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Identification of PLXDC1 and PLXDC2 as the transmembrane receptors for the multifunctional factor PEDF
Pigment Epithelium Derived Factor (PEDF) is a secreted factor that has broad biological activities. It was first identified as a neurotrophic factor and later as the most potent natural antiangiogenic factor, a stem cell niche factor, and an inhibitor of cancer cell growth. Numerous animal models de...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303762/ https://www.ncbi.nlm.nih.gov/pubmed/25535841 http://dx.doi.org/10.7554/eLife.05401 |
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author | Cheng, Guo Zhong, Ming Kawaguchi, Riki Kassai, Miki Al-Ubaidi, Muayyad Deng, Jun Ter-Stepanian, Mariam Sun, Hui |
author_facet | Cheng, Guo Zhong, Ming Kawaguchi, Riki Kassai, Miki Al-Ubaidi, Muayyad Deng, Jun Ter-Stepanian, Mariam Sun, Hui |
author_sort | Cheng, Guo |
collection | PubMed |
description | Pigment Epithelium Derived Factor (PEDF) is a secreted factor that has broad biological activities. It was first identified as a neurotrophic factor and later as the most potent natural antiangiogenic factor, a stem cell niche factor, and an inhibitor of cancer cell growth. Numerous animal models demonstrated its therapeutic value in treating blinding diseases and diverse cancer types. A long-standing challenge is to reveal how PEDF acts on its target cells and the identities of the cell-surface receptors responsible for its activities. Here we report the identification of transmembrane proteins PLXDC1 and PLXDC2 as cell-surface receptors for PEDF. Using distinct cellular models, we demonstrate their cell type-specific receptor activities through loss of function and gain of function studies. Our experiments suggest that PEDF receptors form homooligomers under basal conditions, and PEDF dissociates the homooligomer to activate the receptors. Mutations in the intracellular domain can have profound effects on receptor activities. DOI: http://dx.doi.org/10.7554/eLife.05401.001 |
format | Online Article Text |
id | pubmed-4303762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-43037622015-01-29 Identification of PLXDC1 and PLXDC2 as the transmembrane receptors for the multifunctional factor PEDF Cheng, Guo Zhong, Ming Kawaguchi, Riki Kassai, Miki Al-Ubaidi, Muayyad Deng, Jun Ter-Stepanian, Mariam Sun, Hui eLife Biochemistry Pigment Epithelium Derived Factor (PEDF) is a secreted factor that has broad biological activities. It was first identified as a neurotrophic factor and later as the most potent natural antiangiogenic factor, a stem cell niche factor, and an inhibitor of cancer cell growth. Numerous animal models demonstrated its therapeutic value in treating blinding diseases and diverse cancer types. A long-standing challenge is to reveal how PEDF acts on its target cells and the identities of the cell-surface receptors responsible for its activities. Here we report the identification of transmembrane proteins PLXDC1 and PLXDC2 as cell-surface receptors for PEDF. Using distinct cellular models, we demonstrate their cell type-specific receptor activities through loss of function and gain of function studies. Our experiments suggest that PEDF receptors form homooligomers under basal conditions, and PEDF dissociates the homooligomer to activate the receptors. Mutations in the intracellular domain can have profound effects on receptor activities. DOI: http://dx.doi.org/10.7554/eLife.05401.001 eLife Sciences Publications, Ltd 2014-12-23 /pmc/articles/PMC4303762/ /pubmed/25535841 http://dx.doi.org/10.7554/eLife.05401 Text en © 2014, Cheng et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry Cheng, Guo Zhong, Ming Kawaguchi, Riki Kassai, Miki Al-Ubaidi, Muayyad Deng, Jun Ter-Stepanian, Mariam Sun, Hui Identification of PLXDC1 and PLXDC2 as the transmembrane receptors for the multifunctional factor PEDF |
title | Identification of PLXDC1 and PLXDC2 as the transmembrane receptors for the multifunctional factor PEDF |
title_full | Identification of PLXDC1 and PLXDC2 as the transmembrane receptors for the multifunctional factor PEDF |
title_fullStr | Identification of PLXDC1 and PLXDC2 as the transmembrane receptors for the multifunctional factor PEDF |
title_full_unstemmed | Identification of PLXDC1 and PLXDC2 as the transmembrane receptors for the multifunctional factor PEDF |
title_short | Identification of PLXDC1 and PLXDC2 as the transmembrane receptors for the multifunctional factor PEDF |
title_sort | identification of plxdc1 and plxdc2 as the transmembrane receptors for the multifunctional factor pedf |
topic | Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4303762/ https://www.ncbi.nlm.nih.gov/pubmed/25535841 http://dx.doi.org/10.7554/eLife.05401 |
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