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CD9 negatively regulates collective electrotaxis of the epidermal monolayer by controlling and coordinating the polarization of leader cells

BACKGROUND: Endogenous electric fields (EFs) play an essential role in guiding the coordinated collective migration of epidermal cells to the wound centre during wound healing. Although polarization of leadercells is essential for collective migration, the signal mechanisms responsible for the EF-in...

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Autores principales: Liu, Xiaoqiang, Yang, Jinrui, Kong, Meng, Jiang, Min, Liu, Luojia, Zhang, Jinghong, Chen, Ying, Chen, Xu, Zhang, Ze, Wu, Chao, Jiang, Xupin, Liu, Jie, Zhang, Jiaping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10365154/
https://www.ncbi.nlm.nih.gov/pubmed/37492637
http://dx.doi.org/10.1093/burnst/tkad012
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author Liu, Xiaoqiang
Yang, Jinrui
Kong, Meng
Jiang, Min
Liu, Luojia
Zhang, Jinghong
Chen, Ying
Chen, Xu
Zhang, Ze
Wu, Chao
Jiang, Xupin
Liu, Jie
Zhang, Jiaping
author_facet Liu, Xiaoqiang
Yang, Jinrui
Kong, Meng
Jiang, Min
Liu, Luojia
Zhang, Jinghong
Chen, Ying
Chen, Xu
Zhang, Ze
Wu, Chao
Jiang, Xupin
Liu, Jie
Zhang, Jiaping
author_sort Liu, Xiaoqiang
collection PubMed
description BACKGROUND: Endogenous electric fields (EFs) play an essential role in guiding the coordinated collective migration of epidermal cells to the wound centre during wound healing. Although polarization of leadercells is essential for collective migration, the signal mechanisms responsible for the EF-induced polarization of leader cells under electrotactic collective migration remain unclear. This study aims to determine how the leader cells are polarized and coordinated during EF-guided collective migration of epidermal cell sheets. METHODS: Collective migration of the human epidermal monolayer (human immortalized keratinocytes HaCaT) under EFs was observed via time-lapse microscopy. The involvement of tetraspanin-29 (CD9) in EF-induced fibrous actin (F-actin) polarization of leader cells as well as electrotactic migration of the epidermal monolayer was evaluated by genetic manipulation. Blocking, rescue and co-culture experiments were conducted to explore the downstream signalling of CD9. RESULTS: EFs guided the coordinated collective migration of the epithelial monolayer to the anode, with dynamic formation of pseudopodia in leader cells at the front edge of the monolayer along the direction of migration. F-actin polarization, as expected, played an essential role in pseudopod formation in leader cells under EFs. By confocal microscopy, we found that CD9 was colocalized with F-actin on the cell surface and was particularly downregulated in leader cells by EFs. Interestingly, genetic overexpression of CD9 abolished EF-induced F-actin polarization in leader cells as well as collective migration in the epidermal monolayer. Mechanistically, CD9 determined the polarization of F-actin in leader cells by downregulating a disintegrin and metalloprotease 17/heparin-binding epidermal growth factor-like growth factor/epidermal growth factor receptor (ADAM17/HB-EGF/EGFR) signalling. The abolished polarization of leader cells due to CD9 overexpression could be restored in a co-culture monolayer where normal cells and CD9-overexpressing cells were mixed; however, this restoration was eliminated again by the addition of the HB-EGF-neutralizing antibody. CONCLUSION: CD9 functions as a key regulator in the EF-guided collective migration of the epidermal monolayer by controlling and coordinating the polarization of leader cells through ADAM17/HB-EGF/EGFR signalling.
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spelling pubmed-103651542023-07-25 CD9 negatively regulates collective electrotaxis of the epidermal monolayer by controlling and coordinating the polarization of leader cells Liu, Xiaoqiang Yang, Jinrui Kong, Meng Jiang, Min Liu, Luojia Zhang, Jinghong Chen, Ying Chen, Xu Zhang, Ze Wu, Chao Jiang, Xupin Liu, Jie Zhang, Jiaping Burns Trauma Research Article BACKGROUND: Endogenous electric fields (EFs) play an essential role in guiding the coordinated collective migration of epidermal cells to the wound centre during wound healing. Although polarization of leadercells is essential for collective migration, the signal mechanisms responsible for the EF-induced polarization of leader cells under electrotactic collective migration remain unclear. This study aims to determine how the leader cells are polarized and coordinated during EF-guided collective migration of epidermal cell sheets. METHODS: Collective migration of the human epidermal monolayer (human immortalized keratinocytes HaCaT) under EFs was observed via time-lapse microscopy. The involvement of tetraspanin-29 (CD9) in EF-induced fibrous actin (F-actin) polarization of leader cells as well as electrotactic migration of the epidermal monolayer was evaluated by genetic manipulation. Blocking, rescue and co-culture experiments were conducted to explore the downstream signalling of CD9. RESULTS: EFs guided the coordinated collective migration of the epithelial monolayer to the anode, with dynamic formation of pseudopodia in leader cells at the front edge of the monolayer along the direction of migration. F-actin polarization, as expected, played an essential role in pseudopod formation in leader cells under EFs. By confocal microscopy, we found that CD9 was colocalized with F-actin on the cell surface and was particularly downregulated in leader cells by EFs. Interestingly, genetic overexpression of CD9 abolished EF-induced F-actin polarization in leader cells as well as collective migration in the epidermal monolayer. Mechanistically, CD9 determined the polarization of F-actin in leader cells by downregulating a disintegrin and metalloprotease 17/heparin-binding epidermal growth factor-like growth factor/epidermal growth factor receptor (ADAM17/HB-EGF/EGFR) signalling. The abolished polarization of leader cells due to CD9 overexpression could be restored in a co-culture monolayer where normal cells and CD9-overexpressing cells were mixed; however, this restoration was eliminated again by the addition of the HB-EGF-neutralizing antibody. CONCLUSION: CD9 functions as a key regulator in the EF-guided collective migration of the epidermal monolayer by controlling and coordinating the polarization of leader cells through ADAM17/HB-EGF/EGFR signalling. Oxford University Press 2023-07-24 /pmc/articles/PMC10365154/ /pubmed/37492637 http://dx.doi.org/10.1093/burnst/tkad012 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Liu, Xiaoqiang
Yang, Jinrui
Kong, Meng
Jiang, Min
Liu, Luojia
Zhang, Jinghong
Chen, Ying
Chen, Xu
Zhang, Ze
Wu, Chao
Jiang, Xupin
Liu, Jie
Zhang, Jiaping
CD9 negatively regulates collective electrotaxis of the epidermal monolayer by controlling and coordinating the polarization of leader cells
title CD9 negatively regulates collective electrotaxis of the epidermal monolayer by controlling and coordinating the polarization of leader cells
title_full CD9 negatively regulates collective electrotaxis of the epidermal monolayer by controlling and coordinating the polarization of leader cells
title_fullStr CD9 negatively regulates collective electrotaxis of the epidermal monolayer by controlling and coordinating the polarization of leader cells
title_full_unstemmed CD9 negatively regulates collective electrotaxis of the epidermal monolayer by controlling and coordinating the polarization of leader cells
title_short CD9 negatively regulates collective electrotaxis of the epidermal monolayer by controlling and coordinating the polarization of leader cells
title_sort cd9 negatively regulates collective electrotaxis of the epidermal monolayer by controlling and coordinating the polarization of leader cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10365154/
https://www.ncbi.nlm.nih.gov/pubmed/37492637
http://dx.doi.org/10.1093/burnst/tkad012
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