Extracellular vesicles derived from MSCs activates dermal papilla cell in vitro and promotes hair follicle conversion from telogen to anagen in mice

Hair loss is a common medical problem. In this study, we investigated the proliferation, migration, and growth factor expression of human dermal papilla (DP) cells in the presence or absence of treatment with mesenchymal stem cell extracellular vesicles (MSC-EVs). In addition, we tested the efficacy...

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Published inScientific reports Vol. 7; no. 1; pp. 15560 - 12
Main Authors Rajendran, Ramya Lakshmi, Gangadaran, Prakash, Bak, Soon Sun, Oh, Ji Min, Kalimuthu, Senthilkumar, Lee, Ho Won, Baek, Se Hwan, Zhu, Liya, Sung, Young Kwan, Jeong, Shin Young, Lee, Sang-Woo, Lee, Jaetae, Ahn, Byeong-Cheol
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LanguageEnglish
Published London Nature Publishing Group UK 14.11.2017
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Abstract Hair loss is a common medical problem. In this study, we investigated the proliferation, migration, and growth factor expression of human dermal papilla (DP) cells in the presence or absence of treatment with mesenchymal stem cell extracellular vesicles (MSC-EVs). In addition, we tested the efficacy of MSC-EV treatment on hair growth in an animal model. MSC-EV treatment increased DP cell proliferation and migration, and elevated the levels of Bcl-2, phosphorylated Akt and ERK. In addition; DP cells treated with MSC-EVs displayed increased expression and secretion of VEGF and IGF-1. Intradermal injection of MSC-EVs into C57BL/6 mice promoted the conversion from telogen to anagen and increased expression of wnt3a, wnt5a and versican was demonstrated. The first time our results suggest that MSC-EVs have a potential to activate DP cells, prolonged survival, induce growth factor activation in vitro , and promotes hair growth in vivo .
AbstractList Hair loss is a common medical problem. In this study, we investigated the proliferation, migration, and growth factor expression of human dermal papilla (DP) cells in the presence or absence of treatment with mesenchymal stem cell extracellular vesicles (MSC-EVs). In addition, we tested the efficacy of MSC-EV treatment on hair growth in an animal model. MSC-EV treatment increased DP cell proliferation and migration, and elevated the levels of Bcl-2, phosphorylated Akt and ERK. In addition; DP cells treated with MSC-EVs displayed increased expression and secretion of VEGF and IGF-1. Intradermal injection of MSC-EVs into C57BL/6 mice promoted the conversion from telogen to anagen and increased expression of wnt3a, wnt5a and versican was demonstrated. The first time our results suggest that MSC-EVs have a potential to activate DP cells, prolonged survival, induce growth factor activation in vitro, and promotes hair growth in vivo.
Hair loss is a common medical problem. In this study, we investigated the proliferation, migration, and growth factor expression of human dermal papilla (DP) cells in the presence or absence of treatment with mesenchymal stem cell extracellular vesicles (MSC-EVs). In addition, we tested the efficacy of MSC-EV treatment on hair growth in an animal model. MSC-EV treatment increased DP cell proliferation and migration, and elevated the levels of Bcl-2, phosphorylated Akt and ERK. In addition; DP cells treated with MSC-EVs displayed increased expression and secretion of VEGF and IGF-1. Intradermal injection of MSC-EVs into C57BL/6 mice promoted the conversion from telogen to anagen and increased expression of wnt3a, wnt5a and versican was demonstrated. The first time our results suggest that MSC-EVs have a potential to activate DP cells, prolonged survival, induce growth factor activation in vitro , and promotes hair growth in vivo .
Abstract Hair loss is a common medical problem. In this study, we investigated the proliferation, migration, and growth factor expression of human dermal papilla (DP) cells in the presence or absence of treatment with mesenchymal stem cell extracellular vesicles (MSC-EVs). In addition, we tested the efficacy of MSC-EV treatment on hair growth in an animal model. MSC-EV treatment increased DP cell proliferation and migration, and elevated the levels of Bcl-2, phosphorylated Akt and ERK. In addition; DP cells treated with MSC-EVs displayed increased expression and secretion of VEGF and IGF-1. Intradermal injection of MSC-EVs into C57BL/6 mice promoted the conversion from telogen to anagen and increased expression of wnt3a, wnt5a and versican was demonstrated. The first time our results suggest that MSC-EVs have a potential to activate DP cells, prolonged survival, induce growth factor activation in vitro , and promotes hair growth in vivo .
ArticleNumber 15560
Author Baek, Se Hwan
Ahn, Byeong-Cheol
Lee, Sang-Woo
Lee, Jaetae
Rajendran, Ramya Lakshmi
Oh, Ji Min
Kalimuthu, Senthilkumar
Jeong, Shin Young
Sung, Young Kwan
Gangadaran, Prakash
Zhu, Liya
Bak, Soon Sun
Lee, Ho Won
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  surname: Ahn
  fullname: Ahn, Byeong-Cheol
  email: abc2000@knu.ac.kr
  organization: Department of Nuclear Medicine, Kyungpook National University School of Medicine/Hospital
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Snippet Hair loss is a common medical problem. In this study, we investigated the proliferation, migration, and growth factor expression of human dermal papilla (DP)...
Abstract Hair loss is a common medical problem. In this study, we investigated the proliferation, migration, and growth factor expression of human dermal...
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proquest
crossref
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springer
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StartPage 15560
SubjectTerms 101/28
13
13/100
14
38
45/77
631/136/532/2074
631/532/2074
64/60
96/1
96/21
AKT protein
Bcl-2 protein
Cell proliferation
Extracellular vesicles
Growth factors
Hair
Hair loss
Humanities and Social Sciences
Insulin-like growth factor I
Mesenchyme
multidisciplinary
Science
Science (multidisciplinary)
Secretion
Skin
Stem cells
Vascular endothelial growth factor
Versican
Wnt protein
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Title Extracellular vesicles derived from MSCs activates dermal papilla cell in vitro and promotes hair follicle conversion from telogen to anagen in mice
URI https://link.springer.com/article/10.1038/s41598-017-15505-3
https://www.ncbi.nlm.nih.gov/pubmed/29138430
https://www.proquest.com/docview/1964065924
https://search.proquest.com/docview/1964701002
https://pubmed.ncbi.nlm.nih.gov/PMC5686117
Volume 7
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