Exosomes Derived from Fisetin-Treated Keratinocytes Mediate Hair Growth Promotion

Enhanced telomerase reverse transcriptase (TERT) levels in dermal keratinocytes can serve as a novel target for hair growth promotion. Previously, we identified fisetin using a system for screening food components that can activate the TERT promoter in HaCaT cells (keratinocytes). In the present stu...

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Main Authors: Mizuki Ogawa, Miyako Udono, Kiichiro Teruya, Norihisa Uehara, Yoshinori Katakura
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Nutrients
Subjects:
Online Access:https://www.mdpi.com/2072-6643/13/6/2087
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author Mizuki Ogawa
Miyako Udono
Kiichiro Teruya
Norihisa Uehara
Yoshinori Katakura
author_facet Mizuki Ogawa
Miyako Udono
Kiichiro Teruya
Norihisa Uehara
Yoshinori Katakura
author_sort Mizuki Ogawa
collection DOAJ
description Enhanced telomerase reverse transcriptase (TERT) levels in dermal keratinocytes can serve as a novel target for hair growth promotion. Previously, we identified fisetin using a system for screening food components that can activate the TERT promoter in HaCaT cells (keratinocytes). In the present study, we aimed to clarify the molecular basis of fisetin-induced hair growth promotion in mice. To this end, the dorsal skin of mice was treated with fisetin, and hair growth was evaluated 12 days after treatment. Histochemical analyses of fisetin-treated skin samples and HaCaT cells were performed to observe the effects of fisetin. The results showed that fisetin activated HaCaT cells by regulating the expression of various genes related to epidermogenesis, cell proliferation, hair follicle regulation, and hair cycle regulation. In addition, fisetin induced the secretion of exosomes from HaCaT cells, which activated β-catenin and mitochondria in hair follicle stem cells (HFSCs) and induced their proliferation. Moreover, these results revealed the existence of exosomes as the molecular basis of keratinocyte-HFSC interaction and showed that fisetin, along with its effects on keratinocytes, caused exosome secretion, thereby activating HFSCs. This is the first study to show that keratinocyte-derived exosomes can activate HFSCs and consequently induce hair growth.
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spelling doaj.art-2bac127e02f948f0b8d56e1ebbc84fdc2023-11-22T00:39:51ZengMDPI AGNutrients2072-66432021-06-01136208710.3390/nu13062087Exosomes Derived from Fisetin-Treated Keratinocytes Mediate Hair Growth PromotionMizuki Ogawa0Miyako Udono1Kiichiro Teruya2Norihisa Uehara3Yoshinori Katakura4Graduate School of Bioresources and Bioenvironmental Sciences, Kyushu University, Fukuoka 819-0395, JapanFaculty of Agriculture, Kyushu University, Fukuoka 819-0395, JapanGraduate School of Bioresources and Bioenvironmental Sciences, Kyushu University, Fukuoka 819-0395, JapanDepartment of Molecular Cell Biology and Oral Anatomy, Faculty of Dental Science, Kyushu University, Fukuoka 812-8582, JapanGraduate School of Bioresources and Bioenvironmental Sciences, Kyushu University, Fukuoka 819-0395, JapanEnhanced telomerase reverse transcriptase (TERT) levels in dermal keratinocytes can serve as a novel target for hair growth promotion. Previously, we identified fisetin using a system for screening food components that can activate the TERT promoter in HaCaT cells (keratinocytes). In the present study, we aimed to clarify the molecular basis of fisetin-induced hair growth promotion in mice. To this end, the dorsal skin of mice was treated with fisetin, and hair growth was evaluated 12 days after treatment. Histochemical analyses of fisetin-treated skin samples and HaCaT cells were performed to observe the effects of fisetin. The results showed that fisetin activated HaCaT cells by regulating the expression of various genes related to epidermogenesis, cell proliferation, hair follicle regulation, and hair cycle regulation. In addition, fisetin induced the secretion of exosomes from HaCaT cells, which activated β-catenin and mitochondria in hair follicle stem cells (HFSCs) and induced their proliferation. Moreover, these results revealed the existence of exosomes as the molecular basis of keratinocyte-HFSC interaction and showed that fisetin, along with its effects on keratinocytes, caused exosome secretion, thereby activating HFSCs. This is the first study to show that keratinocyte-derived exosomes can activate HFSCs and consequently induce hair growth.https://www.mdpi.com/2072-6643/13/6/2087telomerase reverse transcriptasekeratinocyte–hair follicle stem cell interactionexosomestelogen–anagen transitionhair cycle regulation
spellingShingle Mizuki Ogawa
Miyako Udono
Kiichiro Teruya
Norihisa Uehara
Yoshinori Katakura
Exosomes Derived from Fisetin-Treated Keratinocytes Mediate Hair Growth Promotion
Nutrients
telomerase reverse transcriptase
keratinocyte–hair follicle stem cell interaction
exosomes
telogen–anagen transition
hair cycle regulation
title Exosomes Derived from Fisetin-Treated Keratinocytes Mediate Hair Growth Promotion
title_full Exosomes Derived from Fisetin-Treated Keratinocytes Mediate Hair Growth Promotion
title_fullStr Exosomes Derived from Fisetin-Treated Keratinocytes Mediate Hair Growth Promotion
title_full_unstemmed Exosomes Derived from Fisetin-Treated Keratinocytes Mediate Hair Growth Promotion
title_short Exosomes Derived from Fisetin-Treated Keratinocytes Mediate Hair Growth Promotion
title_sort exosomes derived from fisetin treated keratinocytes mediate hair growth promotion
topic telomerase reverse transcriptase
keratinocyte–hair follicle stem cell interaction
exosomes
telogen–anagen transition
hair cycle regulation
url https://www.mdpi.com/2072-6643/13/6/2087
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AT norihisauehara exosomesderivedfromfisetintreatedkeratinocytesmediatehairgrowthpromotion
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