TY - JOUR
T1 - Influence of gap junctions upon Ca2+ propagation from stimulated keratinocytes to DRG neurons
AU - Seto, Chiaki
AU - Toyoda, Kenta
AU - Inada, Kousuke
AU - Oka, Kotaro
AU - Ito, Etsuro
N1 - Funding Information:
This study was supported by a Grant-in-Aid (KAKENHI) for Scientific Research (A) from the Japan Society for the Promotion of Science to K.O. and E.I. (19H00633). The funder had no role in the study design, data collection, analysis, decision to publish, or preparation of the manuscript.
Publisher Copyright:
© 2022 THE BIOPHYSICAL SOCIETY OF JAPAN.
PY - 2022
Y1 - 2022
N2 - Epidermal cells, such as keratinocytes, are regarded as the first sensory cells to transmit nociception and mechanoreception to free nerve endings extended from the dorsal root ganglion (DRG). Previous studies suggested that this transmission occurs as Ca2+ propagation via ATP receptors. Conversely, the influence of gap junctions on this Ca2+ propagation is largely unknown. Thus, we examined the localization and the role of connexin 43 among keratinocytes and DRG neurons. We co-cultured keratinocytes and DRG neurons and investigated the effect of pharmacological blockade of gap junctions on Ca2+ propagation upon stimulation of a single keratinocyte. Immunocytochemical experiments showed that connexin 43 is localized between keratinocytes and between keratinocytes and DRG neurons. Octanol, a gap junction inhibitor, significantly suppressed the concentrical Ca2+ propagation. Therefore, we conclude that the Ca2+ propagation mechanism via gap junctions from stimulated keratinocytes to free nerve endings should be taken into account.
AB - Epidermal cells, such as keratinocytes, are regarded as the first sensory cells to transmit nociception and mechanoreception to free nerve endings extended from the dorsal root ganglion (DRG). Previous studies suggested that this transmission occurs as Ca2+ propagation via ATP receptors. Conversely, the influence of gap junctions on this Ca2+ propagation is largely unknown. Thus, we examined the localization and the role of connexin 43 among keratinocytes and DRG neurons. We co-cultured keratinocytes and DRG neurons and investigated the effect of pharmacological blockade of gap junctions on Ca2+ propagation upon stimulation of a single keratinocyte. Immunocytochemical experiments showed that connexin 43 is localized between keratinocytes and between keratinocytes and DRG neurons. Octanol, a gap junction inhibitor, significantly suppressed the concentrical Ca2+ propagation. Therefore, we conclude that the Ca2+ propagation mechanism via gap junctions from stimulated keratinocytes to free nerve endings should be taken into account.
KW - connexin 43
KW - dorsal root ganglion
KW - free nerve ending
KW - octanol
KW - skin
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U2 - 10.2142/biophysico.bppb-v19.0041
DO - 10.2142/biophysico.bppb-v19.0041
M3 - Article
AN - SCOPUS:85139521454
SN - 1349-2942
VL - 19
JO - Biophysics and physicobiology
JF - Biophysics and physicobiology
M1 - e190041
ER -