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...

Full description

Bibliographic Details
Main Authors: Jihye Seong, Min Huang, Kyoung Mi Sim, Hyunbin Kim, Yingxiao Wang
Format: Article
Language:English
Published: Nature Publishing Group 2017-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-01789-y
id doaj-e7b1f343f0644c62b19da8aeeb3d4935
record_format Article
spelling 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 AT jihyeseong fretbasedvisualizationofpdgfreceptoractivationatmembranemicrodomains
AT minhuang fretbasedvisualizationofpdgfreceptoractivationatmembranemicrodomains
AT kyoungmisim fretbasedvisualizationofpdgfreceptoractivationatmembranemicrodomains
AT hyunbinkim fretbasedvisualizationofpdgfreceptoractivationatmembranemicrodomains
AT yingxiaowang fretbasedvisualizationofpdgfreceptoractivationatmembranemicrodomains
_version_ 1724394843018362880