FRET-based Visualization of PDGF Receptor Activation at Membrane Microdomains
Abstract Platelet-derived growth factor receptor (PDGFR) senses extracellular growth factors and transfer the signals inside the cells regulating cell proliferation, migration and survival. It has been controversial at which membrane microdomains PDGFRs reside and how they control such diverse intra...
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Online Access: | https://doi.org/10.1038/s41598-017-01789-y |
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doaj-e7b1f343f0644c62b19da8aeeb3d49352020-12-08T01:29:29ZengNature Publishing GroupScientific Reports2045-23222017-05-017111110.1038/s41598-017-01789-yFRET-based Visualization of PDGF Receptor Activation at Membrane MicrodomainsJihye Seong0Min Huang1Kyoung Mi Sim2Hyunbin Kim3Yingxiao Wang4Neuroscience Program, University of Illinois, Urbana-ChampaignDepartment of Bioengineering, University of Illinois, Urbana-ChampaignConvergence Research Center for Diagnosis Treatment Care of Dementia, Korea Institute of Science and Technology (KIST)Convergence Research Center for Diagnosis Treatment Care of Dementia, Korea Institute of Science and Technology (KIST)Neuroscience Program, University of Illinois, Urbana-ChampaignAbstract Platelet-derived growth factor receptor (PDGFR) senses extracellular growth factors and transfer the signals inside the cells regulating cell proliferation, migration and survival. It has been controversial at which membrane microdomains PDGFRs reside and how they control such diverse intracellular signaling pathways. Here, we developed a novel PDGFR biosensor based on fluorescence resonance energy transfer (FRET), which can detect the real-time PDGFR activity in live cells with high spatiotemporal resolutions. To study subcellular PDGFR activity at membrane microdomains, this PDGFR biosensor was further targeted in or outside lipid rafts via different lipid modification signals. The results suggest that, in response to PDGF stimulation, PDGFR activity is evenly distributed at different membrane microdomains, while integrin-mediated signaling events have inhibitory effects on the activation of PDGFR specifically located in lipid rafts but not outside rafts, implying the role of lipid microdomains as segregated signaling platforms.https://doi.org/10.1038/s41598-017-01789-y |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jihye Seong Min Huang Kyoung Mi Sim Hyunbin Kim Yingxiao Wang |
spellingShingle |
Jihye Seong Min Huang Kyoung Mi Sim Hyunbin Kim Yingxiao Wang FRET-based Visualization of PDGF Receptor Activation at Membrane Microdomains Scientific Reports |
author_facet |
Jihye Seong Min Huang Kyoung Mi Sim Hyunbin Kim Yingxiao Wang |
author_sort |
Jihye Seong |
title |
FRET-based Visualization of PDGF Receptor Activation at Membrane Microdomains |
title_short |
FRET-based Visualization of PDGF Receptor Activation at Membrane Microdomains |
title_full |
FRET-based Visualization of PDGF Receptor Activation at Membrane Microdomains |
title_fullStr |
FRET-based Visualization of PDGF Receptor Activation at Membrane Microdomains |
title_full_unstemmed |
FRET-based Visualization of PDGF Receptor Activation at Membrane Microdomains |
title_sort |
fret-based visualization of pdgf receptor activation at membrane microdomains |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2017-05-01 |
description |
Abstract Platelet-derived growth factor receptor (PDGFR) senses extracellular growth factors and transfer the signals inside the cells regulating cell proliferation, migration and survival. It has been controversial at which membrane microdomains PDGFRs reside and how they control such diverse intracellular signaling pathways. Here, we developed a novel PDGFR biosensor based on fluorescence resonance energy transfer (FRET), which can detect the real-time PDGFR activity in live cells with high spatiotemporal resolutions. To study subcellular PDGFR activity at membrane microdomains, this PDGFR biosensor was further targeted in or outside lipid rafts via different lipid modification signals. The results suggest that, in response to PDGF stimulation, PDGFR activity is evenly distributed at different membrane microdomains, while integrin-mediated signaling events have inhibitory effects on the activation of PDGFR specifically located in lipid rafts but not outside rafts, implying the role of lipid microdomains as segregated signaling platforms. |
url |
https://doi.org/10.1038/s41598-017-01789-y |
work_keys_str_mv |
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