Abstract
Lad was previously identified as an adaptor protein binding to the SH2 domain of Lck (1). Specific detection of Lad mRNA in lung cells, as well as, in T cells led us to investigate the signaling pathways regulating Lad in lung cells. We found that (i) upon PDGF stimulation, Lad expression is induced in lung cells, especially in the bronchial epithelial cells; (ii) Lad is tyrosine phosphorylated upon PDGF stimulation and is associated with PDGF receptor; (iii) upon PDGF stimulation, Grb2 is recruited to Lad in human embryonic lung cells; (iv) overexpression of Lad elevated AP-1 promoter activity by two- to threefold, whereas dominant negative Lad abrogated PDGF-dependent activation of AP-1 promoter. These results provide a novel mechanism of PDGF-dependent signaling, in which Lad acts as an adaptor in a tissue-specific manner, linking PDGF signal to Grb2 and subsequent activation of AP-1.
Copyright 2001 Academic Press.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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3T3 Cells
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Adaptor Proteins, Signal Transducing*
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Animals
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COS Cells
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Carrier Proteins / genetics
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Carrier Proteins / metabolism*
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Cell Line
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GRB2 Adaptor Protein
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Humans
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Lung / cytology
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Lung / drug effects
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Lung / metabolism*
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Mice
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Mice, Inbred C57BL
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Mutagenesis, Site-Directed
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Phosphorylation / drug effects
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Platelet-Derived Growth Factor / metabolism*
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Platelet-Derived Growth Factor / pharmacology
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Promoter Regions, Genetic
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Proteins / metabolism*
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RNA, Messenger / metabolism
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Receptors, Platelet-Derived Growth Factor / metabolism
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Signal Transduction / drug effects
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Signal Transduction / physiology*
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Transcription Factor AP-1 / genetics
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Transcription Factor AP-1 / metabolism
Substances
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Adaptor Proteins, Signal Transducing
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Carrier Proteins
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GRB2 Adaptor Protein
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GRB2 protein, human
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Grb2 protein, mouse
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Platelet-Derived Growth Factor
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Proteins
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RNA, Messenger
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Sh2d2a protein, mouse
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Transcription Factor AP-1
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Receptors, Platelet-Derived Growth Factor