Visible red light enhances physiological anagen entry in vivo and has direct and indirect stimulative effects in vitro

Background and Objectives Hair follicles are located at the interface of the external and internal environments and their cycling has been shown to be regulated by intra‐ and extra‐follicular factors. The aim of this study is to examine whether or how hair follicles respond to visible light. Study D...

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Published inLasers in surgery and medicine Vol. 47; no. 1; pp. 50 - 59
Main Authors Sheen, Yi-Shuan, Fan, Sabrina Mai-Yi, Chan, Chih-Chieh, Wu, Yueh-Feng, Jee, Shiou-Hwa, Lin, Sung-Jan
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.01.2015
Wiley Subscription Services, Inc
Subjects
Animals
Biomarkers - metabolism
Cell Proliferation - radiation effects
dermal papilla cells
Dermis - metabolism
Dermis - radiation effects
Female
FGF7
Fibroblast Growth Factor 7 - metabolism
Hair - growth & development
Hair - radiation effects
hair cycle
Hair Follicle - physiology
Hair Follicle - radiation effects
In Vitro Techniques
Keratinocytes - metabolism
Keratinocytes - radiation effects
Light
Mice
Mice, Inbred C57BL
outer root sheath keratinocytes
Random Allocation
outer root sheath keratinocytes
FGF7
hair cycle
dermal papilla cells
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Abstract Background and Objectives Hair follicles are located at the interface of the external and internal environments and their cycling has been shown to be regulated by intra‐ and extra‐follicular factors. The aim of this study is to examine whether or how hair follicles respond to visible light. Study Design/Materials and Methods We examined the effect of 3 mW red (630 nm, 1 J/cm2), 2 mW green (522 nm, 1 J/cm2), and 2 mW blue light (463 nm, 1 J/cm2) on telogen in mice for 3 weeks. The photobiologic effects of red light on cell proliferation of outer root sheath keratinocytes and dermal papilla cells were studied in vitro. Results We found that red light accelerated anagen entry faster than green and blue light in mice. Red light irradiation stimulated the proliferation of both outer root sheath keratinocytes and dermal papilla cells in a dose‐dependent manner by promoting cell cycle progression. This stimulative effect was mediated via extracellular signal‐regulated kinase phosphorylation in both cells. In a co‐culture condition, dermal papilla cells irradiated by red light further enhanced keratinocyte proliferation, suggesting enhanced epithelial‐mesenchymal interaction. In search for factors that mediated this paracrine effect, we found fibroblast growth factor 7 was upregulated in both mRNA and protein levels. The stimulative paracrine effect on keratinocytes was significantly inhibited by neutralizing antibody against fibroblast growth factor 7. Conclusions These results suggest that hair follicles respond to visible light in vivo. Red light may promote physiological telogen to anagen transition by directly stimulating outer root sheath keratinocytes and indirectly by enhancing epithelial‐mesenchymal interaction in vitro. Lasers Surg. Med. 47:50–59, 2015. © 2014 Wiley Periodicals, Inc.
AbstractList Hair follicles are located at the interface of the external and internal environments and their cycling has been shown to be regulated by intra- and extra-follicular factors. The aim of this study is to examine whether or how hair follicles respond to visible light. We examined the effect of 3 mW red (630 nm, 1 J/cm(2)), 2 mW green (522 nm, 1 J/cm(2)), and 2 mW blue light (463 nm, 1 J/cm(2)) on telogen in mice for 3 weeks. The photobiologic effects of red light on cell proliferation of outer root sheath keratinocytes and dermal papilla cells were studied in vitro. We found that red light accelerated anagen entry faster than green and blue light in mice. Red light irradiation stimulated the proliferation of both outer root sheath keratinocytes and dermal papilla cells in a dose-dependent manner by promoting cell cycle progression. This stimulative effect was mediated via extracellular signal-regulated kinase phosphorylation in both cells. In a co-culture condition, dermal papilla cells irradiated by red light further enhanced keratinocyte proliferation, suggesting enhanced epithelial-mesenchymal interaction. In search for factors that mediated this paracrine effect, we found fibroblast growth factor 7 was upregulated in both mRNA and protein levels. The stimulative paracrine effect on keratinocytes was significantly inhibited by neutralizing antibody against fibroblast growth factor 7. These results suggest that hair follicles respond to visible light in vivo. Red light may promote physiological telogen to anagen transition by directly stimulating outer root sheath keratinocytes and indirectly by enhancing epithelial-mesenchymal interaction in vitro.
Background and Objectives Hair follicles are located at the interface of the external and internal environments and their cycling has been shown to be regulated by intra- and extra-follicular factors. The aim of this study is to examine whether or how hair follicles respond to visible light. Study Design/Materials and Methods We examined the effect of 3mW red (630nm, 1J/cm2), 2mW green (522nm, 1J/cm2), and 2mW blue light (463nm, 1J/cm2) on telogen in mice for 3 weeks. The photobiologic effects of red light on cell proliferation of outer root sheath keratinocytes and dermal papilla cells were studied in vitro. Results We found that red light accelerated anagen entry faster than green and blue light in mice. Red light irradiation stimulated the proliferation of both outer root sheath keratinocytes and dermal papilla cells in a dose-dependent manner by promoting cell cycle progression. This stimulative effect was mediated via extracellular signal-regulated kinase phosphorylation in both cells. In a co-culture condition, dermal papilla cells irradiated by red light further enhanced keratinocyte proliferation, suggesting enhanced epithelial-mesenchymal interaction. In search for factors that mediated this paracrine effect, we found fibroblast growth factor 7 was upregulated in both mRNA and protein levels. The stimulative paracrine effect on keratinocytes was significantly inhibited by neutralizing antibody against fibroblast growth factor 7. Conclusions These results suggest that hair follicles respond to visible light in vivo. Red light may promote physiological telogen to anagen transition by directly stimulating outer root sheath keratinocytes and indirectly by enhancing epithelial-mesenchymal interaction in vitro. Lasers Surg. Med. 47:50-59, 2015. © 2014 Wiley Periodicals, Inc.
BACKGROUND AND OBJECTIVESHair follicles are located at the interface of the external and internal environments and their cycling has been shown to be regulated by intra- and extra-follicular factors. The aim of this study is to examine whether or how hair follicles respond to visible light.STUDY DESIGN/MATERIALS AND METHODSWe examined the effect of 3 mW red (630 nm, 1 J/cm(2)), 2 mW green (522 nm, 1 J/cm(2)), and 2 mW blue light (463 nm, 1 J/cm(2)) on telogen in mice for 3 weeks. The photobiologic effects of red light on cell proliferation of outer root sheath keratinocytes and dermal papilla cells were studied in vitro.RESULTSWe found that red light accelerated anagen entry faster than green and blue light in mice. Red light irradiation stimulated the proliferation of both outer root sheath keratinocytes and dermal papilla cells in a dose-dependent manner by promoting cell cycle progression. This stimulative effect was mediated via extracellular signal-regulated kinase phosphorylation in both cells. In a co-culture condition, dermal papilla cells irradiated by red light further enhanced keratinocyte proliferation, suggesting enhanced epithelial-mesenchymal interaction. In search for factors that mediated this paracrine effect, we found fibroblast growth factor 7 was upregulated in both mRNA and protein levels. The stimulative paracrine effect on keratinocytes was significantly inhibited by neutralizing antibody against fibroblast growth factor 7.CONCLUSIONSThese results suggest that hair follicles respond to visible light in vivo. Red light may promote physiological telogen to anagen transition by directly stimulating outer root sheath keratinocytes and indirectly by enhancing epithelial-mesenchymal interaction in vitro.
Background and Objectives Hair follicles are located at the interface of the external and internal environments and their cycling has been shown to be regulated by intra- and extra-follicular factors. The aim of this study is to examine whether or how hair follicles respond to visible light. Study Design/Materials and Methods We examined the effect of 3mW red (630nm, 1J/cm super(2)), 2mW green (522nm, 1J/cm super(2)), and 2mW blue light (463nm, 1J/cm super(2)) on telogen in mice for 3 weeks. The photobiologic effects of red light on cell proliferation of outer root sheath keratinocytes and dermal papilla cells were studied in vitro. Results We found that red light accelerated anagen entry faster than green and blue light in mice. Red light irradiation stimulated the proliferation of both outer root sheath keratinocytes and dermal papilla cells in a dose-dependent manner by promoting cell cycle progression. This stimulative effect was mediated via extracellular signal-regulated kinase phosphorylation in both cells. In a co-culture condition, dermal papilla cells irradiated by red light further enhanced keratinocyte proliferation, suggesting enhanced epithelial-mesenchymal interaction. In search for factors that mediated this paracrine effect, we found fibroblast growth factor 7 was upregulated in both mRNA and protein levels. The stimulative paracrine effect on keratinocytes was significantly inhibited by neutralizing antibody against fibroblast growth factor 7. Conclusions These results suggest that hair follicles respond to visible light in vivo. Red light may promote physiological telogen to anagen transition by directly stimulating outer root sheath keratinocytes and indirectly by enhancing epithelial-mesenchymal interaction in vitro. Lasers Surg. Med. 47:50-59, 2015. copyright 2014 Wiley Periodicals, Inc.
Background and Objectives Hair follicles are located at the interface of the external and internal environments and their cycling has been shown to be regulated by intra‐ and extra‐follicular factors. The aim of this study is to examine whether or how hair follicles respond to visible light. Study Design/Materials and Methods We examined the effect of 3 mW red (630 nm, 1 J/cm 2 ), 2 mW green (522 nm, 1 J/cm 2 ), and 2 mW blue light (463 nm, 1 J/cm 2 ) on telogen in mice for 3 weeks. The photobiologic effects of red light on cell proliferation of outer root sheath keratinocytes and dermal papilla cells were studied in vitro . Results We found that red light accelerated anagen entry faster than green and blue light in mice. Red light irradiation stimulated the proliferation of both outer root sheath keratinocytes and dermal papilla cells in a dose‐dependent manner by promoting cell cycle progression. This stimulative effect was mediated via extracellular signal‐regulated kinase phosphorylation in both cells. In a co‐culture condition, dermal papilla cells irradiated by red light further enhanced keratinocyte proliferation, suggesting enhanced epithelial‐mesenchymal interaction. In search for factors that mediated this paracrine effect, we found fibroblast growth factor 7 was upregulated in both mRNA and protein levels. The stimulative paracrine effect on keratinocytes was significantly inhibited by neutralizing antibody against fibroblast growth factor 7. Conclusions These results suggest that hair follicles respond to visible light in vivo . Red light may promote physiological telogen to anagen transition by directly stimulating outer root sheath keratinocytes and indirectly by enhancing epithelial‐mesenchymal interaction in vitro . Lasers Surg. Med. 47:50–59, 2015. © 2014 Wiley Periodicals, Inc.
Background and Objectives Hair follicles are located at the interface of the external and internal environments and their cycling has been shown to be regulated by intra‐ and extra‐follicular factors. The aim of this study is to examine whether or how hair follicles respond to visible light. Study Design/Materials and Methods We examined the effect of 3 mW red (630 nm, 1 J/cm2), 2 mW green (522 nm, 1 J/cm2), and 2 mW blue light (463 nm, 1 J/cm2) on telogen in mice for 3 weeks. The photobiologic effects of red light on cell proliferation of outer root sheath keratinocytes and dermal papilla cells were studied in vitro. Results We found that red light accelerated anagen entry faster than green and blue light in mice. Red light irradiation stimulated the proliferation of both outer root sheath keratinocytes and dermal papilla cells in a dose‐dependent manner by promoting cell cycle progression. This stimulative effect was mediated via extracellular signal‐regulated kinase phosphorylation in both cells. In a co‐culture condition, dermal papilla cells irradiated by red light further enhanced keratinocyte proliferation, suggesting enhanced epithelial‐mesenchymal interaction. In search for factors that mediated this paracrine effect, we found fibroblast growth factor 7 was upregulated in both mRNA and protein levels. The stimulative paracrine effect on keratinocytes was significantly inhibited by neutralizing antibody against fibroblast growth factor 7. Conclusions These results suggest that hair follicles respond to visible light in vivo. Red light may promote physiological telogen to anagen transition by directly stimulating outer root sheath keratinocytes and indirectly by enhancing epithelial‐mesenchymal interaction in vitro. Lasers Surg. Med. 47:50–59, 2015. © 2014 Wiley Periodicals, Inc.
Author Jee, Shiou-Hwa
Fan, Sabrina Mai-Yi
Wu, Yueh-Feng
Chan, Chih-Chieh
Sheen, Yi-Shuan
Lin, Sung-Jan
Author_xml – sequence: 1
  givenname: Yi-Shuan
  surname: Sheen
  fullname: Sheen, Yi-Shuan
  organization: Department of Dermatology, National Taiwan University Hospital and National Taiwan University College of Medicine, 7 Chung-Shan South Road, 100, Taipei, Taiwan
– sequence: 2
  givenname: Sabrina Mai-Yi
  surname: Fan
  fullname: Fan, Sabrina Mai-Yi
  organization: Institute of Biomedical Engineering, College of Medicine and College of Engineering, National Taiwan University, No. 1, Sec. 1, Jen-Ai Road, 100, Taipei, Taiwan
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  givenname: Chih-Chieh
  surname: Chan
  fullname: Chan, Chih-Chieh
  organization: Department of Dermatology, National Taiwan University Hospital and National Taiwan University College of Medicine, 7 Chung-Shan South Road, 100, Taipei, Taiwan
– sequence: 4
  givenname: Yueh-Feng
  surname: Wu
  fullname: Wu, Yueh-Feng
  organization: Institute of Biomedical Engineering, College of Medicine and College of Engineering, National Taiwan University, No. 1, Sec. 1, Jen-Ai Road, 100, Taipei, Taiwan
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  givenname: Shiou-Hwa
  surname: Jee
  fullname: Jee, Shiou-Hwa
  organization: Department of Dermatology, National Taiwan University Hospital and National Taiwan University College of Medicine, 7 Chung-Shan South Road, 100, Taipei, Taiwan
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  givenname: Sung-Jan
  surname: Lin
  fullname: Lin, Sung-Jan
  email: Correspondence to: Sung-Jan Lin, MD, PhD, Department of Dermatology, National Taiwan University Hospital, 7 Chung-Shan South Road, Taipei 100, Taiwan., drsjlin@ntu.edu.tw
  organization: Department of Dermatology, National Taiwan University Hospital and National Taiwan University College of Medicine, 7 Chung-Shan South Road, 100, Taipei, Taiwan
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Keywords outer root sheath keratinocytes
FGF7
hair cycle
dermal papilla cells
Language English
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PublicationTitle Lasers in surgery and medicine
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2001; 187
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2008; 29
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2001; 19
2014; 15
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2014; 12
2012; 20
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2013; 45
2014; 46
1993; 90
2000; 156
1996; 59
2011; 8
2011; 332
1996; 10
1996; 54
1987; 18
2009; 29
1996; 205
2001; 81
2011; 146
2013; 39
2003; 24
2010; 130
2014
2009; 4
2008; 451
2011; 145
2001; 117
2012; 8
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Snippet Background and Objectives Hair follicles are located at the interface of the external and internal environments and their cycling has been shown to be...
Hair follicles are located at the interface of the external and internal environments and their cycling has been shown to be regulated by intra- and...
Background and Objectives Hair follicles are located at the interface of the external and internal environments and their cycling has been shown to be...
BACKGROUND AND OBJECTIVESHair follicles are located at the interface of the external and internal environments and their cycling has been shown to be regulated...
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SubjectTerms Animals
Biomarkers - metabolism
Cell Proliferation - radiation effects
dermal papilla cells
Dermis - metabolism
Dermis - radiation effects
Female
FGF7
Fibroblast Growth Factor 7 - metabolism
Hair - growth & development
Hair - radiation effects
hair cycle
Hair Follicle - physiology
Hair Follicle - radiation effects
In Vitro Techniques
Keratinocytes - metabolism
Keratinocytes - radiation effects
Light
Mice
Mice, Inbred C57BL
outer root sheath keratinocytes
Random Allocation
Title Visible red light enhances physiological anagen entry in vivo and has direct and indirect stimulative effects in vitro
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https://onlinelibrary.wiley.com/doi/abs/10.1002%2Flsm.22316
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https://www.proquest.com/docview/1647027802/abstract/
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https://search.proquest.com/docview/1654696389
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