in the epidermis, interact with peripheral sensory neurons and modulate neuronal activity. Recent studies have revealed that keratinocytes play crucial roles in nociception, and that ATP is one of the main mediators of signal transduction from keratinocytes to sensory neurons. However, no quantitative cellular level analyses of ATP-mediated information flow from keratinocytes to sensory dorsal root ganglion (DRG) neurons have been conducted. In this study, we performed simultaneous imaging of cell surface ATP and intracellular Ca2+ signals using both iATPSnFR, a genetically encoded ATP probe localized to the outside of the cell membrane, and the Ca2+ probe, Fura-red. Upon mechanical stimulation of the keratinocyte with a glass needle, an increase in Ca2+ and ATP release were observed around the stimulated area, and these phenomena were positively correlated. In cultured DRG neurons and keratinocytes neighboring the stimulated keratinocyte, increased intracellular Ca2+ concentration and levels of cell surface ATP on the side closer to the stimulated cell were detected. The ratio of Ca2+ response to input ATP signal was significantly larger in DRG neurons than in keratinocytes. We found that DRG neurons were more sensitive to ATP than keratinocytes, and therefore, only DRG neurons responded to ATP at 1 μM or lower concentrations when in co-culture with keratinocytes. Moreover, signals caused by moderate mechanical stimulation of keratinocytes were transmitted predominantly to DRG neurons. These findings would be important in the further determination of the detailed mechanism of nociception in the epidermis. •Mechanical stimuli evoke ATP release only at the stimulation site in keratinocytes.•ATP release and Ca2+ signaling are positively correlated in the stimulated area.•DRG neurons are more sensitive to ATP than keratinocytes.•Information about moderate stimuli is transmitted only to DRG neurons.
doi_str_mv 10.1016/j.bbrc.2021.10.046
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Keratinocytes, which are the main cell type in the epidermis, interact with peripheral sensory neurons and modulate neuronal activity. Recent studies have revealed that keratinocytes play crucial roles in nociception, and that ATP is one of the main mediators of signal transduction from keratinocytes to sensory neurons. However, no quantitative cellular level analyses of ATP-mediated information flow from keratinocytes to sensory dorsal root ganglion (DRG) neurons have been conducted. In this study, we performed simultaneous imaging of cell surface ATP and intracellular Ca2+ signals using both iATPSnFR, a genetically encoded ATP probe localized to the outside of the cell membrane, and the Ca2+ probe, Fura-red. Upon mechanical stimulation of the keratinocyte with a glass needle, an increase in Ca2+ and ATP release were observed around the stimulated area, and these phenomena were positively correlated. In cultured DRG neurons and keratinocytes neighboring the stimulated keratinocyte, increased intracellular Ca2+ concentration and levels of cell surface ATP on the side closer to the stimulated cell were detected. The ratio of Ca2+ response to input ATP signal was significantly larger in DRG neurons than in keratinocytes. We found that DRG neurons were more sensitive to ATP than keratinocytes, and therefore, only DRG neurons responded to ATP at 1 μM or lower concentrations when in co-culture with keratinocytes. Moreover, signals caused by moderate mechanical stimulation of keratinocytes were transmitted predominantly to DRG neurons. These findings would be important in the further determination of the detailed mechanism of nociception in the epidermis. •Mechanical stimuli evoke ATP release only at the stimulation site in keratinocytes.•ATP release and Ca2+ signaling are positively correlated in the stimulated area.•DRG neurons are more sensitive to ATP than keratinocytes.•Information about moderate stimuli is transmitted only to DRG neurons.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>34710828</pmid><doi>10.1016/j.bbrc.2021.10.046</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0003-4066-4867</orcidid><orcidid>https://orcid.org/0000-0003-4614-7473</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adenosine Triphosphate - metabolism
Adenosine Triphosphate - pharmacology
Animals
ATP release
Benzofurans - analysis
Benzofurans - chemistry
Ca2+ imaging
Calcium - metabolism
Cations, Divalent
Cell Membrane - drug effects
Cell Membrane - metabolism
Coculture Techniques
DRG neurons
Epidermis
Epidermis - innervation
Epidermis - metabolism
Ganglia, Spinal - cytology
Ganglia, Spinal - metabolism
Genes, Reporter
Humans
iATPSnFR
Imidazoles - analysis
Imidazoles - chemistry
Infant, Newborn
Keratinocytes - cytology
Keratinocytes - drug effects
Keratinocytes - metabolism
Mechanical stimulus
Mechanotransduction, Cellular
Molecular Probes - analysis
Molecular Probes - chemistry
Nociception - physiology
Rats
Rats, Wistar
Sensory Receptor Cells - cytology
Sensory Receptor Cells - drug effects
Sensory Receptor Cells - metabolism
Time-Lapse Imaging
title Mechanical stimulus-evoked signal transduction between keratinocytes and sensory neurons via extracellular ATP
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