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Inhibition of NADPH oxidase blocks NETosis and reduces thrombosis in heparin-induced thrombocytopenia
Heparin-induced thrombocytopenia (HIT) is associated with severe and potentially lethal thrombotic complications. NETosis was recently shown to be an important driver of thrombosis in HIT. We investigated the role of reactive oxygen species (ROS) and nicotinamide adenine dinucleotide phosphate (NADP...
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Published in: | Blood advances 2021-12, Vol.5 (23), p.5439-5451 |
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description | Heparin-induced thrombocytopenia (HIT) is associated with severe and potentially lethal thrombotic complications. NETosis was recently shown to be an important driver of thrombosis in HIT. We investigated the role of reactive oxygen species (ROS) and nicotinamide adenine dinucleotide phosphate (NADPH) oxidase 2 (NOX2) and their contributions to thrombus development in HIT. We showed that neutrophil activation by HIT immune complexes induced ROS-dependent NETosis. Analysis of thrombi formed in a microfluidics system showed ROS production in both platelets and neutrophils, and abundant neutrophil extracellular traps (NETs) and ROS distributed throughout the clot. Neutrophil-targeted ROS inhibition was sufficient to block HIT-induced NETosis and thrombosis using human blood. Inhibition of NOX2 with diphenyleneiodonium chloride or GSK2795039 abrogated HIT-induced thrombi in vivo using FcγRIIa+/hPF4+-transgenic mice. Thrombocytopenia in mice remained unaffected by ROS inhibition. Increased ROS production in activated neutrophils was also confirmed using fresh blood from patients with active HIT. Our findings show that ROS and NOX2 play a crucial role in NETosis and thrombosis in HIT. This enhances our understanding of the processes driving thrombosis in HIT and identifies NOX2 as a potential new therapeutic target for antithrombotic treatment of HIT.
•ROS generation is essential for thrombus formation in HIT.•NOX2 inhibition prevents thrombus formation in a murine model of HIT.
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•ROS generation is essential for thrombus formation in HIT.•NOX2 inhibition prevents thrombus formation in a murine model of HIT.
[Display omitted]</description><identifier>ISSN: 2473-9529</identifier><identifier>ISSN: 2473-9537</identifier><identifier>EISSN: 2473-9537</identifier><identifier>DOI: 10.1182/bloodadvances.2020003093</identifier><identifier>PMID: 34478504</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Extracellular Traps ; Humans ; Mice ; NADPH Oxidases - genetics ; Neutrophil Activation ; Thrombocytopenia - chemically induced ; Thrombosis - chemically induced ; Thrombosis - drug therapy ; Thrombosis and Hemostasis</subject><ispartof>Blood advances, 2021-12, Vol.5 (23), p.5439-5451</ispartof><rights>2021 The American Society of Hematology</rights><rights>2021 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.</rights><rights>2021 by The American Society of Hematology. Licensed under , permitting only noncommercial, nonderivative use with attribution. All other rights reserved. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c479t-22e0b545107db96ceccfa659f48d1269b37832c44a5288f7ebeb7e56bd00e3343</citedby><cites>FETCH-LOGICAL-c479t-22e0b545107db96ceccfa659f48d1269b37832c44a5288f7ebeb7e56bd00e3343</cites><orcidid>0000-0003-4959-3209 ; 0000-0002-1554-708X ; 0000-0002-7561-490X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9153028/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S2473952921005048$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,3549,27924,27925,45780,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34478504$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Leung, Halina H.L.</creatorcontrib><creatorcontrib>Perdomo, Jose</creatorcontrib><creatorcontrib>Ahmadi, Zohra</creatorcontrib><creatorcontrib>Yan, Feng</creatorcontrib><creatorcontrib>McKenzie, Steven E.</creatorcontrib><creatorcontrib>Chong, Beng H.</creatorcontrib><title>Inhibition of NADPH oxidase blocks NETosis and reduces thrombosis in heparin-induced thrombocytopenia</title><title>Blood advances</title><addtitle>Blood Adv</addtitle><description>Heparin-induced thrombocytopenia (HIT) is associated with severe and potentially lethal thrombotic complications. NETosis was recently shown to be an important driver of thrombosis in HIT. We investigated the role of reactive oxygen species (ROS) and nicotinamide adenine dinucleotide phosphate (NADPH) oxidase 2 (NOX2) and their contributions to thrombus development in HIT. We showed that neutrophil activation by HIT immune complexes induced ROS-dependent NETosis. Analysis of thrombi formed in a microfluidics system showed ROS production in both platelets and neutrophils, and abundant neutrophil extracellular traps (NETs) and ROS distributed throughout the clot. Neutrophil-targeted ROS inhibition was sufficient to block HIT-induced NETosis and thrombosis using human blood. Inhibition of NOX2 with diphenyleneiodonium chloride or GSK2795039 abrogated HIT-induced thrombi in vivo using FcγRIIa+/hPF4+-transgenic mice. Thrombocytopenia in mice remained unaffected by ROS inhibition. Increased ROS production in activated neutrophils was also confirmed using fresh blood from patients with active HIT. Our findings show that ROS and NOX2 play a crucial role in NETosis and thrombosis in HIT. This enhances our understanding of the processes driving thrombosis in HIT and identifies NOX2 as a potential new therapeutic target for antithrombotic treatment of HIT.
•ROS generation is essential for thrombus formation in HIT.•NOX2 inhibition prevents thrombus formation in a murine model of HIT.
[Display omitted]</description><subject>Animals</subject><subject>Extracellular Traps</subject><subject>Humans</subject><subject>Mice</subject><subject>NADPH Oxidases - genetics</subject><subject>Neutrophil Activation</subject><subject>Thrombocytopenia - chemically induced</subject><subject>Thrombosis - chemically induced</subject><subject>Thrombosis - drug therapy</subject><subject>Thrombosis and Hemostasis</subject><issn>2473-9529</issn><issn>2473-9537</issn><issn>2473-9537</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkU1PVDEYhRsjEYL8BdKlm4u9_bhtNyaICCQEWcC66cd7neqddmzvTOTfWxgYZeWqTc_znvOmByHck5O-V_Sjm3IONmxs8lBPKKGEEEY0e4MOKJes04LJt7s71fvoqNYfDerlwISm79A-41wqQfgBgqu0iC7OMSecR3xz-uX2EuffMdgKuCX5nxXfnN_lGiu2KeACYd1i8bwoeemenmPCC1jZElMX06MaXlT_MOcVpGjfo73RThWOns9DdP_1_O7ssrv-dnF1dnrdeS713FEKxAkueiKD04MH70c7CD1yFXo6aMekYtRzbgVVapTgwEkQgwuEAGOcHaJPW9_V2i0heEhzsZNZlbi05cFkG81rJcWF-Z43RveCEaqawYdng5J_raHOZhmrh2myCfK6GioGzVQjRUPVFvUl11pg3MX0xDwWZV4VZf4W1UaP_11zN_hSSwM-bwFon7WJUEz1EZpNiAX8bEKO_0_5AzEfrDw</recordid><startdate>20211214</startdate><enddate>20211214</enddate><creator>Leung, Halina H.L.</creator><creator>Perdomo, Jose</creator><creator>Ahmadi, Zohra</creator><creator>Yan, Feng</creator><creator>McKenzie, Steven E.</creator><creator>Chong, Beng H.</creator><general>Elsevier Inc</general><general>American Society of Hematology</general><scope>6I.</scope><scope>AAFTH</scope><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>5PM</scope><orcidid>https://orcid.org/0000-0003-4959-3209</orcidid><orcidid>https://orcid.org/0000-0002-1554-708X</orcidid><orcidid>https://orcid.org/0000-0002-7561-490X</orcidid></search><sort><creationdate>20211214</creationdate><title>Inhibition of NADPH oxidase blocks NETosis and reduces thrombosis in heparin-induced thrombocytopenia</title><author>Leung, Halina H.L. ; Perdomo, Jose ; Ahmadi, Zohra ; Yan, Feng ; McKenzie, Steven E. ; Chong, Beng H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c479t-22e0b545107db96ceccfa659f48d1269b37832c44a5288f7ebeb7e56bd00e3343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Extracellular Traps</topic><topic>Humans</topic><topic>Mice</topic><topic>NADPH Oxidases - genetics</topic><topic>Neutrophil Activation</topic><topic>Thrombocytopenia - chemically induced</topic><topic>Thrombosis - chemically induced</topic><topic>Thrombosis - drug therapy</topic><topic>Thrombosis and Hemostasis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Leung, Halina H.L.</creatorcontrib><creatorcontrib>Perdomo, Jose</creatorcontrib><creatorcontrib>Ahmadi, Zohra</creatorcontrib><creatorcontrib>Yan, Feng</creatorcontrib><creatorcontrib>McKenzie, Steven E.</creatorcontrib><creatorcontrib>Chong, Beng H.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Blood advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Leung, Halina H.L.</au><au>Perdomo, Jose</au><au>Ahmadi, Zohra</au><au>Yan, Feng</au><au>McKenzie, Steven E.</au><au>Chong, Beng H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibition of NADPH oxidase blocks NETosis and reduces thrombosis in heparin-induced thrombocytopenia</atitle><jtitle>Blood advances</jtitle><addtitle>Blood Adv</addtitle><date>2021-12-14</date><risdate>2021</risdate><volume>5</volume><issue>23</issue><spage>5439</spage><epage>5451</epage><pages>5439-5451</pages><issn>2473-9529</issn><issn>2473-9537</issn><eissn>2473-9537</eissn><abstract>Heparin-induced thrombocytopenia (HIT) is associated with severe and potentially lethal thrombotic complications. NETosis was recently shown to be an important driver of thrombosis in HIT. We investigated the role of reactive oxygen species (ROS) and nicotinamide adenine dinucleotide phosphate (NADPH) oxidase 2 (NOX2) and their contributions to thrombus development in HIT. We showed that neutrophil activation by HIT immune complexes induced ROS-dependent NETosis. Analysis of thrombi formed in a microfluidics system showed ROS production in both platelets and neutrophils, and abundant neutrophil extracellular traps (NETs) and ROS distributed throughout the clot. Neutrophil-targeted ROS inhibition was sufficient to block HIT-induced NETosis and thrombosis using human blood. Inhibition of NOX2 with diphenyleneiodonium chloride or GSK2795039 abrogated HIT-induced thrombi in vivo using FcγRIIa+/hPF4+-transgenic mice. Thrombocytopenia in mice remained unaffected by ROS inhibition. Increased ROS production in activated neutrophils was also confirmed using fresh blood from patients with active HIT. Our findings show that ROS and NOX2 play a crucial role in NETosis and thrombosis in HIT. This enhances our understanding of the processes driving thrombosis in HIT and identifies NOX2 as a potential new therapeutic target for antithrombotic treatment of HIT.
•ROS generation is essential for thrombus formation in HIT.•NOX2 inhibition prevents thrombus formation in a murine model of HIT.
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subjects | Animals Extracellular Traps Humans Mice NADPH Oxidases - genetics Neutrophil Activation Thrombocytopenia - chemically induced Thrombosis - chemically induced Thrombosis - drug therapy Thrombosis and Hemostasis |
title | Inhibition of NADPH oxidase blocks NETosis and reduces thrombosis in heparin-induced thrombocytopenia |
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