Epidermal expression of neuropilin 1 protects murine keratinocytes from UVB-induced apoptosis.

BACKGROUND: Neuropilin 1 (NRP1) is expressed on several cell types including neurons and endothelial cells, where it functions as an important regulator in development and during angiogenesis. As a cell surface receptor, NRP1 is able to bind to members of the VEGF family of growth factors and to sec...

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Main Authors: Anna Riese, Yvonne Eilert, Yvonne Meyer, Meral Arin, Jens M Baron, Sabine Eming, Thomas Krieg, Peter Kurschat
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3518474?pdf=render
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author Anna Riese
Yvonne Eilert
Yvonne Meyer
Meral Arin
Jens M Baron
Sabine Eming
Thomas Krieg
Peter Kurschat
author_facet Anna Riese
Yvonne Eilert
Yvonne Meyer
Meral Arin
Jens M Baron
Sabine Eming
Thomas Krieg
Peter Kurschat
author_sort Anna Riese
collection DOAJ
description BACKGROUND: Neuropilin 1 (NRP1) is expressed on several cell types including neurons and endothelial cells, where it functions as an important regulator in development and during angiogenesis. As a cell surface receptor, NRP1 is able to bind to members of the VEGF family of growth factors and to secreted class 3 semaphorins. Neuropilin 1 is also highly expressed in keratinocytes, but the function of NRP1 in epidermal physiology and pathology is still unclear. METHODS AND RESULTS: To elucidate the role of NRP1 in skin in vivo we generated an epidermis-specific neuropilin 1 knock out mouse model by using the Cre-LoxP-System. Mice were viable and fertile and did not display any obvious skin or hair defects. After challenge with UVB irradiation, we found that deletion of epidermal NRP1 leads to increased rates of apoptosis both in vitro and in vivo. NRP1-deficient primary keratinocytes cultured in vitro showed significantly higher rates of apoptosis 24 hours after UVB. Likewise, there is a significant increase of active caspase 3 positive cells in the epidermis of Keratin 14-Cre-NRP1 (-/-) mice 24 hours after UVB irradiation. By Western Blot analysis we could show that NRP1 influences the cytosolic levels of Bcl-2, a pro-survival member of the Bcl-2 family. After UVB irradiation the amounts of Bcl-2 decrease in both protein extracts from murine epidermis and in NRP1-deficient keratinocytes in vitro, whereas wild type cells retain their Bcl-2 levels. Likewise, levels of phospho-Erk and Rac1 were lower in NRP1-knock out keratinocytes, whereas levels of pro-apoptotic p53 were higher. CONCLUSION: NRP1 expression in keratinocytes is dispensable for normal skin development. Upon UVB challenge, NRP1 contributes to the prevention of keratinocyte apoptosis. This pro-survival function of NRP1 is accompanied by the maintenance of high levels of the antiapoptotic regulator Bcl-2 and by lower levels of pro-apoptotic p53.
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spelling doaj.art-5d794bec084a4480aa070ea6dbcadc552022-12-21T23:56:42ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01712e5094410.1371/journal.pone.0050944Epidermal expression of neuropilin 1 protects murine keratinocytes from UVB-induced apoptosis.Anna RieseYvonne EilertYvonne MeyerMeral ArinJens M BaronSabine EmingThomas KriegPeter KurschatBACKGROUND: Neuropilin 1 (NRP1) is expressed on several cell types including neurons and endothelial cells, where it functions as an important regulator in development and during angiogenesis. As a cell surface receptor, NRP1 is able to bind to members of the VEGF family of growth factors and to secreted class 3 semaphorins. Neuropilin 1 is also highly expressed in keratinocytes, but the function of NRP1 in epidermal physiology and pathology is still unclear. METHODS AND RESULTS: To elucidate the role of NRP1 in skin in vivo we generated an epidermis-specific neuropilin 1 knock out mouse model by using the Cre-LoxP-System. Mice were viable and fertile and did not display any obvious skin or hair defects. After challenge with UVB irradiation, we found that deletion of epidermal NRP1 leads to increased rates of apoptosis both in vitro and in vivo. NRP1-deficient primary keratinocytes cultured in vitro showed significantly higher rates of apoptosis 24 hours after UVB. Likewise, there is a significant increase of active caspase 3 positive cells in the epidermis of Keratin 14-Cre-NRP1 (-/-) mice 24 hours after UVB irradiation. By Western Blot analysis we could show that NRP1 influences the cytosolic levels of Bcl-2, a pro-survival member of the Bcl-2 family. After UVB irradiation the amounts of Bcl-2 decrease in both protein extracts from murine epidermis and in NRP1-deficient keratinocytes in vitro, whereas wild type cells retain their Bcl-2 levels. Likewise, levels of phospho-Erk and Rac1 were lower in NRP1-knock out keratinocytes, whereas levels of pro-apoptotic p53 were higher. CONCLUSION: NRP1 expression in keratinocytes is dispensable for normal skin development. Upon UVB challenge, NRP1 contributes to the prevention of keratinocyte apoptosis. This pro-survival function of NRP1 is accompanied by the maintenance of high levels of the antiapoptotic regulator Bcl-2 and by lower levels of pro-apoptotic p53.http://europepmc.org/articles/PMC3518474?pdf=render
spellingShingle Anna Riese
Yvonne Eilert
Yvonne Meyer
Meral Arin
Jens M Baron
Sabine Eming
Thomas Krieg
Peter Kurschat
Epidermal expression of neuropilin 1 protects murine keratinocytes from UVB-induced apoptosis.
PLoS ONE
title Epidermal expression of neuropilin 1 protects murine keratinocytes from UVB-induced apoptosis.
title_full Epidermal expression of neuropilin 1 protects murine keratinocytes from UVB-induced apoptosis.
title_fullStr Epidermal expression of neuropilin 1 protects murine keratinocytes from UVB-induced apoptosis.
title_full_unstemmed Epidermal expression of neuropilin 1 protects murine keratinocytes from UVB-induced apoptosis.
title_short Epidermal expression of neuropilin 1 protects murine keratinocytes from UVB-induced apoptosis.
title_sort epidermal expression of neuropilin 1 protects murine keratinocytes from uvb induced apoptosis
url http://europepmc.org/articles/PMC3518474?pdf=render
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