Downregulation of miR-199b promotes the acute spinal cord injury through IKKβ-NF-κB signaling pathway activating microglial cells

Inflammatory response played an important role in the progression of spinal cord injury (SCI). Several miRNAs were associated with the pathology of SCI. However, the molecular mechanism of miRNA involving in inflammatory response in acute SCI (ASCI) was poorly understood. Sprague-Dawley (SD) rats we...

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Veröffentlicht in:Experimental cell research 2016-11, Vol.349 (1), p.60-67
Hauptverfasser: Zhou, Heng-Jun, Wang, Li-Qing, Xu, Qing-Sheng, Fan, Zuo-Xu, Zhu, Yu, Jiang, Hao, Zheng, Xiu-Jue, Ma, Yue-Hui, Zhan, Ren-Ya
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container_issue 1
container_start_page 60
container_title Experimental cell research
container_volume 349
creator Zhou, Heng-Jun
Wang, Li-Qing
Xu, Qing-Sheng
Fan, Zuo-Xu
Zhu, Yu
Jiang, Hao
Zheng, Xiu-Jue
Ma, Yue-Hui
Zhan, Ren-Ya
description Inflammatory response played an important role in the progression of spinal cord injury (SCI). Several miRNAs were associated with the pathology of SCI. However, the molecular mechanism of miRNA involving in inflammatory response in acute SCI (ASCI) was poorly understood. Sprague-Dawley (SD) rats were divided into 2 groups: control group (n=6) and acute SCI (ASCI) group (n=6). The expression of miR-199b and IκB kinase β-nuclear factor-kappa B (IKKβ-NF-κB) signaling pathway were evaluated by quantitative reverse transcription-PCR (qRT-PCR) in rats with ASCI and in primary microglia activated by lipopolysaccharide (LPS). We found that downregulation of miR-199b and activation of IKKβ/NF-κB were observed in rats after ASCI and in activated microglia. miR-199b negatively regulated IKKβ by targeting its 3′- untranslated regions (UTR) through using luciferase reporter assay. Overexpression of miR-199b reversed the up-regulation of IKKβ, p-p65, tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) in LPS-treated BV2 cells assessed by western blotting analysis. In addition, BMS-345541 reversed the up-regulation effects of miR-199b inhibitor on the expression of TNF-α and IL-1β. In the SCI rats, overexpression of miR-199b attenuated ASCI and decreased the expression of IKKβ-NF-κB signaling pathway and TNF-α and IL-1β. These results indicated that miR-199b attenuated ASCI at least partly through IKKβ-NF-κB signaling pathway and affecting the function of microglia. Our findings suggest that miR-199b may be employed as therapeutic for spinal cord injury. •Downregulation of miR-199b and activation of IKKβ/NF-κB were observed in rat after SCI.•miR-199b negatively regulated IKKβ by targeting its 3′-UTR.•miR-199b overexpression reversed the increasing IKKβ, p-p65, TNF-α and IL-1β in LPS-treated BV2.•BMS-345541 reversed the up-regulation of TNF-α and IL-1β induced by miR-199b inhibitor.•Overexpression of miR-199b attenuated ASCI and decreased the expression of IKKβ-NF-κB in rats.
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Several miRNAs were associated with the pathology of SCI. However, the molecular mechanism of miRNA involving in inflammatory response in acute SCI (ASCI) was poorly understood. Sprague-Dawley (SD) rats were divided into 2 groups: control group (n=6) and acute SCI (ASCI) group (n=6). The expression of miR-199b and IκB kinase β-nuclear factor-kappa B (IKKβ-NF-κB) signaling pathway were evaluated by quantitative reverse transcription-PCR (qRT-PCR) in rats with ASCI and in primary microglia activated by lipopolysaccharide (LPS). We found that downregulation of miR-199b and activation of IKKβ/NF-κB were observed in rats after ASCI and in activated microglia. miR-199b negatively regulated IKKβ by targeting its 3′- untranslated regions (UTR) through using luciferase reporter assay. Overexpression of miR-199b reversed the up-regulation of IKKβ, p-p65, tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) in LPS-treated BV2 cells assessed by western blotting analysis. In addition, BMS-345541 reversed the up-regulation effects of miR-199b inhibitor on the expression of TNF-α and IL-1β. In the SCI rats, overexpression of miR-199b attenuated ASCI and decreased the expression of IKKβ-NF-κB signaling pathway and TNF-α and IL-1β. These results indicated that miR-199b attenuated ASCI at least partly through IKKβ-NF-κB signaling pathway and affecting the function of microglia. Our findings suggest that miR-199b may be employed as therapeutic for spinal cord injury. •Downregulation of miR-199b and activation of IKKβ/NF-κB were observed in rat after SCI.•miR-199b negatively regulated IKKβ by targeting its 3′-UTR.•miR-199b overexpression reversed the increasing IKKβ, p-p65, TNF-α and IL-1β in LPS-treated BV2.•BMS-345541 reversed the up-regulation of TNF-α and IL-1β induced by miR-199b inhibitor.•Overexpression of miR-199b attenuated ASCI and decreased the expression of IKKβ-NF-κB in rats.</description><identifier>ISSN: 0014-4827</identifier><identifier>EISSN: 1090-2422</identifier><identifier>DOI: 10.1016/j.yexcr.2016.09.020</identifier><identifier>PMID: 27693495</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>60 APPLIED LIFE SCIENCES ; Acute Disease ; Animals ; Down-Regulation ; Female ; I-kappa B Kinase - metabolism ; IKKβ-NF-κB signaling pathway ; INFLAMMATION ; Inflammation - pathology ; INJURIES ; LIPOPOLYSACCHARIDES ; LUCIFERASE ; LYMPHOKINES ; Mice ; Microglia ; Microglia - metabolism ; Microglia - pathology ; MicroRNAs - genetics ; MicroRNAs - metabolism ; MiR-199b ; NECROSIS ; NEOPLASMS ; NF-kappa B - metabolism ; PATHOLOGY ; PHOSPHOTRANSFERASES ; POLYMERASE CHAIN REACTION ; RATS ; Rats, Sprague-Dawley ; Signal Transduction ; SPINAL CORD ; Spinal Cord Injuries - genetics ; Spinal Cord Injuries - pathology ; Spinal cord injury ; TRANSCRIPTION ; Transcription Factor RelA - metabolism ; Up-Regulation - genetics</subject><ispartof>Experimental cell research, 2016-11, Vol.349 (1), p.60-67</ispartof><rights>2016 Elsevier Inc.</rights><rights>Copyright © 2016 Elsevier Inc. 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Several miRNAs were associated with the pathology of SCI. However, the molecular mechanism of miRNA involving in inflammatory response in acute SCI (ASCI) was poorly understood. Sprague-Dawley (SD) rats were divided into 2 groups: control group (n=6) and acute SCI (ASCI) group (n=6). The expression of miR-199b and IκB kinase β-nuclear factor-kappa B (IKKβ-NF-κB) signaling pathway were evaluated by quantitative reverse transcription-PCR (qRT-PCR) in rats with ASCI and in primary microglia activated by lipopolysaccharide (LPS). We found that downregulation of miR-199b and activation of IKKβ/NF-κB were observed in rats after ASCI and in activated microglia. miR-199b negatively regulated IKKβ by targeting its 3′- untranslated regions (UTR) through using luciferase reporter assay. Overexpression of miR-199b reversed the up-regulation of IKKβ, p-p65, tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) in LPS-treated BV2 cells assessed by western blotting analysis. In addition, BMS-345541 reversed the up-regulation effects of miR-199b inhibitor on the expression of TNF-α and IL-1β. In the SCI rats, overexpression of miR-199b attenuated ASCI and decreased the expression of IKKβ-NF-κB signaling pathway and TNF-α and IL-1β. These results indicated that miR-199b attenuated ASCI at least partly through IKKβ-NF-κB signaling pathway and affecting the function of microglia. Our findings suggest that miR-199b may be employed as therapeutic for spinal cord injury. •Downregulation of miR-199b and activation of IKKβ/NF-κB were observed in rat after SCI.•miR-199b negatively regulated IKKβ by targeting its 3′-UTR.•miR-199b overexpression reversed the increasing IKKβ, p-p65, TNF-α and IL-1β in LPS-treated BV2.•BMS-345541 reversed the up-regulation of TNF-α and IL-1β induced by miR-199b inhibitor.•Overexpression of miR-199b attenuated ASCI and decreased the expression of IKKβ-NF-κB in rats.</description><subject>60 APPLIED LIFE SCIENCES</subject><subject>Acute Disease</subject><subject>Animals</subject><subject>Down-Regulation</subject><subject>Female</subject><subject>I-kappa B Kinase - metabolism</subject><subject>IKKβ-NF-κB signaling pathway</subject><subject>INFLAMMATION</subject><subject>Inflammation - pathology</subject><subject>INJURIES</subject><subject>LIPOPOLYSACCHARIDES</subject><subject>LUCIFERASE</subject><subject>LYMPHOKINES</subject><subject>Mice</subject><subject>Microglia</subject><subject>Microglia - metabolism</subject><subject>Microglia - pathology</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>MiR-199b</subject><subject>NECROSIS</subject><subject>NEOPLASMS</subject><subject>NF-kappa B - metabolism</subject><subject>PATHOLOGY</subject><subject>PHOSPHOTRANSFERASES</subject><subject>POLYMERASE CHAIN REACTION</subject><subject>RATS</subject><subject>Rats, Sprague-Dawley</subject><subject>Signal Transduction</subject><subject>SPINAL CORD</subject><subject>Spinal Cord Injuries - genetics</subject><subject>Spinal Cord Injuries - pathology</subject><subject>Spinal cord injury</subject><subject>TRANSCRIPTION</subject><subject>Transcription Factor RelA - metabolism</subject><subject>Up-Regulation - genetics</subject><issn>0014-4827</issn><issn>1090-2422</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1uFDEQhS0EIpOBEyAhS2zYdOOf_vOCBYQEokQgIVhbHru6x6Nue7DdCbPmRiw5RM6EmwksWVl2fe9VlR9CzygpKaHNq115gO86lCxfSiJKwsgDtKJEkIJVjD1EK0JoVVQda0_QaYw7QkjX0eYxOmFtI3gl6hX68c7fugDDPKpkvcO-x5P9XFAhNngf_OQTRJy2gJWeE-C4t06NWPtgsHW7ORxyMfh52OLLq6u7n8XHi-Lu11sc7ZA56wa8V2l7qw5Zn-xN7pGfJquDH0a7GME4xifoUa_GCE_vzzX6enH-5exDcf3p_eXZm-tC865NRd9ueuhBdEY1RtNeUKpa0ggQVDWsga7inJqqooR3RNR9LzTjdWZNrZQyG75GL46-PiYro7YJ9FZ750AnyVhTiTZ7rNHLI5XX_zZDTHKycZlTOfBzlLTjNa-6uiEZ5Uc07xNjgF7ug51UOEhK5JKR3Mk_GcklI0mEzBll1fP7BvNmAvNP8zeUDLw-ApA_48ZCWGYFp8HYsIxqvP1vg98e-aaw</recordid><startdate>20161115</startdate><enddate>20161115</enddate><creator>Zhou, Heng-Jun</creator><creator>Wang, Li-Qing</creator><creator>Xu, Qing-Sheng</creator><creator>Fan, Zuo-Xu</creator><creator>Zhu, Yu</creator><creator>Jiang, Hao</creator><creator>Zheng, Xiu-Jue</creator><creator>Ma, Yue-Hui</creator><creator>Zhan, Ren-Ya</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><scope>OTOTI</scope></search><sort><creationdate>20161115</creationdate><title>Downregulation of miR-199b promotes the acute spinal cord injury through IKKβ-NF-κB signaling pathway activating microglial cells</title><author>Zhou, Heng-Jun ; 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Several miRNAs were associated with the pathology of SCI. However, the molecular mechanism of miRNA involving in inflammatory response in acute SCI (ASCI) was poorly understood. Sprague-Dawley (SD) rats were divided into 2 groups: control group (n=6) and acute SCI (ASCI) group (n=6). The expression of miR-199b and IκB kinase β-nuclear factor-kappa B (IKKβ-NF-κB) signaling pathway were evaluated by quantitative reverse transcription-PCR (qRT-PCR) in rats with ASCI and in primary microglia activated by lipopolysaccharide (LPS). We found that downregulation of miR-199b and activation of IKKβ/NF-κB were observed in rats after ASCI and in activated microglia. miR-199b negatively regulated IKKβ by targeting its 3′- untranslated regions (UTR) through using luciferase reporter assay. Overexpression of miR-199b reversed the up-regulation of IKKβ, p-p65, tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) in LPS-treated BV2 cells assessed by western blotting analysis. In addition, BMS-345541 reversed the up-regulation effects of miR-199b inhibitor on the expression of TNF-α and IL-1β. In the SCI rats, overexpression of miR-199b attenuated ASCI and decreased the expression of IKKβ-NF-κB signaling pathway and TNF-α and IL-1β. These results indicated that miR-199b attenuated ASCI at least partly through IKKβ-NF-κB signaling pathway and affecting the function of microglia. Our findings suggest that miR-199b may be employed as therapeutic for spinal cord injury. •Downregulation of miR-199b and activation of IKKβ/NF-κB were observed in rat after SCI.•miR-199b negatively regulated IKKβ by targeting its 3′-UTR.•miR-199b overexpression reversed the increasing IKKβ, p-p65, TNF-α and IL-1β in LPS-treated BV2.•BMS-345541 reversed the up-regulation of TNF-α and IL-1β induced by miR-199b inhibitor.•Overexpression of miR-199b attenuated ASCI and decreased the expression of IKKβ-NF-κB in rats.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>27693495</pmid><doi>10.1016/j.yexcr.2016.09.020</doi><tpages>8</tpages></addata></record>
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subjects 60 APPLIED LIFE SCIENCES
Acute Disease
Animals
Down-Regulation
Female
I-kappa B Kinase - metabolism
IKKβ-NF-κB signaling pathway
INFLAMMATION
Inflammation - pathology
INJURIES
LIPOPOLYSACCHARIDES
LUCIFERASE
LYMPHOKINES
Mice
Microglia
Microglia - metabolism
Microglia - pathology
MicroRNAs - genetics
MicroRNAs - metabolism
MiR-199b
NECROSIS
NEOPLASMS
NF-kappa B - metabolism
PATHOLOGY
PHOSPHOTRANSFERASES
POLYMERASE CHAIN REACTION
RATS
Rats, Sprague-Dawley
Signal Transduction
SPINAL CORD
Spinal Cord Injuries - genetics
Spinal Cord Injuries - pathology
Spinal cord injury
TRANSCRIPTION
Transcription Factor RelA - metabolism
Up-Regulation - genetics
title Downregulation of miR-199b promotes the acute spinal cord injury through IKKβ-NF-κB signaling pathway activating microglial cells
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