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M2 microglia-derived exosomes promote vascular remodeling in diabetic retinopathy
Diabetic retinopathy (DR) is a vision-threatening diabetic complication that is characterized by microvasculature impairment and immune dysfunction. The present study demonstrated that M2 microglia intensively participated in retinal microangiopathy in human diabetic proliferative membranes, mice re...
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Published in: | Journal of nanobiotechnology 2024-02, Vol.22 (1), p.56-56, Article 56 |
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creator | Wang, Xingxing Xu, Changlin Bian, Cunxin Ge, Pengfei Lei, Jie Wang, Jingfan Xiao, Tianhao Fan, Yuanyuan Gu, Qinyuan Li, Hong-Ying Xu, Jingyi Hu, Zizhong Xie, Ping |
description | Diabetic retinopathy (DR) is a vision-threatening diabetic complication that is characterized by microvasculature impairment and immune dysfunction. The present study demonstrated that M2 microglia intensively participated in retinal microangiopathy in human diabetic proliferative membranes, mice retinas, retinas of mice with oxygen-induced retinopathy (OIR) mice, and retinas of streptozotocin-induced DR mice. Further in vivo and in vitro experiments showed that exosomes derived from M2 polarized microglia (M2-exo) could reduce pericyte apoptosis and promote endothelial cell proliferation, thereby promoting vascular remodeling and reducing vascular leakage from the diabetic retina. These effects were further enhanced by M2-exo that facilitated M2 polarization of retinal microglia. Collectively, the study demonstrated the capability of M2-exo to induce retinal microvascular remodeling, which may provide a new therapeutic strategy for the treatment of DR. |
doi_str_mv | 10.1186/s12951-024-02330-w |
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The present study demonstrated that M2 microglia intensively participated in retinal microangiopathy in human diabetic proliferative membranes, mice retinas, retinas of mice with oxygen-induced retinopathy (OIR) mice, and retinas of streptozotocin-induced DR mice. Further in vivo and in vitro experiments showed that exosomes derived from M2 polarized microglia (M2-exo) could reduce pericyte apoptosis and promote endothelial cell proliferation, thereby promoting vascular remodeling and reducing vascular leakage from the diabetic retina. These effects were further enhanced by M2-exo that facilitated M2 polarization of retinal microglia. Collectively, the study demonstrated the capability of M2-exo to induce retinal microvascular remodeling, which may provide a new therapeutic strategy for the treatment of DR.</description><identifier>ISSN: 1477-3155</identifier><identifier>EISSN: 1477-3155</identifier><identifier>DOI: 10.1186/s12951-024-02330-w</identifier><identifier>PMID: 38336783</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Angiogenesis ; Apoptosis ; Care and treatment ; Cell growth ; Cell proliferation ; Cytokines ; Diabetes ; Diabetes mellitus ; Diabetic retinopathy ; Diagnosis ; Digital cameras ; Disease susceptibility ; Endothelial cells ; Evaluation ; Exosomes ; Glucose ; Homeostasis ; Metabolites ; Microglia ; Microscopy ; Microvasculature ; Permeability ; Retina ; Retinopathy ; Streptozocin</subject><ispartof>Journal of nanobiotechnology, 2024-02, Vol.22 (1), p.56-56, Article 56</ispartof><rights>2024. The Author(s).</rights><rights>COPYRIGHT 2024 BioMed Central Ltd.</rights><rights>2024. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c542t-a604da7093913ad470547b96a306915b5fdebc82996fd1b0970385943bea11513</citedby><cites>FETCH-LOGICAL-c542t-a604da7093913ad470547b96a306915b5fdebc82996fd1b0970385943bea11513</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2925656235?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,37013,44590</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38336783$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Xingxing</creatorcontrib><creatorcontrib>Xu, Changlin</creatorcontrib><creatorcontrib>Bian, Cunxin</creatorcontrib><creatorcontrib>Ge, Pengfei</creatorcontrib><creatorcontrib>Lei, Jie</creatorcontrib><creatorcontrib>Wang, Jingfan</creatorcontrib><creatorcontrib>Xiao, Tianhao</creatorcontrib><creatorcontrib>Fan, Yuanyuan</creatorcontrib><creatorcontrib>Gu, Qinyuan</creatorcontrib><creatorcontrib>Li, Hong-Ying</creatorcontrib><creatorcontrib>Xu, Jingyi</creatorcontrib><creatorcontrib>Hu, Zizhong</creatorcontrib><creatorcontrib>Xie, Ping</creatorcontrib><title>M2 microglia-derived exosomes promote vascular remodeling in diabetic retinopathy</title><title>Journal of nanobiotechnology</title><addtitle>J Nanobiotechnology</addtitle><description>Diabetic retinopathy (DR) is a vision-threatening diabetic complication that is characterized by microvasculature impairment and immune dysfunction. The present study demonstrated that M2 microglia intensively participated in retinal microangiopathy in human diabetic proliferative membranes, mice retinas, retinas of mice with oxygen-induced retinopathy (OIR) mice, and retinas of streptozotocin-induced DR mice. Further in vivo and in vitro experiments showed that exosomes derived from M2 polarized microglia (M2-exo) could reduce pericyte apoptosis and promote endothelial cell proliferation, thereby promoting vascular remodeling and reducing vascular leakage from the diabetic retina. These effects were further enhanced by M2-exo that facilitated M2 polarization of retinal microglia. Collectively, the study demonstrated the capability of M2-exo to induce retinal microvascular remodeling, which may provide a new therapeutic strategy for the treatment of DR.</description><subject>Angiogenesis</subject><subject>Apoptosis</subject><subject>Care and treatment</subject><subject>Cell growth</subject><subject>Cell proliferation</subject><subject>Cytokines</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetic retinopathy</subject><subject>Diagnosis</subject><subject>Digital cameras</subject><subject>Disease susceptibility</subject><subject>Endothelial cells</subject><subject>Evaluation</subject><subject>Exosomes</subject><subject>Glucose</subject><subject>Homeostasis</subject><subject>Metabolites</subject><subject>Microglia</subject><subject>Microscopy</subject><subject>Microvasculature</subject><subject>Permeability</subject><subject>Retina</subject><subject>Retinopathy</subject><subject>Streptozocin</subject><issn>1477-3155</issn><issn>1477-3155</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkttu1DAQhiMEoqXwAlygSNzQixSfHV9WFZSVihCna2sST4JXSbzYSQ9vj3e3FBYhy7I1-uYfz_gvipeUnFFaq7eJMiNpRZjIm3NS3TwqjqnQuuJUysd_3Y-KZymtCWFMMPG0OOI150rX_Lj4_JGVo29j6AcPlcPor9GVeBtSGDGVmxjGMGN5DaldBohlxDE4HPzUl34qnYcGZ9_m8OynsIH5x93z4kkHQ8IX9-dJ8f39u28XH6qrT5eri_OrqpWCzRUoIhxoYrihHJzQRArdGAWcKENlIzuHTVszY1TnaEOMJryWRvAGgVJJ-Umx2uu6AGu7iX6EeGcDeLsLhNhbiPltA1ollDZOsJYaLhpNa1krpRx3tM2a2GWtN3ut3O_PBdNsR59aHAaYMCzJMsPkdnpkW_b1P-g6LHHKne4oJRXj8g_VQ67vpy7MEdqtqD3XdRYikpNMnf2Hysth_pMwYedz_CDh9CAhMzPezj0sKdnV1y-HLNuz-XNTitg9zIgSu_WP3fvHZv_YnX_sTU56dd_d0ozoHlJ-G4b_Aq6Lu8o</recordid><startdate>20240209</startdate><enddate>20240209</enddate><creator>Wang, Xingxing</creator><creator>Xu, Changlin</creator><creator>Bian, Cunxin</creator><creator>Ge, Pengfei</creator><creator>Lei, Jie</creator><creator>Wang, Jingfan</creator><creator>Xiao, Tianhao</creator><creator>Fan, Yuanyuan</creator><creator>Gu, Qinyuan</creator><creator>Li, Hong-Ying</creator><creator>Xu, Jingyi</creator><creator>Hu, Zizhong</creator><creator>Xie, Ping</creator><general>BioMed Central Ltd</general><general>BioMed 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microglia-derived exosomes promote vascular remodeling in diabetic retinopathy</title><author>Wang, Xingxing ; Xu, Changlin ; Bian, Cunxin ; Ge, Pengfei ; Lei, Jie ; Wang, Jingfan ; Xiao, Tianhao ; Fan, Yuanyuan ; Gu, Qinyuan ; Li, Hong-Ying ; Xu, Jingyi ; Hu, Zizhong ; Xie, Ping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c542t-a604da7093913ad470547b96a306915b5fdebc82996fd1b0970385943bea11513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Angiogenesis</topic><topic>Apoptosis</topic><topic>Care and treatment</topic><topic>Cell growth</topic><topic>Cell proliferation</topic><topic>Cytokines</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetic retinopathy</topic><topic>Diagnosis</topic><topic>Digital cameras</topic><topic>Disease susceptibility</topic><topic>Endothelial 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Zizhong</au><au>Xie, Ping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>M2 microglia-derived exosomes promote vascular remodeling in diabetic retinopathy</atitle><jtitle>Journal of nanobiotechnology</jtitle><addtitle>J Nanobiotechnology</addtitle><date>2024-02-09</date><risdate>2024</risdate><volume>22</volume><issue>1</issue><spage>56</spage><epage>56</epage><pages>56-56</pages><artnum>56</artnum><issn>1477-3155</issn><eissn>1477-3155</eissn><abstract>Diabetic retinopathy (DR) is a vision-threatening diabetic complication that is characterized by microvasculature impairment and immune dysfunction. The present study demonstrated that M2 microglia intensively participated in retinal microangiopathy in human diabetic proliferative membranes, mice retinas, retinas of mice with oxygen-induced retinopathy (OIR) mice, and retinas of streptozotocin-induced DR mice. Further in vivo and in vitro experiments showed that exosomes derived from M2 polarized microglia (M2-exo) could reduce pericyte apoptosis and promote endothelial cell proliferation, thereby promoting vascular remodeling and reducing vascular leakage from the diabetic retina. These effects were further enhanced by M2-exo that facilitated M2 polarization of retinal microglia. Collectively, the study demonstrated the capability of M2-exo to induce retinal microvascular remodeling, which may provide a new therapeutic strategy for the treatment of DR.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>38336783</pmid><doi>10.1186/s12951-024-02330-w</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Angiogenesis Apoptosis Care and treatment Cell growth Cell proliferation Cytokines Diabetes Diabetes mellitus Diabetic retinopathy Diagnosis Digital cameras Disease susceptibility Endothelial cells Evaluation Exosomes Glucose Homeostasis Metabolites Microglia Microscopy Microvasculature Permeability Retina Retinopathy Streptozocin |
title | M2 microglia-derived exosomes promote vascular remodeling in diabetic retinopathy |
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