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Targeted regulation of neuroinflammation via nanobiosignaler for repairing the central nerve system injuries
Neuroinflammation, commonly associated with various central nervous system (CNS) diseases such as postoperative cognitive dysfunction (POCD), is primarily mediated by the disruption of biological signals in microglia. However, the effective treatment of CNS diseases remains an ongoing challenge as b...
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Published in: | Nano research 2023-02, Vol.16 (2), p.2938-2948 |
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container_title | Nano research |
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creator | Sun, Xiaoru Ruan, Huitong Liu, Qidong Cao, Silu Jing, Qi Xu, Yaru Xiong, Lize Cui, Wenguo Li, Cheng |
description | Neuroinflammation, commonly associated with various central nervous system (CNS) diseases such as postoperative cognitive dysfunction (POCD), is primarily mediated by the disruption of biological signals in microglia. However, the effective treatment of CNS diseases remains an ongoing challenge as biological signals show limited microglia-targeting effect. In this study, taking advantage of the highly expressed lipoprotein receptor-related protein-1 (LRP1) on the microglia, a nanobiosignal delivery system modified by LRP1 high-affinity peptide ligand RAP12 (RAP: receptor-associated protein) was constructed to specifically regulate neuroinflammation via targeting microglia. The uptake of the RAP12 modified-nanobiosignaler by microglia increased significantly, indicating its microglia-targeting ability. Both
in vitro/vivo
studies proved that the “nanobiosignaler” significantly reduced the secretion of pro-inflammatory cytokines, induced specific M2 (anti-inflammatory type) microglia differentiation, and remarkably alleviated cognitive function impairment in the mice model when compared with unmodified groups. It was indicated that the “nanobiosignaler” could target microglia to deliver the biological signal and inhibit the excessive activation of microglia. Overall, the cell-targeted biological signal transmission system inspired by “nanobiosignaler” has broad application prospects in the future. |
doi_str_mv | 10.1007/s12274-022-5143-3 |
format | article |
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in vitro/vivo
studies proved that the “nanobiosignaler” significantly reduced the secretion of pro-inflammatory cytokines, induced specific M2 (anti-inflammatory type) microglia differentiation, and remarkably alleviated cognitive function impairment in the mice model when compared with unmodified groups. It was indicated that the “nanobiosignaler” could target microglia to deliver the biological signal and inhibit the excessive activation of microglia. Overall, the cell-targeted biological signal transmission system inspired by “nanobiosignaler” has broad application prospects in the future.</description><identifier>ISSN: 1998-0124</identifier><identifier>EISSN: 1998-0000</identifier><identifier>DOI: 10.1007/s12274-022-5143-3</identifier><language>eng</language><publisher>Beijing: Tsinghua University Press</publisher><subject>Atomic/Molecular Structure and Spectra ; Biomedicine ; Biotechnology ; Chemistry and Materials Science ; Condensed Matter Physics ; Materials Science ; Nanotechnology ; Research Article</subject><ispartof>Nano research, 2023-02, Vol.16 (2), p.2938-2948</ispartof><rights>Tsinghua University Press 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c218t-719b6e7ecb08fa4dff7db846fa830cc90e177acd535927928595e702c3fafc803</citedby><cites>FETCH-LOGICAL-c218t-719b6e7ecb08fa4dff7db846fa830cc90e177acd535927928595e702c3fafc803</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Sun, Xiaoru</creatorcontrib><creatorcontrib>Ruan, Huitong</creatorcontrib><creatorcontrib>Liu, Qidong</creatorcontrib><creatorcontrib>Cao, Silu</creatorcontrib><creatorcontrib>Jing, Qi</creatorcontrib><creatorcontrib>Xu, Yaru</creatorcontrib><creatorcontrib>Xiong, Lize</creatorcontrib><creatorcontrib>Cui, Wenguo</creatorcontrib><creatorcontrib>Li, Cheng</creatorcontrib><title>Targeted regulation of neuroinflammation via nanobiosignaler for repairing the central nerve system injuries</title><title>Nano research</title><addtitle>Nano Res</addtitle><description>Neuroinflammation, commonly associated with various central nervous system (CNS) diseases such as postoperative cognitive dysfunction (POCD), is primarily mediated by the disruption of biological signals in microglia. However, the effective treatment of CNS diseases remains an ongoing challenge as biological signals show limited microglia-targeting effect. In this study, taking advantage of the highly expressed lipoprotein receptor-related protein-1 (LRP1) on the microglia, a nanobiosignal delivery system modified by LRP1 high-affinity peptide ligand RAP12 (RAP: receptor-associated protein) was constructed to specifically regulate neuroinflammation via targeting microglia. The uptake of the RAP12 modified-nanobiosignaler by microglia increased significantly, indicating its microglia-targeting ability. Both
in vitro/vivo
studies proved that the “nanobiosignaler” significantly reduced the secretion of pro-inflammatory cytokines, induced specific M2 (anti-inflammatory type) microglia differentiation, and remarkably alleviated cognitive function impairment in the mice model when compared with unmodified groups. It was indicated that the “nanobiosignaler” could target microglia to deliver the biological signal and inhibit the excessive activation of microglia. Overall, the cell-targeted biological signal transmission system inspired by “nanobiosignaler” has broad application prospects in the future.</description><subject>Atomic/Molecular Structure and Spectra</subject><subject>Biomedicine</subject><subject>Biotechnology</subject><subject>Chemistry and Materials Science</subject><subject>Condensed Matter Physics</subject><subject>Materials Science</subject><subject>Nanotechnology</subject><subject>Research Article</subject><issn>1998-0124</issn><issn>1998-0000</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LxDAQhoMouK7-AG_5A9V8tJv0KItfsOBlPYc0ndQsbbJM2gX_vV2qV-cywwvPwPsQcs_ZA2dMPWYuhCoLJkRR8VIW8oKseF3rgs1z-XdzUV6Tm5wPjG0EL_WK9HuLHYzQUoRu6u0YUqTJ0wgTphB9b4dhCU_B0mhjakLKoYu2B6Q-4cwdbcAQOzp-AXUQR7T9zOMJaP7OIww0xMOEAfItufK2z3D3u9fk8-V5v30rdh-v79unXeEE12OheN1sQIFrmPa2bL1XbaPLjbdaMudqBlwp69pKVrVQtdBVXYFiwklvvdNMrglf_jpMOSN4c8QwWPw2nJmzLrPoMrMuc9Zl5MyIhcnHcxlAc0gTzjXzP9APUgxw5g</recordid><startdate>20230201</startdate><enddate>20230201</enddate><creator>Sun, Xiaoru</creator><creator>Ruan, Huitong</creator><creator>Liu, Qidong</creator><creator>Cao, Silu</creator><creator>Jing, Qi</creator><creator>Xu, Yaru</creator><creator>Xiong, Lize</creator><creator>Cui, Wenguo</creator><creator>Li, Cheng</creator><general>Tsinghua University Press</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20230201</creationdate><title>Targeted regulation of neuroinflammation via nanobiosignaler for repairing the central nerve system injuries</title><author>Sun, Xiaoru ; Ruan, Huitong ; Liu, Qidong ; Cao, Silu ; Jing, Qi ; Xu, Yaru ; Xiong, Lize ; Cui, Wenguo ; Li, Cheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c218t-719b6e7ecb08fa4dff7db846fa830cc90e177acd535927928595e702c3fafc803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Atomic/Molecular Structure and Spectra</topic><topic>Biomedicine</topic><topic>Biotechnology</topic><topic>Chemistry and Materials Science</topic><topic>Condensed Matter Physics</topic><topic>Materials Science</topic><topic>Nanotechnology</topic><topic>Research Article</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sun, Xiaoru</creatorcontrib><creatorcontrib>Ruan, Huitong</creatorcontrib><creatorcontrib>Liu, Qidong</creatorcontrib><creatorcontrib>Cao, Silu</creatorcontrib><creatorcontrib>Jing, Qi</creatorcontrib><creatorcontrib>Xu, Yaru</creatorcontrib><creatorcontrib>Xiong, Lize</creatorcontrib><creatorcontrib>Cui, Wenguo</creatorcontrib><creatorcontrib>Li, Cheng</creatorcontrib><collection>CrossRef</collection><jtitle>Nano research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sun, Xiaoru</au><au>Ruan, Huitong</au><au>Liu, Qidong</au><au>Cao, Silu</au><au>Jing, Qi</au><au>Xu, Yaru</au><au>Xiong, Lize</au><au>Cui, Wenguo</au><au>Li, Cheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Targeted regulation of neuroinflammation via nanobiosignaler for repairing the central nerve system injuries</atitle><jtitle>Nano research</jtitle><stitle>Nano Res</stitle><date>2023-02-01</date><risdate>2023</risdate><volume>16</volume><issue>2</issue><spage>2938</spage><epage>2948</epage><pages>2938-2948</pages><issn>1998-0124</issn><eissn>1998-0000</eissn><abstract>Neuroinflammation, commonly associated with various central nervous system (CNS) diseases such as postoperative cognitive dysfunction (POCD), is primarily mediated by the disruption of biological signals in microglia. However, the effective treatment of CNS diseases remains an ongoing challenge as biological signals show limited microglia-targeting effect. In this study, taking advantage of the highly expressed lipoprotein receptor-related protein-1 (LRP1) on the microglia, a nanobiosignal delivery system modified by LRP1 high-affinity peptide ligand RAP12 (RAP: receptor-associated protein) was constructed to specifically regulate neuroinflammation via targeting microglia. The uptake of the RAP12 modified-nanobiosignaler by microglia increased significantly, indicating its microglia-targeting ability. Both
in vitro/vivo
studies proved that the “nanobiosignaler” significantly reduced the secretion of pro-inflammatory cytokines, induced specific M2 (anti-inflammatory type) microglia differentiation, and remarkably alleviated cognitive function impairment in the mice model when compared with unmodified groups. It was indicated that the “nanobiosignaler” could target microglia to deliver the biological signal and inhibit the excessive activation of microglia. Overall, the cell-targeted biological signal transmission system inspired by “nanobiosignaler” has broad application prospects in the future.</abstract><cop>Beijing</cop><pub>Tsinghua University Press</pub><doi>10.1007/s12274-022-5143-3</doi><tpages>11</tpages></addata></record> |
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subjects | Atomic/Molecular Structure and Spectra Biomedicine Biotechnology Chemistry and Materials Science Condensed Matter Physics Materials Science Nanotechnology Research Article |
title | Targeted regulation of neuroinflammation via nanobiosignaler for repairing the central nerve system injuries |
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