Photophosphatidylserine Guides Natural Killer Cell Photoimmunotherapy via Tim‑3
Natural killer (NK) cells, in addition to their cytotoxicity function, harbor prominent cytokine production capabilities and contribute to regulating autoimmune responses. T-cell immunoglobulin and mucin domain containing protein-3 (Tim-3) is one of the inhibitory receptors on NK cells and a promisi...
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Veröffentlicht in: | Journal of the American Chemical Society 2022-03, Vol.144 (9), p.3863-3874 |
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creator | Yang, Xingye Li, Mengzhen Qin, Xiaojun Tan, Siyu Du, Lupei Ma, Chunhong Li, Minyong |
description | Natural killer (NK) cells, in addition to their cytotoxicity function, harbor prominent cytokine production capabilities and contribute to regulating autoimmune responses. T-cell immunoglobulin and mucin domain containing protein-3 (Tim-3) is one of the inhibitory receptors on NK cells and a promising immune checkpoint target. We recently found that phosphatidylserine (PS) binding to Tim-3 can suppress NK cell activation. Therefore, based on the therapeutic potential of Tim-3 in NK-cell-mediated diseases, we developed a photoswitchable ligand of Tim-3, termed photophosphatidylserine (phoPS), that mimics the effects of PS. Upon 365 or 455 nm light irradiation, the isomer of phoPS cyclically conversed the cis/trans configuration, resulting in an active/inactive Tim-3 ligand, thus modulating the function of NK cells in vitro and in vivo. We also demonstrated that reversible phoPS enabled optical control of acute hepatitis. Together, phoPS may be an appealing tool for autoimmune diseases and cytokine storms in the future. |
doi_str_mv | 10.1021/jacs.1c11498 |
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T-cell immunoglobulin and mucin domain containing protein-3 (Tim-3) is one of the inhibitory receptors on NK cells and a promising immune checkpoint target. We recently found that phosphatidylserine (PS) binding to Tim-3 can suppress NK cell activation. Therefore, based on the therapeutic potential of Tim-3 in NK-cell-mediated diseases, we developed a photoswitchable ligand of Tim-3, termed photophosphatidylserine (phoPS), that mimics the effects of PS. Upon 365 or 455 nm light irradiation, the isomer of phoPS cyclically conversed the cis/trans configuration, resulting in an active/inactive Tim-3 ligand, thus modulating the function of NK cells in vitro and in vivo. We also demonstrated that reversible phoPS enabled optical control of acute hepatitis. Together, phoPS may be an appealing tool for autoimmune diseases and cytokine storms in the future.</description><identifier>ISSN: 0002-7863</identifier><identifier>EISSN: 1520-5126</identifier><identifier>DOI: 10.1021/jacs.1c11498</identifier><identifier>PMID: 35226805</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Hepatitis A Virus Cellular Receptor 2 - metabolism ; Immunotherapy ; Killer Cells, Natural - metabolism ; Ligands ; Lymphocyte Activation</subject><ispartof>Journal of the American Chemical Society, 2022-03, Vol.144 (9), p.3863-3874</ispartof><rights>2022 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a324t-1e275df9add926bbcdd8d13f57978d5e3155c75749439b11fe8300341aebfd8c3</citedby><cites>FETCH-LOGICAL-a324t-1e275df9add926bbcdd8d13f57978d5e3155c75749439b11fe8300341aebfd8c3</cites><orcidid>0000-0003-3276-4921 ; 0000-0003-0531-8985</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jacs.1c11498$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jacs.1c11498$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35226805$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Xingye</creatorcontrib><creatorcontrib>Li, Mengzhen</creatorcontrib><creatorcontrib>Qin, Xiaojun</creatorcontrib><creatorcontrib>Tan, Siyu</creatorcontrib><creatorcontrib>Du, Lupei</creatorcontrib><creatorcontrib>Ma, Chunhong</creatorcontrib><creatorcontrib>Li, Minyong</creatorcontrib><title>Photophosphatidylserine Guides Natural Killer Cell Photoimmunotherapy via Tim‑3</title><title>Journal of the American Chemical Society</title><addtitle>J. Am. Chem. Soc</addtitle><description>Natural killer (NK) cells, in addition to their cytotoxicity function, harbor prominent cytokine production capabilities and contribute to regulating autoimmune responses. T-cell immunoglobulin and mucin domain containing protein-3 (Tim-3) is one of the inhibitory receptors on NK cells and a promising immune checkpoint target. We recently found that phosphatidylserine (PS) binding to Tim-3 can suppress NK cell activation. Therefore, based on the therapeutic potential of Tim-3 in NK-cell-mediated diseases, we developed a photoswitchable ligand of Tim-3, termed photophosphatidylserine (phoPS), that mimics the effects of PS. Upon 365 or 455 nm light irradiation, the isomer of phoPS cyclically conversed the cis/trans configuration, resulting in an active/inactive Tim-3 ligand, thus modulating the function of NK cells in vitro and in vivo. We also demonstrated that reversible phoPS enabled optical control of acute hepatitis. Together, phoPS may be an appealing tool for autoimmune diseases and cytokine storms in the future.</description><subject>Hepatitis A Virus Cellular Receptor 2 - metabolism</subject><subject>Immunotherapy</subject><subject>Killer Cells, Natural - metabolism</subject><subject>Ligands</subject><subject>Lymphocyte Activation</subject><issn>0002-7863</issn><issn>1520-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkM1KxDAUhYMoTh3duZYsXdgxN2nadCmDjuLgD4zrkjYpzdA_klbozlfwFX0SW2d05epy4DuHy4fQOZAFEArXW5m5BWQAQSwOkAecEp8DDQ-RRwihfiRCNkMnzm3HGFABx2jGOKWhINxDry9F0zVt0bi2kJ1RQ-m0NbXGq94o7fCT7HorS_xoylJbvNRliX8qpqr6uukKbWU74Hcj8cZUXx-f7BQd5XJcOdvfOXq7u90s7_318-phebP2JaNB54OmEVd5LJWKaZimmVJCAct5FEdCcc2A8yziURAHLE4Bci0YISwAqdNciYzN0dVuN7ONc1bnSWtNJe2QAEkmM8lkJtmbGfGLHd72aaXVH_yrYgQud8DU2ja9rcfv_9_6BqRNboE</recordid><startdate>20220309</startdate><enddate>20220309</enddate><creator>Yang, Xingye</creator><creator>Li, Mengzhen</creator><creator>Qin, Xiaojun</creator><creator>Tan, Siyu</creator><creator>Du, Lupei</creator><creator>Ma, Chunhong</creator><creator>Li, Minyong</creator><general>American Chemical Society</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><orcidid>https://orcid.org/0000-0003-3276-4921</orcidid><orcidid>https://orcid.org/0000-0003-0531-8985</orcidid></search><sort><creationdate>20220309</creationdate><title>Photophosphatidylserine Guides Natural Killer Cell Photoimmunotherapy via Tim‑3</title><author>Yang, Xingye ; Li, Mengzhen ; Qin, Xiaojun ; Tan, Siyu ; Du, Lupei ; Ma, Chunhong ; Li, Minyong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a324t-1e275df9add926bbcdd8d13f57978d5e3155c75749439b11fe8300341aebfd8c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Hepatitis A Virus Cellular Receptor 2 - metabolism</topic><topic>Immunotherapy</topic><topic>Killer Cells, Natural - metabolism</topic><topic>Ligands</topic><topic>Lymphocyte Activation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Xingye</creatorcontrib><creatorcontrib>Li, Mengzhen</creatorcontrib><creatorcontrib>Qin, Xiaojun</creatorcontrib><creatorcontrib>Tan, Siyu</creatorcontrib><creatorcontrib>Du, Lupei</creatorcontrib><creatorcontrib>Ma, Chunhong</creatorcontrib><creatorcontrib>Li, Minyong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of the American Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Xingye</au><au>Li, Mengzhen</au><au>Qin, Xiaojun</au><au>Tan, Siyu</au><au>Du, Lupei</au><au>Ma, Chunhong</au><au>Li, Minyong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photophosphatidylserine Guides Natural Killer Cell Photoimmunotherapy via Tim‑3</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J. Am. Chem. Soc</addtitle><date>2022-03-09</date><risdate>2022</risdate><volume>144</volume><issue>9</issue><spage>3863</spage><epage>3874</epage><pages>3863-3874</pages><issn>0002-7863</issn><eissn>1520-5126</eissn><abstract>Natural killer (NK) cells, in addition to their cytotoxicity function, harbor prominent cytokine production capabilities and contribute to regulating autoimmune responses. T-cell immunoglobulin and mucin domain containing protein-3 (Tim-3) is one of the inhibitory receptors on NK cells and a promising immune checkpoint target. We recently found that phosphatidylserine (PS) binding to Tim-3 can suppress NK cell activation. Therefore, based on the therapeutic potential of Tim-3 in NK-cell-mediated diseases, we developed a photoswitchable ligand of Tim-3, termed photophosphatidylserine (phoPS), that mimics the effects of PS. Upon 365 or 455 nm light irradiation, the isomer of phoPS cyclically conversed the cis/trans configuration, resulting in an active/inactive Tim-3 ligand, thus modulating the function of NK cells in vitro and in vivo. We also demonstrated that reversible phoPS enabled optical control of acute hepatitis. Together, phoPS may be an appealing tool for autoimmune diseases and cytokine storms in the future.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>35226805</pmid><doi>10.1021/jacs.1c11498</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-3276-4921</orcidid><orcidid>https://orcid.org/0000-0003-0531-8985</orcidid></addata></record> |
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subjects | Hepatitis A Virus Cellular Receptor 2 - metabolism Immunotherapy Killer Cells, Natural - metabolism Ligands Lymphocyte Activation |
title | Photophosphatidylserine Guides Natural Killer Cell Photoimmunotherapy via Tim‑3 |
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