Controllable Adaptive Molybdate‐Oligosaccharide Nanoparticles Regulate M2 Macrophage Mitochondrial Function and Promote Angiogenesis via PI3K/HIF‐1α/VEGF Pathway to Accelerate Diabetic Wound Healing (Adv. Healthcare Mater. 3/2024)

Molybdate‐Oligosaccharide Nanosystem The powerful molybdate‐oligosaccharide nanosystem (CMO) exhibit pH‐responsive release Mo2+ and oligosaccharide to enhance mitochondrial function and facilitate the transition of macrophages from M1 to M2 phenotype. In article 2302256, Xiuhong Huang, Shaohong Huan...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Advanced healthcare materials 2024-01, Vol.13 (3), p.n/a
Hauptverfasser: Huang, Xiuhong, Zheng, Liqin, Zhou, Yueshan, Hu, Shaonan, Ning, Wancheng, Li, Simin, Lin, Ziling, Huang, Shaohong
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page n/a
container_issue 3
container_start_page
container_title Advanced healthcare materials
container_volume 13
creator Huang, Xiuhong
Zheng, Liqin
Zhou, Yueshan
Hu, Shaonan
Ning, Wancheng
Li, Simin
Lin, Ziling
Huang, Shaohong
description Molybdate‐Oligosaccharide Nanosystem The powerful molybdate‐oligosaccharide nanosystem (CMO) exhibit pH‐responsive release Mo2+ and oligosaccharide to enhance mitochondrial function and facilitate the transition of macrophages from M1 to M2 phenotype. In article 2302256, Xiuhong Huang, Shaohong Huang, and co‐workers show that within an anti‐inflammatory microenvironment, CMO promote angiogenesis through activation of the PI3K/HIF‐1α/VEGF pathway. Such a pH‐responsive nanosystem with immunomodulatory properties and angiogenesis‐ and mitochondrial‐promotion capacity presents a promising potential for diabetic wounds repair.
doi_str_mv 10.1002/adhm.202470018
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2918716432</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2918716432</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1578-71b8dc0e05d8d9543511081752c8c3378392ba81fda14bc76f4fe50b8842446e3</originalsourceid><addsrcrecordid>eNqFkU1u2zAQhYWiBRqk2XZNoJt2YZmk_qil4MSxkbgxiv4shRFJSQxoUiUlB971CL1KL5JDdNtLlK6LdFluhgN8b95gXhS9JjgmGNM5iH4XU0zTAmPCnkVnlJR0RvOsfP70T_HL6ML7exxenpGckbPo18Ka0VmtodESVQKGUe0l2lh9aASM8ue373daddYD5z04JSR6D8YO4EbFtfTog-wmHUC0oWgD3Nmhhy50arS8t0Y4BRotJ8NHZQ0CI9DW2Z0Ngsp0ynbSSK882itA23VyM1-tl8GTPP6Yf766XqItjP0DHNBoUcW51NIdvS4VNDIsgL7YKUxcSdDKdOhtJfbxn27sObiwRYBdjJL58TLvXkUvWtBeXvyt59Gn5dXHxWp2e3e9XlS3M06ygs0K0jDBscSZYKLM0iQjBDNSZJQzniQFS0raACOtAJI2vMjbtJUZbhhLaZrmMjmP3pzmDs5-naQf63s7ORMsa1oSVpA8TWig4hMVbua9k209OLUDd6gJro-Z1sdM66dMg6A8CR6Ulof_0HV1udr80_4GuZKpCA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2918716432</pqid></control><display><type>article</type><title>Controllable Adaptive Molybdate‐Oligosaccharide Nanoparticles Regulate M2 Macrophage Mitochondrial Function and Promote Angiogenesis via PI3K/HIF‐1α/VEGF Pathway to Accelerate Diabetic Wound Healing (Adv. Healthcare Mater. 3/2024)</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Huang, Xiuhong ; Zheng, Liqin ; Zhou, Yueshan ; Hu, Shaonan ; Ning, Wancheng ; Li, Simin ; Lin, Ziling ; Huang, Shaohong</creator><creatorcontrib>Huang, Xiuhong ; Zheng, Liqin ; Zhou, Yueshan ; Hu, Shaonan ; Ning, Wancheng ; Li, Simin ; Lin, Ziling ; Huang, Shaohong</creatorcontrib><description>Molybdate‐Oligosaccharide Nanosystem The powerful molybdate‐oligosaccharide nanosystem (CMO) exhibit pH‐responsive release Mo2+ and oligosaccharide to enhance mitochondrial function and facilitate the transition of macrophages from M1 to M2 phenotype. In article 2302256, Xiuhong Huang, Shaohong Huang, and co‐workers show that within an anti‐inflammatory microenvironment, CMO promote angiogenesis through activation of the PI3K/HIF‐1α/VEGF pathway. Such a pH‐responsive nanosystem with immunomodulatory properties and angiogenesis‐ and mitochondrial‐promotion capacity presents a promising potential for diabetic wounds repair.</description><identifier>ISSN: 2192-2640</identifier><identifier>EISSN: 2192-2659</identifier><identifier>DOI: 10.1002/adhm.202470018</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>1-Phosphatidylinositol 3-kinase ; Angiogenesis ; Controllability ; Diabetes mellitus ; Immunomodulation ; Inflammation ; Macrophages ; Mitochondria ; Molybdate ; Nanoparticles ; Oligosaccharides ; Phenotypes ; Vascular endothelial growth factor ; Wound healing</subject><ispartof>Advanced healthcare materials, 2024-01, Vol.13 (3), p.n/a</ispartof><rights>2024 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fadhm.202470018$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fadhm.202470018$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Huang, Xiuhong</creatorcontrib><creatorcontrib>Zheng, Liqin</creatorcontrib><creatorcontrib>Zhou, Yueshan</creatorcontrib><creatorcontrib>Hu, Shaonan</creatorcontrib><creatorcontrib>Ning, Wancheng</creatorcontrib><creatorcontrib>Li, Simin</creatorcontrib><creatorcontrib>Lin, Ziling</creatorcontrib><creatorcontrib>Huang, Shaohong</creatorcontrib><title>Controllable Adaptive Molybdate‐Oligosaccharide Nanoparticles Regulate M2 Macrophage Mitochondrial Function and Promote Angiogenesis via PI3K/HIF‐1α/VEGF Pathway to Accelerate Diabetic Wound Healing (Adv. Healthcare Mater. 3/2024)</title><title>Advanced healthcare materials</title><description>Molybdate‐Oligosaccharide Nanosystem The powerful molybdate‐oligosaccharide nanosystem (CMO) exhibit pH‐responsive release Mo2+ and oligosaccharide to enhance mitochondrial function and facilitate the transition of macrophages from M1 to M2 phenotype. In article 2302256, Xiuhong Huang, Shaohong Huang, and co‐workers show that within an anti‐inflammatory microenvironment, CMO promote angiogenesis through activation of the PI3K/HIF‐1α/VEGF pathway. Such a pH‐responsive nanosystem with immunomodulatory properties and angiogenesis‐ and mitochondrial‐promotion capacity presents a promising potential for diabetic wounds repair.</description><subject>1-Phosphatidylinositol 3-kinase</subject><subject>Angiogenesis</subject><subject>Controllability</subject><subject>Diabetes mellitus</subject><subject>Immunomodulation</subject><subject>Inflammation</subject><subject>Macrophages</subject><subject>Mitochondria</subject><subject>Molybdate</subject><subject>Nanoparticles</subject><subject>Oligosaccharides</subject><subject>Phenotypes</subject><subject>Vascular endothelial growth factor</subject><subject>Wound healing</subject><issn>2192-2640</issn><issn>2192-2659</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkU1u2zAQhYWiBRqk2XZNoJt2YZmk_qil4MSxkbgxiv4shRFJSQxoUiUlB971CL1KL5JDdNtLlK6LdFluhgN8b95gXhS9JjgmGNM5iH4XU0zTAmPCnkVnlJR0RvOsfP70T_HL6ML7exxenpGckbPo18Ka0VmtodESVQKGUe0l2lh9aASM8ue373daddYD5z04JSR6D8YO4EbFtfTog-wmHUC0oWgD3Nmhhy50arS8t0Y4BRotJ8NHZQ0CI9DW2Z0Ngsp0ynbSSK882itA23VyM1-tl8GTPP6Yf766XqItjP0DHNBoUcW51NIdvS4VNDIsgL7YKUxcSdDKdOhtJfbxn27sObiwRYBdjJL58TLvXkUvWtBeXvyt59Gn5dXHxWp2e3e9XlS3M06ygs0K0jDBscSZYKLM0iQjBDNSZJQzniQFS0raACOtAJI2vMjbtJUZbhhLaZrmMjmP3pzmDs5-naQf63s7ORMsa1oSVpA8TWig4hMVbua9k209OLUDd6gJro-Z1sdM66dMg6A8CR6Ulof_0HV1udr80_4GuZKpCA</recordid><startdate>20240101</startdate><enddate>20240101</enddate><creator>Huang, Xiuhong</creator><creator>Zheng, Liqin</creator><creator>Zhou, Yueshan</creator><creator>Hu, Shaonan</creator><creator>Ning, Wancheng</creator><creator>Li, Simin</creator><creator>Lin, Ziling</creator><creator>Huang, Shaohong</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QP</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7T5</scope><scope>7TA</scope><scope>7TB</scope><scope>7TM</scope><scope>7TO</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>JG9</scope><scope>JQ2</scope><scope>K9.</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope></search><sort><creationdate>20240101</creationdate><title>Controllable Adaptive Molybdate‐Oligosaccharide Nanoparticles Regulate M2 Macrophage Mitochondrial Function and Promote Angiogenesis via PI3K/HIF‐1α/VEGF Pathway to Accelerate Diabetic Wound Healing (Adv. Healthcare Mater. 3/2024)</title><author>Huang, Xiuhong ; Zheng, Liqin ; Zhou, Yueshan ; Hu, Shaonan ; Ning, Wancheng ; Li, Simin ; Lin, Ziling ; Huang, Shaohong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1578-71b8dc0e05d8d9543511081752c8c3378392ba81fda14bc76f4fe50b8842446e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>1-Phosphatidylinositol 3-kinase</topic><topic>Angiogenesis</topic><topic>Controllability</topic><topic>Diabetes mellitus</topic><topic>Immunomodulation</topic><topic>Inflammation</topic><topic>Macrophages</topic><topic>Mitochondria</topic><topic>Molybdate</topic><topic>Nanoparticles</topic><topic>Oligosaccharides</topic><topic>Phenotypes</topic><topic>Vascular endothelial growth factor</topic><topic>Wound healing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Xiuhong</creatorcontrib><creatorcontrib>Zheng, Liqin</creatorcontrib><creatorcontrib>Zhou, Yueshan</creatorcontrib><creatorcontrib>Hu, Shaonan</creatorcontrib><creatorcontrib>Ning, Wancheng</creatorcontrib><creatorcontrib>Li, Simin</creatorcontrib><creatorcontrib>Lin, Ziling</creatorcontrib><creatorcontrib>Huang, Shaohong</creatorcontrib><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics &amp; Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Immunology Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical &amp; Transportation Engineering Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology &amp; Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts – Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><jtitle>Advanced healthcare materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Xiuhong</au><au>Zheng, Liqin</au><au>Zhou, Yueshan</au><au>Hu, Shaonan</au><au>Ning, Wancheng</au><au>Li, Simin</au><au>Lin, Ziling</au><au>Huang, Shaohong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Controllable Adaptive Molybdate‐Oligosaccharide Nanoparticles Regulate M2 Macrophage Mitochondrial Function and Promote Angiogenesis via PI3K/HIF‐1α/VEGF Pathway to Accelerate Diabetic Wound Healing (Adv. Healthcare Mater. 3/2024)</atitle><jtitle>Advanced healthcare materials</jtitle><date>2024-01-01</date><risdate>2024</risdate><volume>13</volume><issue>3</issue><epage>n/a</epage><issn>2192-2640</issn><eissn>2192-2659</eissn><abstract>Molybdate‐Oligosaccharide Nanosystem The powerful molybdate‐oligosaccharide nanosystem (CMO) exhibit pH‐responsive release Mo2+ and oligosaccharide to enhance mitochondrial function and facilitate the transition of macrophages from M1 to M2 phenotype. In article 2302256, Xiuhong Huang, Shaohong Huang, and co‐workers show that within an anti‐inflammatory microenvironment, CMO promote angiogenesis through activation of the PI3K/HIF‐1α/VEGF pathway. Such a pH‐responsive nanosystem with immunomodulatory properties and angiogenesis‐ and mitochondrial‐promotion capacity presents a promising potential for diabetic wounds repair.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/adhm.202470018</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2192-2640
ispartof Advanced healthcare materials, 2024-01, Vol.13 (3), p.n/a
issn 2192-2640
2192-2659
language eng
recordid cdi_proquest_journals_2918716432
source Wiley Online Library Journals Frontfile Complete
subjects 1-Phosphatidylinositol 3-kinase
Angiogenesis
Controllability
Diabetes mellitus
Immunomodulation
Inflammation
Macrophages
Mitochondria
Molybdate
Nanoparticles
Oligosaccharides
Phenotypes
Vascular endothelial growth factor
Wound healing
title Controllable Adaptive Molybdate‐Oligosaccharide Nanoparticles Regulate M2 Macrophage Mitochondrial Function and Promote Angiogenesis via PI3K/HIF‐1α/VEGF Pathway to Accelerate Diabetic Wound Healing (Adv. Healthcare Mater. 3/2024)
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T05%3A44%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Controllable%20Adaptive%20Molybdate%E2%80%90Oligosaccharide%20Nanoparticles%20Regulate%20M2%20Macrophage%20Mitochondrial%20Function%20and%20Promote%20Angiogenesis%20via%20PI3K/HIF%E2%80%901%CE%B1/VEGF%20Pathway%20to%20Accelerate%20Diabetic%20Wound%20Healing%20(Adv.%20Healthcare%20Mater.%203/2024)&rft.jtitle=Advanced%20healthcare%20materials&rft.au=Huang,%20Xiuhong&rft.date=2024-01-01&rft.volume=13&rft.issue=3&rft.epage=n/a&rft.issn=2192-2640&rft.eissn=2192-2659&rft_id=info:doi/10.1002/adhm.202470018&rft_dat=%3Cproquest_cross%3E2918716432%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2918716432&rft_id=info:pmid/&rfr_iscdi=true