Cargando…

Transcriptomic and in vivo approaches introduced human iPSC-derived microvesicles for skin rejuvenation

The skin undergoes the formation of fine lines and wrinkles through the aging process; also, burns, trauma, and other similar circumstances give rise to various forms of skin ulcers. Induced pluripotent stem cells (iPSCs) have become promising candidates for skin healing and rejuvenation due to not...

Descripción completa

Detalles Bibliográficos
Autores principales: Bakhshandeh, Behnaz, Jahanafrooz, Zohreh, Allahdadi, Shiva, Daryani, Shiva, Dehghani, Zahra, Sadeghi, Mahya, Pedram, Mir Sepehr, Dehghan, Mohammad Mehdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10282097/
https://www.ncbi.nlm.nih.gov/pubmed/37339980
http://dx.doi.org/10.1038/s41598-023-36162-9
_version_ 1785061124246339584
author Bakhshandeh, Behnaz
Jahanafrooz, Zohreh
Allahdadi, Shiva
Daryani, Shiva
Dehghani, Zahra
Sadeghi, Mahya
Pedram, Mir Sepehr
Dehghan, Mohammad Mehdi
author_facet Bakhshandeh, Behnaz
Jahanafrooz, Zohreh
Allahdadi, Shiva
Daryani, Shiva
Dehghani, Zahra
Sadeghi, Mahya
Pedram, Mir Sepehr
Dehghan, Mohammad Mehdi
author_sort Bakhshandeh, Behnaz
collection PubMed
description The skin undergoes the formation of fine lines and wrinkles through the aging process; also, burns, trauma, and other similar circumstances give rise to various forms of skin ulcers. Induced pluripotent stem cells (iPSCs) have become promising candidates for skin healing and rejuvenation due to not stimulating inflammatory responses, low probability of immune rejection, high metabolic activity, good large-scale production capacity and potentials for personalized medicine. iPSCs can secrete microvesicles (MVs) containing RNA and proteins responsible for the normal repairing process of the skin. This study aimed to evaluate the possibility, safety and effectiveness of applying iPSCs-derived MVs for skin tissue engineering and rejuvenation applications. The possibility was assessed using the evaluation of the mRNA content of iPSC-derived MVs and the behavior of fibroblasts after MV treatment. Investigating the effect of microvesicle on stemness potential of mesenchymal stem cells was performed for safety concerns. In vivo evaluation of MVs was done in order to investigate related immune response, re-epithelialization and blood vessel formation to measure effectiveness. Shedding MVs were round in shape distributed in the range from 100 to 1000 nm in diameter and positive for AQP3, COL2A, FGF2, ITGB, and SEPTIN4 mRNAs. After treating dermal fibroblasts with iPSC-derived MVs, the expressions of collagens Iα1 and III transcripts (as the main fibrous extracellular matrix (ECM) proteins) were upregulated. Meanwhile, the survival and proliferation of MV treated fibroblasts did not change significantly. Evaluation of stemness markers in MV treated MSCs showed negligible alteration. In line with in vitro results, histomorphometry and histopathology findings also confirmed the helpful effect of MVs in skin regeneration in the rat burn wound models. Conducting more investigations on hiPSCs-derived MVs may lead to produce more efficient and safer biopharmaceutics for skin regeneration in the pharmaceutical market.
format Online
Article
Text
id pubmed-10282097
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-102820972023-06-22 Transcriptomic and in vivo approaches introduced human iPSC-derived microvesicles for skin rejuvenation Bakhshandeh, Behnaz Jahanafrooz, Zohreh Allahdadi, Shiva Daryani, Shiva Dehghani, Zahra Sadeghi, Mahya Pedram, Mir Sepehr Dehghan, Mohammad Mehdi Sci Rep Article The skin undergoes the formation of fine lines and wrinkles through the aging process; also, burns, trauma, and other similar circumstances give rise to various forms of skin ulcers. Induced pluripotent stem cells (iPSCs) have become promising candidates for skin healing and rejuvenation due to not stimulating inflammatory responses, low probability of immune rejection, high metabolic activity, good large-scale production capacity and potentials for personalized medicine. iPSCs can secrete microvesicles (MVs) containing RNA and proteins responsible for the normal repairing process of the skin. This study aimed to evaluate the possibility, safety and effectiveness of applying iPSCs-derived MVs for skin tissue engineering and rejuvenation applications. The possibility was assessed using the evaluation of the mRNA content of iPSC-derived MVs and the behavior of fibroblasts after MV treatment. Investigating the effect of microvesicle on stemness potential of mesenchymal stem cells was performed for safety concerns. In vivo evaluation of MVs was done in order to investigate related immune response, re-epithelialization and blood vessel formation to measure effectiveness. Shedding MVs were round in shape distributed in the range from 100 to 1000 nm in diameter and positive for AQP3, COL2A, FGF2, ITGB, and SEPTIN4 mRNAs. After treating dermal fibroblasts with iPSC-derived MVs, the expressions of collagens Iα1 and III transcripts (as the main fibrous extracellular matrix (ECM) proteins) were upregulated. Meanwhile, the survival and proliferation of MV treated fibroblasts did not change significantly. Evaluation of stemness markers in MV treated MSCs showed negligible alteration. In line with in vitro results, histomorphometry and histopathology findings also confirmed the helpful effect of MVs in skin regeneration in the rat burn wound models. Conducting more investigations on hiPSCs-derived MVs may lead to produce more efficient and safer biopharmaceutics for skin regeneration in the pharmaceutical market. Nature Publishing Group UK 2023-06-20 /pmc/articles/PMC10282097/ /pubmed/37339980 http://dx.doi.org/10.1038/s41598-023-36162-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bakhshandeh, Behnaz
Jahanafrooz, Zohreh
Allahdadi, Shiva
Daryani, Shiva
Dehghani, Zahra
Sadeghi, Mahya
Pedram, Mir Sepehr
Dehghan, Mohammad Mehdi
Transcriptomic and in vivo approaches introduced human iPSC-derived microvesicles for skin rejuvenation
title Transcriptomic and in vivo approaches introduced human iPSC-derived microvesicles for skin rejuvenation
title_full Transcriptomic and in vivo approaches introduced human iPSC-derived microvesicles for skin rejuvenation
title_fullStr Transcriptomic and in vivo approaches introduced human iPSC-derived microvesicles for skin rejuvenation
title_full_unstemmed Transcriptomic and in vivo approaches introduced human iPSC-derived microvesicles for skin rejuvenation
title_short Transcriptomic and in vivo approaches introduced human iPSC-derived microvesicles for skin rejuvenation
title_sort transcriptomic and in vivo approaches introduced human ipsc-derived microvesicles for skin rejuvenation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10282097/
https://www.ncbi.nlm.nih.gov/pubmed/37339980
http://dx.doi.org/10.1038/s41598-023-36162-9
work_keys_str_mv AT bakhshandehbehnaz transcriptomicandinvivoapproachesintroducedhumanipscderivedmicrovesiclesforskinrejuvenation
AT jahanafroozzohreh transcriptomicandinvivoapproachesintroducedhumanipscderivedmicrovesiclesforskinrejuvenation
AT allahdadishiva transcriptomicandinvivoapproachesintroducedhumanipscderivedmicrovesiclesforskinrejuvenation
AT daryanishiva transcriptomicandinvivoapproachesintroducedhumanipscderivedmicrovesiclesforskinrejuvenation
AT dehghanizahra transcriptomicandinvivoapproachesintroducedhumanipscderivedmicrovesiclesforskinrejuvenation
AT sadeghimahya transcriptomicandinvivoapproachesintroducedhumanipscderivedmicrovesiclesforskinrejuvenation
AT pedrammirsepehr transcriptomicandinvivoapproachesintroducedhumanipscderivedmicrovesiclesforskinrejuvenation
AT dehghanmohammadmehdi transcriptomicandinvivoapproachesintroducedhumanipscderivedmicrovesiclesforskinrejuvenation