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Main Authors: Fei Yang, Lingli Yang, Yasutaka Kuroda, Sylvia Lai, Yoshito Takahashi, Tetsuya Sayo, Takeshi Namiki, Kimiko Nakajima, Shigetoshi Sano, Shintaro Inoue, Daisuke Tsuruta, Ichiro Katayama
Format: Artículo Open Access
Published: Wiley 2024
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Online Access:https://pathsocjournals.onlinelibrary.wiley.com/doi/10.1002/path.6321
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author Fei Yang
Lingli Yang
Yasutaka Kuroda
Sylvia Lai
Yoshito Takahashi
Tetsuya Sayo
Takeshi Namiki
Kimiko Nakajima
Shigetoshi Sano
Shintaro Inoue
Daisuke Tsuruta
Ichiro Katayama
author_facet Fei Yang
Lingli Yang
Yasutaka Kuroda
Sylvia Lai
Yoshito Takahashi
Tetsuya Sayo
Takeshi Namiki
Kimiko Nakajima
Shigetoshi Sano
Shintaro Inoue
Daisuke Tsuruta
Ichiro Katayama
Fei Yang
Lingli Yang
Yasutaka Kuroda
Sylvia Lai
Yoshito Takahashi
Tetsuya Sayo
Takeshi Namiki
Kimiko Nakajima
Shigetoshi Sano
Shintaro Inoue
Daisuke Tsuruta
Ichiro Katayama
collection Wiley Open Access
contents Disorganisation of basement membrane zone architecture impairs melanocyte residence in vitiligo Fei Yang Lingli Yang Yasutaka Kuroda Sylvia Lai Yoshito Takahashi Tetsuya Sayo Takeshi Namiki Kimiko Nakajima Shigetoshi Sano Shintaro Inoue Daisuke Tsuruta Ichiro Katayama The Journal of Pathology AbstractThe basement membrane zone is the interface between the epidermis and dermis, and it is disrupted in several skin conditions. Here, we report the results of a comprehensive investigation into the structural and molecular factors of the basement membrane zone in vitiligo, a dermatological disorder characterised by depigmented patches on the skin. Using electron microscopy and immunofluorescence staining, we confirmed abnormal basement membrane zone morphology and disrupted basement membrane zone architecture in human vitiliginous skin. Furthermore, we identified elevated expression of matrix metalloproteinase 2 (MMP2) in human dermal fibroblasts as a key factor responsible for basement membrane zone matrix degradation. In our in vitro and ex vivo models, overexpression of MMP2 in fibroblasts led to basement membrane zone disruption and melanocyte disappearance. Importantly, we reveal that the loss of melanocytes in vitiligo is primarily linked to their weakened adhesion to the basement membrane, mediated by binding between integrin β1 and laminin and discoidin domain receptor 1 and collagen IV. Finally, inhibition of matrix metalloproteinase 2 expression reversed depigmentation in a mouse model of vitiligo. In conclusion, our research shows the importance of basement membrane zone integrity in melanocyte residence and offers new avenues for therapeutic interventions to address this challenging skin condition. © 2024 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland. 10.1002/path.6321 http://creativecommons.org/licenses/by-nc-nd/4.0/
doi_str_mv 10.1002/path.6321
format Artículo Open Access
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institution Wiley Open Access
license_str_mv http://creativecommons.org/licenses/by-nc-nd/4.0/
publishDate 2024
publisher Wiley
record_format wiley_oa
spellingShingle Disorganisation of basement membrane zone architecture impairs melanocyte residence in vitiligo
Fei Yang
Lingli Yang
Yasutaka Kuroda
Sylvia Lai
Yoshito Takahashi
Tetsuya Sayo
Takeshi Namiki
Kimiko Nakajima
Shigetoshi Sano
Shintaro Inoue
Daisuke Tsuruta
Ichiro Katayama
The Journal of Pathology
Disorganisation of basement membrane zone architecture impairs melanocyte residence in vitiligo Fei Yang Lingli Yang Yasutaka Kuroda Sylvia Lai Yoshito Takahashi Tetsuya Sayo Takeshi Namiki Kimiko Nakajima Shigetoshi Sano Shintaro Inoue Daisuke Tsuruta Ichiro Katayama The Journal of Pathology AbstractThe basement membrane zone is the interface between the epidermis and dermis, and it is disrupted in several skin conditions. Here, we report the results of a comprehensive investigation into the structural and molecular factors of the basement membrane zone in vitiligo, a dermatological disorder characterised by depigmented patches on the skin. Using electron microscopy and immunofluorescence staining, we confirmed abnormal basement membrane zone morphology and disrupted basement membrane zone architecture in human vitiliginous skin. Furthermore, we identified elevated expression of matrix metalloproteinase 2 (MMP2) in human dermal fibroblasts as a key factor responsible for basement membrane zone matrix degradation. In our in vitro and ex vivo models, overexpression of MMP2 in fibroblasts led to basement membrane zone disruption and melanocyte disappearance. Importantly, we reveal that the loss of melanocytes in vitiligo is primarily linked to their weakened adhesion to the basement membrane, mediated by binding between integrin β1 and laminin and discoidin domain receptor 1 and collagen IV. Finally, inhibition of matrix metalloproteinase 2 expression reversed depigmentation in a mouse model of vitiligo. In conclusion, our research shows the importance of basement membrane zone integrity in melanocyte residence and offers new avenues for therapeutic interventions to address this challenging skin condition. © 2024 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland. 10.1002/path.6321 http://creativecommons.org/licenses/by-nc-nd/4.0/
title Disorganisation of basement membrane zone architecture impairs melanocyte residence in vitiligo
topic The Journal of Pathology
url https://pathsocjournals.onlinelibrary.wiley.com/doi/10.1002/path.6321