Effects of fibroin microcarriers on inflammation and regeneration of deep skin wounds in mice
The process of tissue regeneration following damage takes place with direct participation of the immune system. The use of biomaterials as scaffolds to facilitate healing of skin wounds is a new and interesting area of regenerative medicine and biomedical research. In many ways, the regenerative pot...
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Veröffentlicht in: | Biochemistry (Moscow) 2016-11, Vol.81 (11), p.1251-1260 |
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creator | Arkhipova, A. Y. Nosenko, M. A. Malyuchenko, N. V. Zvartsev, R. V. Moisenovich, A. M. Zhdanova, A. S. Vasil’eva, T. V. Gorshkova, E. A. Agapov, I. I. Drutskaya, M. S. Nedospasov, S. A. Moisenovich, M. M. |
description | The process of tissue regeneration following damage takes place with direct participation of the immune system. The use of biomaterials as scaffolds to facilitate healing of skin wounds is a new and interesting area of regenerative medicine and biomedical research. In many ways, the regenerative potential of biological material is related to its ability to modulate the inflammatory response. At the same time, all foreign materials, once implanted into a living tissue, to varying degree cause an immune reaction. The modern approach to the development of bioengineered structures for applications in regenerative medicine should be directed toward using the properties of the inflammatory response that improve healing, but do not lead to negative chronic manifestations. In this work, we studied the effect of microcarriers comprised of either fibroin or fibroin supplemented with gelatin on the dynamics of the healing, as well as inflammation, during regeneration of deep skin wounds in mice. We found that subcutaneous administration of microcarriers to the wound area resulted in uniform contraction of the wounds in mice in our experimental model, and microcarrier particles induced the infiltration of immune cells. This was associated with increased expression of proinflammatory cytokines TNF, IL-6, IL-1β, and chemokines CXCL1 and CXCL2, which contributed to full functional recovery of the injured area and the absence of fibrosis as compared to the control group. |
doi_str_mv | 10.1134/S0006297916110031 |
format | Article |
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Y. ; Nosenko, M. A. ; Malyuchenko, N. V. ; Zvartsev, R. V. ; Moisenovich, A. M. ; Zhdanova, A. S. ; Vasil’eva, T. V. ; Gorshkova, E. A. ; Agapov, I. I. ; Drutskaya, M. S. ; Nedospasov, S. A. ; Moisenovich, M. M.</creator><creatorcontrib>Arkhipova, A. Y. ; Nosenko, M. A. ; Malyuchenko, N. V. ; Zvartsev, R. V. ; Moisenovich, A. M. ; Zhdanova, A. S. ; Vasil’eva, T. V. ; Gorshkova, E. A. ; Agapov, I. I. ; Drutskaya, M. S. ; Nedospasov, S. A. ; Moisenovich, M. M.</creatorcontrib><description>The process of tissue regeneration following damage takes place with direct participation of the immune system. The use of biomaterials as scaffolds to facilitate healing of skin wounds is a new and interesting area of regenerative medicine and biomedical research. In many ways, the regenerative potential of biological material is related to its ability to modulate the inflammatory response. At the same time, all foreign materials, once implanted into a living tissue, to varying degree cause an immune reaction. The modern approach to the development of bioengineered structures for applications in regenerative medicine should be directed toward using the properties of the inflammatory response that improve healing, but do not lead to negative chronic manifestations. In this work, we studied the effect of microcarriers comprised of either fibroin or fibroin supplemented with gelatin on the dynamics of the healing, as well as inflammation, during regeneration of deep skin wounds in mice. We found that subcutaneous administration of microcarriers to the wound area resulted in uniform contraction of the wounds in mice in our experimental model, and microcarrier particles induced the infiltration of immune cells. This was associated with increased expression of proinflammatory cytokines TNF, IL-6, IL-1β, and chemokines CXCL1 and CXCL2, which contributed to full functional recovery of the injured area and the absence of fibrosis as compared to the control group.</description><identifier>ISSN: 0006-2979</identifier><identifier>EISSN: 1608-3040</identifier><identifier>DOI: 10.1134/S0006297916110031</identifier><identifier>PMID: 27914451</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Animals ; Biochemistry ; Biomaterials ; Biomedical and Life Sciences ; Biomedicine ; Bioorganic Chemistry ; Cytokines ; Cytokines - immunology ; Female ; Fibroins - pharmacology ; Immune system ; Life Sciences ; Mice ; Microbiology ; Molecular and Cellular Mechanisms of Inflammation (Special Issue) Guest Editors S. A. Nedospasov and D. V. Kuprash ; Rodents ; Skin ; Skin - immunology ; Skin - pathology ; Tissue engineering ; Wound healing ; Wound Healing - drug effects ; Wound Healing - immunology ; Wounds and Injuries - drug therapy ; Wounds and Injuries - immunology ; Wounds and Injuries - pathology</subject><ispartof>Biochemistry (Moscow), 2016-11, Vol.81 (11), p.1251-1260</ispartof><rights>Pleiades Publishing, Ltd. 2016</rights><rights>COPYRIGHT 2016 Springer</rights><rights>Biochemistry (Moscow) is a copyright of Springer, 2016.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c472t-1439ba0e705c983d193732d78d62d2846943dca632695b802e3b5b33adc0f1b3</citedby><cites>FETCH-LOGICAL-c472t-1439ba0e705c983d193732d78d62d2846943dca632695b802e3b5b33adc0f1b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S0006297916110031$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S0006297916110031$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27914451$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Arkhipova, A. Y.</creatorcontrib><creatorcontrib>Nosenko, M. A.</creatorcontrib><creatorcontrib>Malyuchenko, N. V.</creatorcontrib><creatorcontrib>Zvartsev, R. V.</creatorcontrib><creatorcontrib>Moisenovich, A. M.</creatorcontrib><creatorcontrib>Zhdanova, A. S.</creatorcontrib><creatorcontrib>Vasil’eva, T. V.</creatorcontrib><creatorcontrib>Gorshkova, E. A.</creatorcontrib><creatorcontrib>Agapov, I. I.</creatorcontrib><creatorcontrib>Drutskaya, M. S.</creatorcontrib><creatorcontrib>Nedospasov, S. A.</creatorcontrib><creatorcontrib>Moisenovich, M. M.</creatorcontrib><title>Effects of fibroin microcarriers on inflammation and regeneration of deep skin wounds in mice</title><title>Biochemistry (Moscow)</title><addtitle>Biochemistry Moscow</addtitle><addtitle>Biochemistry (Mosc)</addtitle><description>The process of tissue regeneration following damage takes place with direct participation of the immune system. The use of biomaterials as scaffolds to facilitate healing of skin wounds is a new and interesting area of regenerative medicine and biomedical research. In many ways, the regenerative potential of biological material is related to its ability to modulate the inflammatory response. At the same time, all foreign materials, once implanted into a living tissue, to varying degree cause an immune reaction. The modern approach to the development of bioengineered structures for applications in regenerative medicine should be directed toward using the properties of the inflammatory response that improve healing, but do not lead to negative chronic manifestations. In this work, we studied the effect of microcarriers comprised of either fibroin or fibroin supplemented with gelatin on the dynamics of the healing, as well as inflammation, during regeneration of deep skin wounds in mice. We found that subcutaneous administration of microcarriers to the wound area resulted in uniform contraction of the wounds in mice in our experimental model, and microcarrier particles induced the infiltration of immune cells. This was associated with increased expression of proinflammatory cytokines TNF, IL-6, IL-1β, and chemokines CXCL1 and CXCL2, which contributed to full functional recovery of the injured area and the absence of fibrosis as compared to the control group.</description><subject>Animals</subject><subject>Biochemistry</subject><subject>Biomaterials</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Bioorganic Chemistry</subject><subject>Cytokines</subject><subject>Cytokines - immunology</subject><subject>Female</subject><subject>Fibroins - pharmacology</subject><subject>Immune system</subject><subject>Life Sciences</subject><subject>Mice</subject><subject>Microbiology</subject><subject>Molecular and Cellular Mechanisms of Inflammation (Special Issue) Guest Editors S. A. Nedospasov and D. V. Kuprash</subject><subject>Rodents</subject><subject>Skin</subject><subject>Skin - immunology</subject><subject>Skin - pathology</subject><subject>Tissue engineering</subject><subject>Wound healing</subject><subject>Wound Healing - drug effects</subject><subject>Wound Healing - immunology</subject><subject>Wounds and Injuries - drug therapy</subject><subject>Wounds and Injuries - immunology</subject><subject>Wounds and Injuries - pathology</subject><issn>0006-2979</issn><issn>1608-3040</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNkUtr3TAQhUVpaW6T_oBuiqGbbpzoZVlahpCmhUAXzbYYWRpflNrSrWRT-u87xnn0CUULoTnfOWhmCHnF6CljQp59opQqblrDFGOUCvaE7JiiuhZU0qdkt8r1qh-RF6Xc4pNTI56TI44WKRu2I58vhwHcXKo0VEPocwqxmoLLydmcA2QUYhXiMNppsnPAh42-yrCHCHkroNMDHKryBb3f0hJ9qbYUOCHPBjsWeHl3H5Obd5c3F-_r649XHy7Or2snWz7XTArTWwotbZzRwjMjWsF9q73inmupjBTeWSW4Mk2vKQfRN70Q1js6sF4ck7db7CGnrwuUuZtCcTCONkJaSsd0Q1sM0eI_UKko1zgfRN_8ht6mJUfsY6W45Nwo80jt7QgdTirN2bo1tDtvpG6UoM1Knf6FwuMB55QiDAHrvxjYZsBVlJJh6A45TDZ_7xjt1uV3fywfPa_vPrz0E_gHx_22EeAbUFCKe8g_dfTP1B9Q8bUr</recordid><startdate>20161101</startdate><enddate>20161101</enddate><creator>Arkhipova, A. 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Y. ; Nosenko, M. A. ; Malyuchenko, N. V. ; Zvartsev, R. V. ; Moisenovich, A. M. ; Zhdanova, A. S. ; Vasil’eva, T. V. ; Gorshkova, E. A. ; Agapov, I. I. ; Drutskaya, M. S. ; Nedospasov, S. A. ; Moisenovich, M. M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c472t-1439ba0e705c983d193732d78d62d2846943dca632695b802e3b5b33adc0f1b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Biochemistry</topic><topic>Biomaterials</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Bioorganic Chemistry</topic><topic>Cytokines</topic><topic>Cytokines - immunology</topic><topic>Female</topic><topic>Fibroins - pharmacology</topic><topic>Immune system</topic><topic>Life Sciences</topic><topic>Mice</topic><topic>Microbiology</topic><topic>Molecular and Cellular Mechanisms of Inflammation (Special Issue) Guest Editors S. A. Nedospasov and D. V. Kuprash</topic><topic>Rodents</topic><topic>Skin</topic><topic>Skin - immunology</topic><topic>Skin - pathology</topic><topic>Tissue engineering</topic><topic>Wound healing</topic><topic>Wound Healing - drug effects</topic><topic>Wound Healing - immunology</topic><topic>Wounds and Injuries - drug therapy</topic><topic>Wounds and Injuries - immunology</topic><topic>Wounds and Injuries - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arkhipova, A. Y.</creatorcontrib><creatorcontrib>Nosenko, M. A.</creatorcontrib><creatorcontrib>Malyuchenko, N. V.</creatorcontrib><creatorcontrib>Zvartsev, R. V.</creatorcontrib><creatorcontrib>Moisenovich, A. M.</creatorcontrib><creatorcontrib>Zhdanova, A. S.</creatorcontrib><creatorcontrib>Vasil’eva, T. V.</creatorcontrib><creatorcontrib>Gorshkova, E. A.</creatorcontrib><creatorcontrib>Agapov, I. I.</creatorcontrib><creatorcontrib>Drutskaya, M. 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Y.</au><au>Nosenko, M. A.</au><au>Malyuchenko, N. V.</au><au>Zvartsev, R. V.</au><au>Moisenovich, A. M.</au><au>Zhdanova, A. S.</au><au>Vasil’eva, T. V.</au><au>Gorshkova, E. A.</au><au>Agapov, I. I.</au><au>Drutskaya, M. S.</au><au>Nedospasov, S. A.</au><au>Moisenovich, M. M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of fibroin microcarriers on inflammation and regeneration of deep skin wounds in mice</atitle><jtitle>Biochemistry (Moscow)</jtitle><stitle>Biochemistry Moscow</stitle><addtitle>Biochemistry (Mosc)</addtitle><date>2016-11-01</date><risdate>2016</risdate><volume>81</volume><issue>11</issue><spage>1251</spage><epage>1260</epage><pages>1251-1260</pages><issn>0006-2979</issn><eissn>1608-3040</eissn><abstract>The process of tissue regeneration following damage takes place with direct participation of the immune system. The use of biomaterials as scaffolds to facilitate healing of skin wounds is a new and interesting area of regenerative medicine and biomedical research. In many ways, the regenerative potential of biological material is related to its ability to modulate the inflammatory response. At the same time, all foreign materials, once implanted into a living tissue, to varying degree cause an immune reaction. The modern approach to the development of bioengineered structures for applications in regenerative medicine should be directed toward using the properties of the inflammatory response that improve healing, but do not lead to negative chronic manifestations. In this work, we studied the effect of microcarriers comprised of either fibroin or fibroin supplemented with gelatin on the dynamics of the healing, as well as inflammation, during regeneration of deep skin wounds in mice. We found that subcutaneous administration of microcarriers to the wound area resulted in uniform contraction of the wounds in mice in our experimental model, and microcarrier particles induced the infiltration of immune cells. This was associated with increased expression of proinflammatory cytokines TNF, IL-6, IL-1β, and chemokines CXCL1 and CXCL2, which contributed to full functional recovery of the injured area and the absence of fibrosis as compared to the control group.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><pmid>27914451</pmid><doi>10.1134/S0006297916110031</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Biochemistry Biomaterials Biomedical and Life Sciences Biomedicine Bioorganic Chemistry Cytokines Cytokines - immunology Female Fibroins - pharmacology Immune system Life Sciences Mice Microbiology Molecular and Cellular Mechanisms of Inflammation (Special Issue) Guest Editors S. A. Nedospasov and D. V. Kuprash Rodents Skin Skin - immunology Skin - pathology Tissue engineering Wound healing Wound Healing - drug effects Wound Healing - immunology Wounds and Injuries - drug therapy Wounds and Injuries - immunology Wounds and Injuries - pathology |
title | Effects of fibroin microcarriers on inflammation and regeneration of deep skin wounds in mice |
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