Polyamine regulator AMD1 promotes cell migration in epidermal wound healing

Wound healing is a dynamic process involving gene-expression changes that drive re-epithelialization. Here, we describe an essential role for polyamine regulator AMD1 in driving cell migration at the wound edge. The polyamines, putrescine, spermidine, and spermine are small cationic molecules that p...

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Main Authors: Lim, Hui Kheng, Anisa Rahim, Leo, Vonny Ivon, Das, Shatarupa, Lim, Thiam Chye, Uemura, Takeshi, Igarashi, Kazuei, Common, John, Vardy, Leah Anne
Other Authors: School of Biological Sciences
Format: Article
Language:English
Published: 2020
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Online Access:https://hdl.handle.net/10356/139584
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1395842020-05-20T07:06:18Z Polyamine regulator AMD1 promotes cell migration in epidermal wound healing Lim, Hui Kheng Anisa Rahim Leo, Vonny Ivon Das, Shatarupa Lim, Thiam Chye Uemura, Takeshi Igarashi, Kazuei Common, John Vardy, Leah Anne School of Biological Sciences Science::Medicine AMD1 Cell Migration Wound healing is a dynamic process involving gene-expression changes that drive re-epithelialization. Here, we describe an essential role for polyamine regulator AMD1 in driving cell migration at the wound edge. The polyamines, putrescine, spermidine, and spermine are small cationic molecules that play essential roles in many cellular processes. We demonstrate that AMD1 is rapidly upregulated following wounding in human skin biopsies. Knockdown of AMD1 with small hairpin RNAs causes a delay in cell migration that is rescued by the addition of spermine. We further show that spermine can promote cell migration in keratinocytes and in human ex vivo wounds, where it significantly increases epithelial tongue migration. Knockdown of AMD1 prevents the upregulation of urokinase-type plasminogen activator/urokinase-type plasminogen activator receptor on wounding and results in a failure in actin cytoskeletal reorganization at the wound edge. We demonstrate that keratinocytes respond to wounding by modulating polyamine regulator AMD1 in order to regulate downstream gene expression and promote cell migration. This article highlights a previously unreported role for the regulation of polyamine levels and ratios in cellular behavior and fate. ASTAR (Agency for Sci., Tech. and Research, S’pore) 2020-05-20T07:06:18Z 2020-05-20T07:06:18Z 2018 Journal Article Lim, H. K., Anisa Rahim, Leo, V. I., Das, S., Lim, T. C., Uemura, T., . . . Vardy, L. A. (2018). Polyamine regulator AMD1 promotes cell migration in epidermal wound healing. Journal of Investigative Dermatology, 138(12), 2653-2665. doi:10.1016/j.jid.2018.05.029 0022-202X https://hdl.handle.net/10356/139584 10.1016/j.jid.2018.05.029 29906410 2-s2.0-85051485665 12 138 2653 2665 en Journal of Investigative Dermatology © 2018 The Authors (published by Elsevier, Inc. on behalf of the Society for Investigative Dermatology). All rights reserved.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic Science::Medicine
AMD1
Cell Migration
spellingShingle Science::Medicine
AMD1
Cell Migration
Lim, Hui Kheng
Anisa Rahim
Leo, Vonny Ivon
Das, Shatarupa
Lim, Thiam Chye
Uemura, Takeshi
Igarashi, Kazuei
Common, John
Vardy, Leah Anne
Polyamine regulator AMD1 promotes cell migration in epidermal wound healing
description Wound healing is a dynamic process involving gene-expression changes that drive re-epithelialization. Here, we describe an essential role for polyamine regulator AMD1 in driving cell migration at the wound edge. The polyamines, putrescine, spermidine, and spermine are small cationic molecules that play essential roles in many cellular processes. We demonstrate that AMD1 is rapidly upregulated following wounding in human skin biopsies. Knockdown of AMD1 with small hairpin RNAs causes a delay in cell migration that is rescued by the addition of spermine. We further show that spermine can promote cell migration in keratinocytes and in human ex vivo wounds, where it significantly increases epithelial tongue migration. Knockdown of AMD1 prevents the upregulation of urokinase-type plasminogen activator/urokinase-type plasminogen activator receptor on wounding and results in a failure in actin cytoskeletal reorganization at the wound edge. We demonstrate that keratinocytes respond to wounding by modulating polyamine regulator AMD1 in order to regulate downstream gene expression and promote cell migration. This article highlights a previously unreported role for the regulation of polyamine levels and ratios in cellular behavior and fate.
author2 School of Biological Sciences
author_facet School of Biological Sciences
Lim, Hui Kheng
Anisa Rahim
Leo, Vonny Ivon
Das, Shatarupa
Lim, Thiam Chye
Uemura, Takeshi
Igarashi, Kazuei
Common, John
Vardy, Leah Anne
format Article
author Lim, Hui Kheng
Anisa Rahim
Leo, Vonny Ivon
Das, Shatarupa
Lim, Thiam Chye
Uemura, Takeshi
Igarashi, Kazuei
Common, John
Vardy, Leah Anne
author_sort Lim, Hui Kheng
title Polyamine regulator AMD1 promotes cell migration in epidermal wound healing
title_short Polyamine regulator AMD1 promotes cell migration in epidermal wound healing
title_full Polyamine regulator AMD1 promotes cell migration in epidermal wound healing
title_fullStr Polyamine regulator AMD1 promotes cell migration in epidermal wound healing
title_full_unstemmed Polyamine regulator AMD1 promotes cell migration in epidermal wound healing
title_sort polyamine regulator amd1 promotes cell migration in epidermal wound healing
publishDate 2020
url https://hdl.handle.net/10356/139584
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