Small extracellular vesicles derived from dermal fibroblasts promote fibroblast activity and skin development through carrying miR-218 and ITGBL1

Abstract Skin thickness is closely related to the appearance of human skin, such as sagging and wrinkling, which primarily depends on the level of collagen I synthesized by dermal fibroblasts (DFs). Small extracellular vesicles (SEVs), especially those derived from human DFs (HDFs), are crucial orch...

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Published in:Journal of Nanobiotechnology
Main Authors: Qin Zou, Mei Zhang, Rong Yuan, Yifei Wang, Zhengyin Gong, Rui Shi, Yujing Li, Kaixin Fei, Chenggang Luo, Ying Xiong, Ting Zheng, Li Zhu, Guoqing Tang, Mingzhou Li, Xuewei Li, Yanzhi Jiang
Format: Article
Language:English
Published: BMC 2022-06-01
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Online Access:https://doi.org/10.1186/s12951-022-01499-2
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author Qin Zou
Mei Zhang
Rong Yuan
Yifei Wang
Zhengyin Gong
Rui Shi
Yujing Li
Kaixin Fei
Chenggang Luo
Ying Xiong
Ting Zheng
Li Zhu
Guoqing Tang
Mingzhou Li
Xuewei Li
Yanzhi Jiang
author_facet Qin Zou
Mei Zhang
Rong Yuan
Yifei Wang
Zhengyin Gong
Rui Shi
Yujing Li
Kaixin Fei
Chenggang Luo
Ying Xiong
Ting Zheng
Li Zhu
Guoqing Tang
Mingzhou Li
Xuewei Li
Yanzhi Jiang
author_sort Qin Zou
collection DOAJ
container_title Journal of Nanobiotechnology
description Abstract Skin thickness is closely related to the appearance of human skin, such as sagging and wrinkling, which primarily depends on the level of collagen I synthesized by dermal fibroblasts (DFs). Small extracellular vesicles (SEVs), especially those derived from human DFs (HDFs), are crucial orchestrators in shaping physiological and pathological development of skin. However, the limited supply of human skin prevents the production of a large amount of HDFs-SEVs, and pig skin is used as a model of human skin. In this study, SEVs derived from DFs of Chenghua pigs (CH-SEVs), considered to have superior skin thickness, and Large White pigs (LW-SEVs) were collected to compare their effects on DFs and skin tissue. Our results showed that, compared with LW-SEVs, CH-SEVs more effectively promoted fibroblast proliferation, migration, collagen synthesis and contraction; in addition, in mouse model injected with both SEVs, compared with LW-SEVs, CH-SEVs increased the skin thickness and collagen I content more effectively. Some differentially expressed miRNAs and proteins were found between CH-SEVs and LW-SEVs by small RNA-seq and LC–MS/MS analysis. Interestingly, we identified that CH-SEVs were enriched in miRNA-218 and ITGBL1 protein, which played important roles in promoting fibroblast activity via activation of the downstream TGFβ1-SMAD2/3 pathway in vitro. Furthermore, overexpression of miRNA-218 and ITGBL1 protein increased the thickness and collagen I content of mouse skin in vivo. These results indicate that CH-SEVs can effectively stimulate fibroblast activity and promote skin development and thus have the potential to protect against and repair skin damage. Graphical Abstract
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spelling doaj-art-e6ac2900a4264da6820e6aeca64e89732025-08-19T20:51:08ZengBMCJournal of Nanobiotechnology1477-31552022-06-0120111610.1186/s12951-022-01499-2Small extracellular vesicles derived from dermal fibroblasts promote fibroblast activity and skin development through carrying miR-218 and ITGBL1Qin Zou0Mei Zhang1Rong Yuan2Yifei Wang3Zhengyin Gong4Rui Shi5Yujing Li6Kaixin Fei7Chenggang Luo8Ying Xiong9Ting Zheng10Li Zhu11Guoqing Tang12Mingzhou Li13Xuewei Li14Yanzhi Jiang15Department of Zoology, College of Life Science, Sichuan Agricultural UniversityDepartment of Zoology, College of Life Science, Sichuan Agricultural UniversityChengdu Livestock and Poultry Genetic Resources Protection CenterDepartment of Zoology, College of Life Science, Sichuan Agricultural UniversityDepartment of Zoology, College of Life Science, Sichuan Agricultural UniversityDepartment of Zoology, College of Life Science, Sichuan Agricultural UniversityDepartment of Zoology, College of Life Science, Sichuan Agricultural UniversityDepartment of Zoology, College of Life Science, Sichuan Agricultural UniversityChengdu Livestock and Poultry Genetic Resources Protection CenterDepartment of Zoology, College of Life Science, Sichuan Agricultural UniversityDepartment of Zoology, College of Life Science, Sichuan Agricultural UniversityInstitute of Animal Genetics and Breeding, College of Animal Science and Technology, Sichuan Agricultural UniversityInstitute of Animal Genetics and Breeding, College of Animal Science and Technology, Sichuan Agricultural UniversityInstitute of Animal Genetics and Breeding, College of Animal Science and Technology, Sichuan Agricultural UniversityInstitute of Animal Genetics and Breeding, College of Animal Science and Technology, Sichuan Agricultural UniversityDepartment of Zoology, College of Life Science, Sichuan Agricultural UniversityAbstract Skin thickness is closely related to the appearance of human skin, such as sagging and wrinkling, which primarily depends on the level of collagen I synthesized by dermal fibroblasts (DFs). Small extracellular vesicles (SEVs), especially those derived from human DFs (HDFs), are crucial orchestrators in shaping physiological and pathological development of skin. However, the limited supply of human skin prevents the production of a large amount of HDFs-SEVs, and pig skin is used as a model of human skin. In this study, SEVs derived from DFs of Chenghua pigs (CH-SEVs), considered to have superior skin thickness, and Large White pigs (LW-SEVs) were collected to compare their effects on DFs and skin tissue. Our results showed that, compared with LW-SEVs, CH-SEVs more effectively promoted fibroblast proliferation, migration, collagen synthesis and contraction; in addition, in mouse model injected with both SEVs, compared with LW-SEVs, CH-SEVs increased the skin thickness and collagen I content more effectively. Some differentially expressed miRNAs and proteins were found between CH-SEVs and LW-SEVs by small RNA-seq and LC–MS/MS analysis. Interestingly, we identified that CH-SEVs were enriched in miRNA-218 and ITGBL1 protein, which played important roles in promoting fibroblast activity via activation of the downstream TGFβ1-SMAD2/3 pathway in vitro. Furthermore, overexpression of miRNA-218 and ITGBL1 protein increased the thickness and collagen I content of mouse skin in vivo. These results indicate that CH-SEVs can effectively stimulate fibroblast activity and promote skin development and thus have the potential to protect against and repair skin damage. Graphical Abstracthttps://doi.org/10.1186/s12951-022-01499-2Dermal fibroblastsSmall extracellular vesiclesFibroblast activitySkin developmentmiR-218ITGBL1
spellingShingle Qin Zou
Mei Zhang
Rong Yuan
Yifei Wang
Zhengyin Gong
Rui Shi
Yujing Li
Kaixin Fei
Chenggang Luo
Ying Xiong
Ting Zheng
Li Zhu
Guoqing Tang
Mingzhou Li
Xuewei Li
Yanzhi Jiang
Small extracellular vesicles derived from dermal fibroblasts promote fibroblast activity and skin development through carrying miR-218 and ITGBL1
Dermal fibroblasts
Small extracellular vesicles
Fibroblast activity
Skin development
miR-218
ITGBL1
title Small extracellular vesicles derived from dermal fibroblasts promote fibroblast activity and skin development through carrying miR-218 and ITGBL1
title_full Small extracellular vesicles derived from dermal fibroblasts promote fibroblast activity and skin development through carrying miR-218 and ITGBL1
title_fullStr Small extracellular vesicles derived from dermal fibroblasts promote fibroblast activity and skin development through carrying miR-218 and ITGBL1
title_full_unstemmed Small extracellular vesicles derived from dermal fibroblasts promote fibroblast activity and skin development through carrying miR-218 and ITGBL1
title_short Small extracellular vesicles derived from dermal fibroblasts promote fibroblast activity and skin development through carrying miR-218 and ITGBL1
title_sort small extracellular vesicles derived from dermal fibroblasts promote fibroblast activity and skin development through carrying mir 218 and itgbl1
topic Dermal fibroblasts
Small extracellular vesicles
Fibroblast activity
Skin development
miR-218
ITGBL1
url https://doi.org/10.1186/s12951-022-01499-2
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