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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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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•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.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2021.10.046</identifier><identifier>PMID: 34710828</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>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</subject><ispartof>Biochemical and biophysical research communications, 2021-12, Vol.582, p.131-136</ispartof><rights>2021 Elsevier Inc.</rights><rights>Copyright © 2021 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c466t-ef18a0e36bc6269792c7ebb10520d7b39bca2d745644211e156491ce5f33d16f3</citedby><cites>FETCH-LOGICAL-c466t-ef18a0e36bc6269792c7ebb10520d7b39bca2d745644211e156491ce5f33d16f3</cites><orcidid>0000-0003-4066-4867 ; 0000-0003-4614-7473</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006291X21014546$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34710828$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shindo, Yutaka</creatorcontrib><creatorcontrib>Fujita, Keigo</creatorcontrib><creatorcontrib>Tanaka, Mari</creatorcontrib><creatorcontrib>Fujio, Hiroki</creatorcontrib><creatorcontrib>Hotta, Kohji</creatorcontrib><creatorcontrib>Oka, Kotaro</creatorcontrib><title>Mechanical stimulus-evoked signal transduction between keratinocytes and sensory neurons via extracellular ATP</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><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.</description><subject>Adenosine Triphosphate - metabolism</subject><subject>Adenosine Triphosphate - pharmacology</subject><subject>Animals</subject><subject>ATP release</subject><subject>Benzofurans - analysis</subject><subject>Benzofurans - chemistry</subject><subject>Ca2+ imaging</subject><subject>Calcium - metabolism</subject><subject>Cations, Divalent</subject><subject>Cell Membrane - drug effects</subject><subject>Cell Membrane - metabolism</subject><subject>Coculture Techniques</subject><subject>DRG neurons</subject><subject>Epidermis</subject><subject>Epidermis - innervation</subject><subject>Epidermis - metabolism</subject><subject>Ganglia, Spinal - cytology</subject><subject>Ganglia, Spinal - metabolism</subject><subject>Genes, Reporter</subject><subject>Humans</subject><subject>iATPSnFR</subject><subject>Imidazoles - analysis</subject><subject>Imidazoles - chemistry</subject><subject>Infant, Newborn</subject><subject>Keratinocytes - cytology</subject><subject>Keratinocytes - drug effects</subject><subject>Keratinocytes - metabolism</subject><subject>Mechanical stimulus</subject><subject>Mechanotransduction, Cellular</subject><subject>Molecular Probes - analysis</subject><subject>Molecular Probes - chemistry</subject><subject>Nociception - physiology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Sensory Receptor Cells - cytology</subject><subject>Sensory Receptor Cells - drug effects</subject><subject>Sensory Receptor Cells - metabolism</subject><subject>Time-Lapse Imaging</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMFu1DAURa0K1E5Lf4BF5SWbDO85GWcidVNVhSIVwaJI7CzbeSmeZuzWdgbm73E0pUtWtq7OvbIPY-8RlggoP26WxkS7FCCwBEto5BFbIHRQCYTmDVsAgKxEhz9P2GlKGwDERnbH7KRuWoS1WC-Y_0r2l_bO6pGn7LbTOKWKduGRep7cgy9xjtqnfrLZBc8N5d9Enj9S1Nn5YPeZEte-0ORTiHvuaYrBJ75zmtOfUrY0jtOoI7-6__6OvR30mOj85TxjPz7d3F_fVnffPn-5vrqrbCNlrmjAtQaqpbFSyK7thG3JGISVgL41dWesFn3brGTTCETCcunQ0mqo6x7lUJ-xD4fdpxieJ0pZbV2aH6I9hSkpseoAQQqQBRUH1MaQUqRBPUW31XGvENTsWW3U7FnNnueseC6li5f9yWypf638E1uAywNA5Zc7R1El68hb6l0km1Uf3P_2_wLtapCe</recordid><startdate>20211210</startdate><enddate>20211210</enddate><creator>Shindo, Yutaka</creator><creator>Fujita, Keigo</creator><creator>Tanaka, Mari</creator><creator>Fujio, Hiroki</creator><creator>Hotta, Kohji</creator><creator>Oka, Kotaro</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4066-4867</orcidid><orcidid>https://orcid.org/0000-0003-4614-7473</orcidid></search><sort><creationdate>20211210</creationdate><title>Mechanical stimulus-evoked signal transduction between keratinocytes and sensory neurons via extracellular ATP</title><author>Shindo, Yutaka ; Fujita, Keigo ; Tanaka, Mari ; Fujio, Hiroki ; Hotta, Kohji ; Oka, Kotaro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-ef18a0e36bc6269792c7ebb10520d7b39bca2d745644211e156491ce5f33d16f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adenosine Triphosphate - metabolism</topic><topic>Adenosine Triphosphate - pharmacology</topic><topic>Animals</topic><topic>ATP release</topic><topic>Benzofurans - analysis</topic><topic>Benzofurans - chemistry</topic><topic>Ca2+ imaging</topic><topic>Calcium - metabolism</topic><topic>Cations, Divalent</topic><topic>Cell Membrane - drug effects</topic><topic>Cell Membrane - metabolism</topic><topic>Coculture Techniques</topic><topic>DRG neurons</topic><topic>Epidermis</topic><topic>Epidermis - innervation</topic><topic>Epidermis - metabolism</topic><topic>Ganglia, Spinal - cytology</topic><topic>Ganglia, Spinal - metabolism</topic><topic>Genes, Reporter</topic><topic>Humans</topic><topic>iATPSnFR</topic><topic>Imidazoles - analysis</topic><topic>Imidazoles - chemistry</topic><topic>Infant, Newborn</topic><topic>Keratinocytes - cytology</topic><topic>Keratinocytes - drug effects</topic><topic>Keratinocytes - metabolism</topic><topic>Mechanical stimulus</topic><topic>Mechanotransduction, Cellular</topic><topic>Molecular Probes - analysis</topic><topic>Molecular Probes - chemistry</topic><topic>Nociception - physiology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Sensory Receptor Cells - cytology</topic><topic>Sensory Receptor Cells - drug effects</topic><topic>Sensory Receptor Cells - metabolism</topic><topic>Time-Lapse Imaging</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shindo, Yutaka</creatorcontrib><creatorcontrib>Fujita, Keigo</creatorcontrib><creatorcontrib>Tanaka, Mari</creatorcontrib><creatorcontrib>Fujio, Hiroki</creatorcontrib><creatorcontrib>Hotta, Kohji</creatorcontrib><creatorcontrib>Oka, Kotaro</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shindo, Yutaka</au><au>Fujita, Keigo</au><au>Tanaka, Mari</au><au>Fujio, Hiroki</au><au>Hotta, Kohji</au><au>Oka, Kotaro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mechanical stimulus-evoked signal transduction between keratinocytes and sensory neurons via extracellular ATP</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2021-12-10</date><risdate>2021</risdate><volume>582</volume><spage>131</spage><epage>136</epage><pages>131-136</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>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.</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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