Home LiteratureArticle Details
PMID: 15944146 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, P.H.S.

Platelet-derived growth factor receptor-beta (PDGFR-beta) activation promotes its association with the low density lipoprotein receptor-related protein (LRP). Evidence for co-receptor function.

The Journal of biological chemistry ·Vol. 280 ·No. 30 ·2005-07-29 ·Pages 27872-8

Newton CS, Loukinova E, Mikhailenko I, Ranganathan S, Gao Y, Haudenschild C, Strickland DK

Abstract

Activation of the platelet-derived growth factor receptor-beta (PDGFR-beta) leads to tyrosine phosphorylation of the cytoplasmic domain of LRP and alters its association with adaptor and signaling proteins, such as Shc. The mechanism of the PDGF-induced LRP tyrosine phosphorylation is not well understood, especially since PDGF not only activates PDGF receptor but also binds directly to LRP. To gain insight into this mechanism, we used a chimeric receptor in which the ligand binding domain of the PDGFR-beta was replaced with that from the macrophage colony-stimulating factor (M-CSF) receptor, a highly related receptor tyrosine kinase of the same subfamily, but with different ligand specificity. Activation of the chimeric receptor upon the addition of M-CSF readily mediated the tyrosine phosphorylation of LRP. Since M-CSF is not recognized by LRP, these results indicated that growth factor binding to LRP is not necessary for this phosphorylation event. Using a panel of cytoplasmic domain mutants of the chimeric M-CSF/PDGFR-beta, we confirmed that the kinase domain of PDGFR-beta is absolutely required for LRP tyrosine phosphorylation but that PDGFR-beta-mediated activation of phosphatidylinositol 3-kinase, RasGAP, SHP-2, phospholipase C-gamma, and Src are not necessary for LRP tyrosine phosphorylation. To identify the cellular compartment where LRP and the PDGFR-beta may interact, we employed immunofluorescence and immunogold electron microscopy. In WI-38 fibroblasts, these two receptors co-localized in coated pits and endosomal compartments following PDGF stimulation. Further, phosphorylated forms of the PDGFR-beta co-immunoprecipitated with LRP following PDGF treatment. Together, these studies revealed close association between activated PDGFR-beta and LRP, suggesting that LRP functions as a co-receptor capable of modulating the signal transduction pathways initiated by the PDGF receptor from endosomes.

MeSH Terms
Animals Cytoplasm/metabolism Endosomes/metabolism Fibroblasts/metabolism Humans Immunohistochemistry Immunoprecipitation Intracellular Signaling Peptides and Proteins/metabolism Ligands Low Density Lipoprotein Receptor-Related Protein-1/metabolism Mice Microscopy, Fluorescence Mutation NIH 3T3 Cells Phosphatidylinositol 3-Kinases/metabolism Phospholipase C gamma Phosphorylation Protein Binding Protein Structure, Tertiary Protein Tyrosine Phosphatase, Non-Receptor Type 11 Protein Tyrosine Phosphatases/metabolism Receptor, Macrophage Colony-Stimulating Factor/metabolism Receptor, Platelet-Derived Growth Factor beta/metabolism Recombinant Fusion Proteins/metabolism Signal Transduction Time Factors Type C Phospholipases/metabolism Tyrosine/chemistry,metabolism ras GTPase-Activating Proteins/metabolism
Chemicals
Intracellular Signaling Peptides and Proteins Ligands Low Density Lipoprotein Receptor-Related Protein-1 Recombinant Fusion Proteins ras GTPase-Activating Proteins Tyrosine Phosphatidylinositol 3-Kinases Receptor, Macrophage Colony-Stimulating Factor Receptor, Platelet-Derived Growth Factor beta PTPN11 protein, human Protein Tyrosine Phosphatase, Non-Receptor Type 11 Protein Tyrosine Phosphatases Ptpn11 protein, mouse Type C Phospholipases Phospholipase C gamma
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Newton Christopher S
Department of Surgery and Physiology, University of Maryland School of Medicine, 15601 Crabbs Branch Way, Rockville, Maryland 20855, USA.
Loukinova Elena
Mikhailenko Irina
Ranganathan Sripriya
Gao Yamei
Haudenschild Christian
Strickland Dudley K
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2005-07-29
Epub
2005-00-08
Pages
27872-8
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NHLBI NIH HHS · HL50784 · United States
NHLBI NIH HHS · HL54710 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]