Aloe vera peel-derived nanovesicles display anti-inflammatory properties and prevent myofibroblast differentiation
Aloe vera (AV) is a medicinal plant, most known for its beneficial effects on a variety of skin conditions. Its known active compounds include carbohydrates and flavonoids such as quercetin and kaempferol, among others. In the past decade, plant nanovesicles (NVs) have gained considerable interest a...
Gespeichert in:
Veröffentlicht in: | Phytomedicine (Stuttgart) 2024-01, Vol.122, p.155108-155108, Article 155108 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 155108 |
---|---|
container_issue | |
container_start_page | 155108 |
container_title | Phytomedicine (Stuttgart) |
container_volume | 122 |
creator | Ramírez, Orlando Pomareda, Florencia Olivares, Belén Huang, Ya-Lin Zavala, Gabriela Carrasco-Rojas, Javiera Álvarez, Simón Leiva-Sabadini, Camila Hidalgo, Valeria Romo, Pablo Sánchez, Matías Vargas, Ayleen Martínez, Jessica Aguayo, Sebastian Schuh, Christina M.A.P. |
description | Aloe vera (AV) is a medicinal plant, most known for its beneficial effects on a variety of skin conditions. Its known active compounds include carbohydrates and flavonoids such as quercetin and kaempferol, among others. In the past decade, plant nanovesicles (NVs) have gained considerable interest as interkingdom communicators, presenting an opportunity for clinical standardization of natural products. In this study, we aimed to assess the potential of AVpNVs for the treatment of burn wounds.
AVpNVs were isolated and characterized regarding vesicle yield (nanoparticle tracking analysis) and structure (transmission electron microscopy and atomic force microscopy), as well as their protein content with proteomics. We assessed key characteristics for treating burn wounds in vitro, such as the anti-inflammatory potential in LPS-stimulated macrophages and keratinocytes, and the effect of AVpNVs on myofibroblast differentiation and contraction.
AVpNVs presented a homogenous NV population, vesicular shape, and NV-associated protein markers. AVpNVs significantly decreased the secretion of pro-inflammatory cytokines TNFα, IL-1β, and IL-6. Furthermore, AVpNVs inhibited myofibroblast differentiation and significantly decreased their contractile potential in collagen matrices. Observed effects were linked to proteins identified in the isolates through proteomics analysis.
AVpNVs displayed characteristics as an inflammatory modulator, while simultaneously diminishing myofibroblast differentiation and contraction. Novel strategies for burn wound treatment seek to decrease scarring on a cellular and molecular level in the early stages of wound healing, which makes AVpNVs a promising candidate for future plant-vesicle-based treatments. |
doi_str_mv | 10.1016/j.phymed.2023.155108 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3154187592</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0944711323004683</els_id><sourcerecordid>3154187592</sourcerecordid><originalsourceid>FETCH-LOGICAL-c372t-93e1961d99056ee32bdc0cd9dce6d993201c4c59695a68e1b7c6666fa4ef17093</originalsourceid><addsrcrecordid>eNqFUctKBDEQDKLguvoHHuboZdb0vHMRFvEFC14UvIVs0oNZMsmYxIH5e7OMZ-1DN11UFd0UIddAN0ChuT1sxs95QLUpaFFuoK6BdidkBQ10OWX1xylZUVZVeQtQnpOLEA6UQsVauiJ-axxmE3qRjYgmV-j1hCqzwroJg5YGQ6Z0GI2YM2GjzrXtjRgGEZ2fs9G7EX3UiSSsSitOaGM2zK7Xe-_2RoSY5H2PPuFaRO3sJTnrhQl49TvX5P3x4e3-Od-9Pr3cb3e5LNsi5qxEYA0oxmjdIJbFXkkqFVMSmwSWBQVZyZo1rBZNh7BvZZOqFxX20FJWrsnN4puO_PrGEPmgg0RjhEX3HXgJdQVdW7PiX2rRtV3Bjj1Rq4UqvQvBY89HrwfhZw6UH9PgB76kwY9p8CWNJLtbZJg-njR6HqRGK1FpjzJy5fTfBj97LZfd</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2878292878</pqid></control><display><type>article</type><title>Aloe vera peel-derived nanovesicles display anti-inflammatory properties and prevent myofibroblast differentiation</title><source>Elsevier ScienceDirect Journals</source><creator>Ramírez, Orlando ; Pomareda, Florencia ; Olivares, Belén ; Huang, Ya-Lin ; Zavala, Gabriela ; Carrasco-Rojas, Javiera ; Álvarez, Simón ; Leiva-Sabadini, Camila ; Hidalgo, Valeria ; Romo, Pablo ; Sánchez, Matías ; Vargas, Ayleen ; Martínez, Jessica ; Aguayo, Sebastian ; Schuh, Christina M.A.P.</creator><creatorcontrib>Ramírez, Orlando ; Pomareda, Florencia ; Olivares, Belén ; Huang, Ya-Lin ; Zavala, Gabriela ; Carrasco-Rojas, Javiera ; Álvarez, Simón ; Leiva-Sabadini, Camila ; Hidalgo, Valeria ; Romo, Pablo ; Sánchez, Matías ; Vargas, Ayleen ; Martínez, Jessica ; Aguayo, Sebastian ; Schuh, Christina M.A.P.</creatorcontrib><description>Aloe vera (AV) is a medicinal plant, most known for its beneficial effects on a variety of skin conditions. Its known active compounds include carbohydrates and flavonoids such as quercetin and kaempferol, among others. In the past decade, plant nanovesicles (NVs) have gained considerable interest as interkingdom communicators, presenting an opportunity for clinical standardization of natural products. In this study, we aimed to assess the potential of AVpNVs for the treatment of burn wounds.
AVpNVs were isolated and characterized regarding vesicle yield (nanoparticle tracking analysis) and structure (transmission electron microscopy and atomic force microscopy), as well as their protein content with proteomics. We assessed key characteristics for treating burn wounds in vitro, such as the anti-inflammatory potential in LPS-stimulated macrophages and keratinocytes, and the effect of AVpNVs on myofibroblast differentiation and contraction.
AVpNVs presented a homogenous NV population, vesicular shape, and NV-associated protein markers. AVpNVs significantly decreased the secretion of pro-inflammatory cytokines TNFα, IL-1β, and IL-6. Furthermore, AVpNVs inhibited myofibroblast differentiation and significantly decreased their contractile potential in collagen matrices. Observed effects were linked to proteins identified in the isolates through proteomics analysis.
AVpNVs displayed characteristics as an inflammatory modulator, while simultaneously diminishing myofibroblast differentiation and contraction. Novel strategies for burn wound treatment seek to decrease scarring on a cellular and molecular level in the early stages of wound healing, which makes AVpNVs a promising candidate for future plant-vesicle-based treatments.</description><identifier>ISSN: 0944-7113</identifier><identifier>EISSN: 1618-095X</identifier><identifier>DOI: 10.1016/j.phymed.2023.155108</identifier><language>eng</language><publisher>Elsevier GmbH</publisher><subject>Aloe vera ; anti-inflammatory activity ; atomic force microscopy ; collagen ; Interkingdom communication ; interleukin-6 ; kaempferol ; keratinocytes ; macrophages ; medicinal plants ; nanoparticles ; Nanotherapy ; Plant extracellular vesicles ; protein content ; proteomics ; quercetin ; secretion ; transmission electron microscopy</subject><ispartof>Phytomedicine (Stuttgart), 2024-01, Vol.122, p.155108-155108, Article 155108</ispartof><rights>2023 Elsevier GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-93e1961d99056ee32bdc0cd9dce6d993201c4c59695a68e1b7c6666fa4ef17093</citedby><cites>FETCH-LOGICAL-c372t-93e1961d99056ee32bdc0cd9dce6d993201c4c59695a68e1b7c6666fa4ef17093</cites><orcidid>0000-0002-5532-1130 ; 0000-0001-6240-6151 ; 0000-0002-0711-433X ; 0000-0001-6950-8433 ; 0000-0002-4745-9498 ; 0000-0002-3354-6742 ; 0000-0003-0900-1993 ; 0000-0002-7945-1714 ; 0009-0002-2512-3325 ; 0000-0001-9475-4513 ; 0009-0005-2235-7590</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.phymed.2023.155108$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids></links><search><creatorcontrib>Ramírez, Orlando</creatorcontrib><creatorcontrib>Pomareda, Florencia</creatorcontrib><creatorcontrib>Olivares, Belén</creatorcontrib><creatorcontrib>Huang, Ya-Lin</creatorcontrib><creatorcontrib>Zavala, Gabriela</creatorcontrib><creatorcontrib>Carrasco-Rojas, Javiera</creatorcontrib><creatorcontrib>Álvarez, Simón</creatorcontrib><creatorcontrib>Leiva-Sabadini, Camila</creatorcontrib><creatorcontrib>Hidalgo, Valeria</creatorcontrib><creatorcontrib>Romo, Pablo</creatorcontrib><creatorcontrib>Sánchez, Matías</creatorcontrib><creatorcontrib>Vargas, Ayleen</creatorcontrib><creatorcontrib>Martínez, Jessica</creatorcontrib><creatorcontrib>Aguayo, Sebastian</creatorcontrib><creatorcontrib>Schuh, Christina M.A.P.</creatorcontrib><title>Aloe vera peel-derived nanovesicles display anti-inflammatory properties and prevent myofibroblast differentiation</title><title>Phytomedicine (Stuttgart)</title><description>Aloe vera (AV) is a medicinal plant, most known for its beneficial effects on a variety of skin conditions. Its known active compounds include carbohydrates and flavonoids such as quercetin and kaempferol, among others. In the past decade, plant nanovesicles (NVs) have gained considerable interest as interkingdom communicators, presenting an opportunity for clinical standardization of natural products. In this study, we aimed to assess the potential of AVpNVs for the treatment of burn wounds.
AVpNVs were isolated and characterized regarding vesicle yield (nanoparticle tracking analysis) and structure (transmission electron microscopy and atomic force microscopy), as well as their protein content with proteomics. We assessed key characteristics for treating burn wounds in vitro, such as the anti-inflammatory potential in LPS-stimulated macrophages and keratinocytes, and the effect of AVpNVs on myofibroblast differentiation and contraction.
AVpNVs presented a homogenous NV population, vesicular shape, and NV-associated protein markers. AVpNVs significantly decreased the secretion of pro-inflammatory cytokines TNFα, IL-1β, and IL-6. Furthermore, AVpNVs inhibited myofibroblast differentiation and significantly decreased their contractile potential in collagen matrices. Observed effects were linked to proteins identified in the isolates through proteomics analysis.
AVpNVs displayed characteristics as an inflammatory modulator, while simultaneously diminishing myofibroblast differentiation and contraction. Novel strategies for burn wound treatment seek to decrease scarring on a cellular and molecular level in the early stages of wound healing, which makes AVpNVs a promising candidate for future plant-vesicle-based treatments.</description><subject>Aloe vera</subject><subject>anti-inflammatory activity</subject><subject>atomic force microscopy</subject><subject>collagen</subject><subject>Interkingdom communication</subject><subject>interleukin-6</subject><subject>kaempferol</subject><subject>keratinocytes</subject><subject>macrophages</subject><subject>medicinal plants</subject><subject>nanoparticles</subject><subject>Nanotherapy</subject><subject>Plant extracellular vesicles</subject><subject>protein content</subject><subject>proteomics</subject><subject>quercetin</subject><subject>secretion</subject><subject>transmission electron microscopy</subject><issn>0944-7113</issn><issn>1618-095X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFUctKBDEQDKLguvoHHuboZdb0vHMRFvEFC14UvIVs0oNZMsmYxIH5e7OMZ-1DN11UFd0UIddAN0ChuT1sxs95QLUpaFFuoK6BdidkBQ10OWX1xylZUVZVeQtQnpOLEA6UQsVauiJ-axxmE3qRjYgmV-j1hCqzwroJg5YGQ6Z0GI2YM2GjzrXtjRgGEZ2fs9G7EX3UiSSsSitOaGM2zK7Xe-_2RoSY5H2PPuFaRO3sJTnrhQl49TvX5P3x4e3-Od-9Pr3cb3e5LNsi5qxEYA0oxmjdIJbFXkkqFVMSmwSWBQVZyZo1rBZNh7BvZZOqFxX20FJWrsnN4puO_PrGEPmgg0RjhEX3HXgJdQVdW7PiX2rRtV3Bjj1Rq4UqvQvBY89HrwfhZw6UH9PgB76kwY9p8CWNJLtbZJg-njR6HqRGK1FpjzJy5fTfBj97LZfd</recordid><startdate>202401</startdate><enddate>202401</enddate><creator>Ramírez, Orlando</creator><creator>Pomareda, Florencia</creator><creator>Olivares, Belén</creator><creator>Huang, Ya-Lin</creator><creator>Zavala, Gabriela</creator><creator>Carrasco-Rojas, Javiera</creator><creator>Álvarez, Simón</creator><creator>Leiva-Sabadini, Camila</creator><creator>Hidalgo, Valeria</creator><creator>Romo, Pablo</creator><creator>Sánchez, Matías</creator><creator>Vargas, Ayleen</creator><creator>Martínez, Jessica</creator><creator>Aguayo, Sebastian</creator><creator>Schuh, Christina M.A.P.</creator><general>Elsevier GmbH</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0002-5532-1130</orcidid><orcidid>https://orcid.org/0000-0001-6240-6151</orcidid><orcidid>https://orcid.org/0000-0002-0711-433X</orcidid><orcidid>https://orcid.org/0000-0001-6950-8433</orcidid><orcidid>https://orcid.org/0000-0002-4745-9498</orcidid><orcidid>https://orcid.org/0000-0002-3354-6742</orcidid><orcidid>https://orcid.org/0000-0003-0900-1993</orcidid><orcidid>https://orcid.org/0000-0002-7945-1714</orcidid><orcidid>https://orcid.org/0009-0002-2512-3325</orcidid><orcidid>https://orcid.org/0000-0001-9475-4513</orcidid><orcidid>https://orcid.org/0009-0005-2235-7590</orcidid></search><sort><creationdate>202401</creationdate><title>Aloe vera peel-derived nanovesicles display anti-inflammatory properties and prevent myofibroblast differentiation</title><author>Ramírez, Orlando ; Pomareda, Florencia ; Olivares, Belén ; Huang, Ya-Lin ; Zavala, Gabriela ; Carrasco-Rojas, Javiera ; Álvarez, Simón ; Leiva-Sabadini, Camila ; Hidalgo, Valeria ; Romo, Pablo ; Sánchez, Matías ; Vargas, Ayleen ; Martínez, Jessica ; Aguayo, Sebastian ; Schuh, Christina M.A.P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-93e1961d99056ee32bdc0cd9dce6d993201c4c59695a68e1b7c6666fa4ef17093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Aloe vera</topic><topic>anti-inflammatory activity</topic><topic>atomic force microscopy</topic><topic>collagen</topic><topic>Interkingdom communication</topic><topic>interleukin-6</topic><topic>kaempferol</topic><topic>keratinocytes</topic><topic>macrophages</topic><topic>medicinal plants</topic><topic>nanoparticles</topic><topic>Nanotherapy</topic><topic>Plant extracellular vesicles</topic><topic>protein content</topic><topic>proteomics</topic><topic>quercetin</topic><topic>secretion</topic><topic>transmission electron microscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ramírez, Orlando</creatorcontrib><creatorcontrib>Pomareda, Florencia</creatorcontrib><creatorcontrib>Olivares, Belén</creatorcontrib><creatorcontrib>Huang, Ya-Lin</creatorcontrib><creatorcontrib>Zavala, Gabriela</creatorcontrib><creatorcontrib>Carrasco-Rojas, Javiera</creatorcontrib><creatorcontrib>Álvarez, Simón</creatorcontrib><creatorcontrib>Leiva-Sabadini, Camila</creatorcontrib><creatorcontrib>Hidalgo, Valeria</creatorcontrib><creatorcontrib>Romo, Pablo</creatorcontrib><creatorcontrib>Sánchez, Matías</creatorcontrib><creatorcontrib>Vargas, Ayleen</creatorcontrib><creatorcontrib>Martínez, Jessica</creatorcontrib><creatorcontrib>Aguayo, Sebastian</creatorcontrib><creatorcontrib>Schuh, Christina M.A.P.</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Phytomedicine (Stuttgart)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ramírez, Orlando</au><au>Pomareda, Florencia</au><au>Olivares, Belén</au><au>Huang, Ya-Lin</au><au>Zavala, Gabriela</au><au>Carrasco-Rojas, Javiera</au><au>Álvarez, Simón</au><au>Leiva-Sabadini, Camila</au><au>Hidalgo, Valeria</au><au>Romo, Pablo</au><au>Sánchez, Matías</au><au>Vargas, Ayleen</au><au>Martínez, Jessica</au><au>Aguayo, Sebastian</au><au>Schuh, Christina M.A.P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aloe vera peel-derived nanovesicles display anti-inflammatory properties and prevent myofibroblast differentiation</atitle><jtitle>Phytomedicine (Stuttgart)</jtitle><date>2024-01</date><risdate>2024</risdate><volume>122</volume><spage>155108</spage><epage>155108</epage><pages>155108-155108</pages><artnum>155108</artnum><issn>0944-7113</issn><eissn>1618-095X</eissn><abstract>Aloe vera (AV) is a medicinal plant, most known for its beneficial effects on a variety of skin conditions. Its known active compounds include carbohydrates and flavonoids such as quercetin and kaempferol, among others. In the past decade, plant nanovesicles (NVs) have gained considerable interest as interkingdom communicators, presenting an opportunity for clinical standardization of natural products. In this study, we aimed to assess the potential of AVpNVs for the treatment of burn wounds.
AVpNVs were isolated and characterized regarding vesicle yield (nanoparticle tracking analysis) and structure (transmission electron microscopy and atomic force microscopy), as well as their protein content with proteomics. We assessed key characteristics for treating burn wounds in vitro, such as the anti-inflammatory potential in LPS-stimulated macrophages and keratinocytes, and the effect of AVpNVs on myofibroblast differentiation and contraction.
AVpNVs presented a homogenous NV population, vesicular shape, and NV-associated protein markers. AVpNVs significantly decreased the secretion of pro-inflammatory cytokines TNFα, IL-1β, and IL-6. Furthermore, AVpNVs inhibited myofibroblast differentiation and significantly decreased their contractile potential in collagen matrices. Observed effects were linked to proteins identified in the isolates through proteomics analysis.
AVpNVs displayed characteristics as an inflammatory modulator, while simultaneously diminishing myofibroblast differentiation and contraction. Novel strategies for burn wound treatment seek to decrease scarring on a cellular and molecular level in the early stages of wound healing, which makes AVpNVs a promising candidate for future plant-vesicle-based treatments.</abstract><pub>Elsevier GmbH</pub><doi>10.1016/j.phymed.2023.155108</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-5532-1130</orcidid><orcidid>https://orcid.org/0000-0001-6240-6151</orcidid><orcidid>https://orcid.org/0000-0002-0711-433X</orcidid><orcidid>https://orcid.org/0000-0001-6950-8433</orcidid><orcidid>https://orcid.org/0000-0002-4745-9498</orcidid><orcidid>https://orcid.org/0000-0002-3354-6742</orcidid><orcidid>https://orcid.org/0000-0003-0900-1993</orcidid><orcidid>https://orcid.org/0000-0002-7945-1714</orcidid><orcidid>https://orcid.org/0009-0002-2512-3325</orcidid><orcidid>https://orcid.org/0000-0001-9475-4513</orcidid><orcidid>https://orcid.org/0009-0005-2235-7590</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0944-7113 |
ispartof | Phytomedicine (Stuttgart), 2024-01, Vol.122, p.155108-155108, Article 155108 |
issn | 0944-7113 1618-095X |
language | eng |
recordid | cdi_proquest_miscellaneous_3154187592 |
source | Elsevier ScienceDirect Journals |
subjects | Aloe vera anti-inflammatory activity atomic force microscopy collagen Interkingdom communication interleukin-6 kaempferol keratinocytes macrophages medicinal plants nanoparticles Nanotherapy Plant extracellular vesicles protein content proteomics quercetin secretion transmission electron microscopy |
title | Aloe vera peel-derived nanovesicles display anti-inflammatory properties and prevent myofibroblast differentiation |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-18T04%3A08%3A46IST&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=Aloe%20vera%20peel-derived%20nanovesicles%20display%20anti-inflammatory%20properties%20and%20prevent%20myofibroblast%20differentiation&rft.jtitle=Phytomedicine%20(Stuttgart)&rft.au=Ram%C3%ADrez,%20Orlando&rft.date=2024-01&rft.volume=122&rft.spage=155108&rft.epage=155108&rft.pages=155108-155108&rft.artnum=155108&rft.issn=0944-7113&rft.eissn=1618-095X&rft_id=info:doi/10.1016/j.phymed.2023.155108&rft_dat=%3Cproquest_cross%3E3154187592%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=2878292878&rft_id=info:pmid/&rft_els_id=S0944711323004683&rfr_iscdi=true |