Developmental exposure to chlorpyrifos causes neuroinflammation via necroptosis in mouse hippocampus and human microglial cell line
Neurodevelopmental exposure to chlorpyrifos (CPF) could increase risks for neurological disorders, such as autism spectrum disorder, cognitive impairment, or attention deficit hyperactivity disorder. The potential involvement of microglia reactive to inflammatory stimuli in these neurological disord...
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Veröffentlicht in: | Environmental pollution (1987) 2022-12, Vol.314, p.120217-120217, Article 120217 |
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description | Neurodevelopmental exposure to chlorpyrifos (CPF) could increase risks for neurological disorders, such as autism spectrum disorder, cognitive impairment, or attention deficit hyperactivity disorder. The potential involvement of microglia reactive to inflammatory stimuli in these neurological disorders has been generally reported. However, the concrete effects and potential mechanisms of microglia dysfunction triggered by developmental CPF exposure remain unclear. Therefore, we established mouse and human embryonic microglial cells (HMC3 cell) models of developmental CPF exposure to evaluate the effects of developmental CPF exposure on neuroinflammation and underlying mechanisms. The results showed that developmental exposure to CPF enhanced the expression of Iba1 in hippocampus. CPF treatment increased inflammatory cytokines levels and TSPO expression in hippocampus and HMC3 cells. The levels of necroptosis and necroptosis-related signaling RIPK/MLKL were increased in hippocampus and HMC3 cells following CPF exposure. Furthermore, the expression of TLR4/TRIF signaling was increased in hippocampus and HMC3 cells subjected to CPF exposure. Notably, the increased levels of TLR4/TRIF signaling, RIPK/MLKL signaling, necroptosis and pro-inflammatory cytokines induced by CPF treatment were remarkably inhibited by TAK-242 (a specific TLR4 inhibitor). Additionally, the necroptosis and pro-inflammatory cytokines production induced by CPF treatment were significantly relieved by Nec-1 (a specific RIPK1 inhibitor). In general, the above results suggested that activated microglia in hippocampus subjected to developmental CPF exposure underwent RIPK1/MLKL-mediated necroptosis regulated by TLR4/TRIF signaling.
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•Developmental Chlorpyrifos exposure increases pro-inflammatory cytokine production in hippocampus.•Chlorpyrifos-induced necroptosis is involved in activation of microglia.•Developmental CPF exposure causes microglia activation in hippocampus by TLR4/TRIF/RIPK/MLKL signaling. |
doi_str_mv | 10.1016/j.envpol.2022.120217 |
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•Developmental Chlorpyrifos exposure increases pro-inflammatory cytokine production in hippocampus.•Chlorpyrifos-induced necroptosis is involved in activation of microglia.•Developmental CPF exposure causes microglia activation in hippocampus by TLR4/TRIF/RIPK/MLKL signaling.</description><identifier>ISSN: 0269-7491</identifier><identifier>EISSN: 1873-6424</identifier><identifier>DOI: 10.1016/j.envpol.2022.120217</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Chlorpyrifos ; Hippocampus ; Microglia ; Necroptosis ; Toll-like receptor 4</subject><ispartof>Environmental pollution (1987), 2022-12, Vol.314, p.120217-120217, Article 120217</ispartof><rights>2022 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c269t-87bc60c37d43bd30d530a61eedf50509b0393f8b65baa9052946c1eff3864a3c3</citedby><cites>FETCH-LOGICAL-c269t-87bc60c37d43bd30d530a61eedf50509b0393f8b65baa9052946c1eff3864a3c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0269749122014312$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids></links><search><creatorcontrib>Tu, Ying</creatorcontrib><creatorcontrib>Yang, Yongyong</creatorcontrib><creatorcontrib>Wang, Yue</creatorcontrib><creatorcontrib>Wu, Nana</creatorcontrib><creatorcontrib>Tao, Junyan</creatorcontrib><creatorcontrib>Yang, Guanghong</creatorcontrib><creatorcontrib>You, Mingdan</creatorcontrib><title>Developmental exposure to chlorpyrifos causes neuroinflammation via necroptosis in mouse hippocampus and human microglial cell line</title><title>Environmental pollution (1987)</title><description>Neurodevelopmental exposure to chlorpyrifos (CPF) could increase risks for neurological disorders, such as autism spectrum disorder, cognitive impairment, or attention deficit hyperactivity disorder. The potential involvement of microglia reactive to inflammatory stimuli in these neurological disorders has been generally reported. However, the concrete effects and potential mechanisms of microglia dysfunction triggered by developmental CPF exposure remain unclear. Therefore, we established mouse and human embryonic microglial cells (HMC3 cell) models of developmental CPF exposure to evaluate the effects of developmental CPF exposure on neuroinflammation and underlying mechanisms. The results showed that developmental exposure to CPF enhanced the expression of Iba1 in hippocampus. CPF treatment increased inflammatory cytokines levels and TSPO expression in hippocampus and HMC3 cells. The levels of necroptosis and necroptosis-related signaling RIPK/MLKL were increased in hippocampus and HMC3 cells following CPF exposure. Furthermore, the expression of TLR4/TRIF signaling was increased in hippocampus and HMC3 cells subjected to CPF exposure. Notably, the increased levels of TLR4/TRIF signaling, RIPK/MLKL signaling, necroptosis and pro-inflammatory cytokines induced by CPF treatment were remarkably inhibited by TAK-242 (a specific TLR4 inhibitor). Additionally, the necroptosis and pro-inflammatory cytokines production induced by CPF treatment were significantly relieved by Nec-1 (a specific RIPK1 inhibitor). In general, the above results suggested that activated microglia in hippocampus subjected to developmental CPF exposure underwent RIPK1/MLKL-mediated necroptosis regulated by TLR4/TRIF signaling.
[Display omitted]
•Developmental Chlorpyrifos exposure increases pro-inflammatory cytokine production in hippocampus.•Chlorpyrifos-induced necroptosis is involved in activation of microglia.•Developmental CPF exposure causes microglia activation in hippocampus by TLR4/TRIF/RIPK/MLKL signaling.</description><subject>Chlorpyrifos</subject><subject>Hippocampus</subject><subject>Microglia</subject><subject>Necroptosis</subject><subject>Toll-like receptor 4</subject><issn>0269-7491</issn><issn>1873-6424</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9UD1PwzAQtRBIlMI_YPDIkmLHiZMsSKh8SpVYYLYc50JdObaxk4rO_HFchZnlTrp77927h9A1JStKKL_drcDuvTOrnOT5iqZKqxO0oHXFMl7kxSlakJw3WVU09BxdxLgjhBSMsQX6eYA9GOcHsKM0GL69i1MAPDqstsYFfwi6dxErOUWI2MIUnLa9kcMgR-0s3muZpio4P7qoI9YWDy5h8VZ775Qc_BSxtB3eToNMO52gn0anWwqMwUZbuERnvTQRrv76En08Pb6vX7LN2_Pr-n6TqWR-zOqqVZwoVnUFaztGupIRySlA15ekJE1LWMP6uuVlK2VDyrwpuKLQ96zmhWSKLdHNrOuD-5ogjmLQ8ehCWkiWRV7RmjPOCU_QYoYmtzEG6IUPepDhICgRx8zFTsyZi2PmYs480e5mGqQ39hqCiEqDVdDpAGoUndP_C_wCEsaQgA</recordid><startdate>20221201</startdate><enddate>20221201</enddate><creator>Tu, Ying</creator><creator>Yang, Yongyong</creator><creator>Wang, Yue</creator><creator>Wu, Nana</creator><creator>Tao, Junyan</creator><creator>Yang, Guanghong</creator><creator>You, Mingdan</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20221201</creationdate><title>Developmental exposure to chlorpyrifos causes neuroinflammation via necroptosis in mouse hippocampus and human microglial cell line</title><author>Tu, Ying ; Yang, Yongyong ; Wang, Yue ; Wu, Nana ; Tao, Junyan ; Yang, Guanghong ; You, Mingdan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c269t-87bc60c37d43bd30d530a61eedf50509b0393f8b65baa9052946c1eff3864a3c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Chlorpyrifos</topic><topic>Hippocampus</topic><topic>Microglia</topic><topic>Necroptosis</topic><topic>Toll-like receptor 4</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tu, Ying</creatorcontrib><creatorcontrib>Yang, Yongyong</creatorcontrib><creatorcontrib>Wang, Yue</creatorcontrib><creatorcontrib>Wu, Nana</creatorcontrib><creatorcontrib>Tao, Junyan</creatorcontrib><creatorcontrib>Yang, Guanghong</creatorcontrib><creatorcontrib>You, Mingdan</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Environmental pollution (1987)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tu, Ying</au><au>Yang, Yongyong</au><au>Wang, Yue</au><au>Wu, Nana</au><au>Tao, Junyan</au><au>Yang, Guanghong</au><au>You, Mingdan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Developmental exposure to chlorpyrifos causes neuroinflammation via necroptosis in mouse hippocampus and human microglial cell line</atitle><jtitle>Environmental pollution (1987)</jtitle><date>2022-12-01</date><risdate>2022</risdate><volume>314</volume><spage>120217</spage><epage>120217</epage><pages>120217-120217</pages><artnum>120217</artnum><issn>0269-7491</issn><eissn>1873-6424</eissn><abstract>Neurodevelopmental exposure to chlorpyrifos (CPF) could increase risks for neurological disorders, such as autism spectrum disorder, cognitive impairment, or attention deficit hyperactivity disorder. The potential involvement of microglia reactive to inflammatory stimuli in these neurological disorders has been generally reported. However, the concrete effects and potential mechanisms of microglia dysfunction triggered by developmental CPF exposure remain unclear. Therefore, we established mouse and human embryonic microglial cells (HMC3 cell) models of developmental CPF exposure to evaluate the effects of developmental CPF exposure on neuroinflammation and underlying mechanisms. The results showed that developmental exposure to CPF enhanced the expression of Iba1 in hippocampus. CPF treatment increased inflammatory cytokines levels and TSPO expression in hippocampus and HMC3 cells. The levels of necroptosis and necroptosis-related signaling RIPK/MLKL were increased in hippocampus and HMC3 cells following CPF exposure. Furthermore, the expression of TLR4/TRIF signaling was increased in hippocampus and HMC3 cells subjected to CPF exposure. Notably, the increased levels of TLR4/TRIF signaling, RIPK/MLKL signaling, necroptosis and pro-inflammatory cytokines induced by CPF treatment were remarkably inhibited by TAK-242 (a specific TLR4 inhibitor). Additionally, the necroptosis and pro-inflammatory cytokines production induced by CPF treatment were significantly relieved by Nec-1 (a specific RIPK1 inhibitor). In general, the above results suggested that activated microglia in hippocampus subjected to developmental CPF exposure underwent RIPK1/MLKL-mediated necroptosis regulated by TLR4/TRIF signaling.
[Display omitted]
•Developmental Chlorpyrifos exposure increases pro-inflammatory cytokine production in hippocampus.•Chlorpyrifos-induced necroptosis is involved in activation of microglia.•Developmental CPF exposure causes microglia activation in hippocampus by TLR4/TRIF/RIPK/MLKL signaling.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.envpol.2022.120217</doi><tpages>1</tpages></addata></record> |
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subjects | Chlorpyrifos Hippocampus Microglia Necroptosis Toll-like receptor 4 |
title | Developmental exposure to chlorpyrifos causes neuroinflammation via necroptosis in mouse hippocampus and human microglial cell line |
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