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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2006-11-22
pubmed:abstractText
Integrin alpha3beta1 is a receptor for the extracellular matrix component laminin 5. To elucidate possible signaling pathways induced by integrin alpha3beta1, we looked for proteins that interact with the cytoplasmic part of the alpha3A integrin subunit. We identified several multifunctional proteins by affinity chromatography and subsequent MALDI-TOF-MS and focused on the inhibitor 1 of serine/threonine phosphatase PP2A (I1PP2A, synonym: lanp) which also plays a role during the development of the mouse cerebellum. I1PP2A/lanp colocalizes with the alpha3A integrin subunit in differentiated PC12 cells in the cell body and in neurites as well as in Purkinje cells of mouse cerebellum. Overexpression of GFP-I1PP2A/lanp in PC12 cells leads to markedly reduced neurite length on laminin 5 after induction with nerve growth factor. By affinity chromatography the protein phosphatase PP1 can also be identified as a alpha3A/cyto-binding protein. PP1 and integrin alpha3beta1 can be pulled down by GST-I1PP2A/lanp from cell lysates of differentiated and undifferentiated PC12 cells. The phosphatase binds to the cytoplasmic membrane-proximal conserved GFFKR motif of the alpha integrin subunit, whereas I1PP2A/lanp requires a longer sequence for binding. PP1 but not PP2A is able to dephosphorylate precipitated integrin alpha3beta1 in vitro. Furthermore, PP1 releases phosphate from T1046 of phosphopeptides that mimic the phosphorylation consensus sequence in the cytoplasmic part of the alpha3A integrin subunit. These data suggest that I1PP2A/lanp forms a complex with PP1 and the alpha3A integrin subunit and might possibly regulate the phosphorylation status of integrin alpha3beta1 and/or integrin downstream targets.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Atrial Natriuretic Factor, http://linkedlifedata.com/resource/pubmed/chemical/Calcium-Binding Protein, Vitamin..., http://linkedlifedata.com/resource/pubmed/chemical/Green Fluorescent Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Integrin alpha3beta1, http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments, http://linkedlifedata.com/resource/pubmed/chemical/Phosphoric Monoester Hydrolases, http://linkedlifedata.com/resource/pubmed/chemical/Potassium Chloride, http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins, http://linkedlifedata.com/resource/pubmed/chemical/atrial natriuretic factor..., http://linkedlifedata.com/resource/pubmed/chemical/calbindin, http://linkedlifedata.com/resource/pubmed/chemical/polyphosphoinositide phosphatase
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0360-4012
pubmed:author
pubmed:issnType
Print
pubmed:volume
84
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1759-70
pubmed:meshHeading
pubmed-meshheading:17016859-Animals, pubmed-meshheading:17016859-Atrial Natriuretic Factor, pubmed-meshheading:17016859-Blotting, Western, pubmed-meshheading:17016859-Calcium-Binding Protein, Vitamin D-Dependent, pubmed-meshheading:17016859-Cell Differentiation, pubmed-meshheading:17016859-Chromatography, Affinity, pubmed-meshheading:17016859-Gene Expression, pubmed-meshheading:17016859-Green Fluorescent Proteins, pubmed-meshheading:17016859-Immunohistochemistry, pubmed-meshheading:17016859-Integrin alpha3beta1, pubmed-meshheading:17016859-Neurites, pubmed-meshheading:17016859-PC12 Cells, pubmed-meshheading:17016859-Peptide Fragments, pubmed-meshheading:17016859-Peptide Mapping, pubmed-meshheading:17016859-Phosphoric Monoester Hydrolases, pubmed-meshheading:17016859-Potassium Chloride, pubmed-meshheading:17016859-Protein Binding, pubmed-meshheading:17016859-Rats, pubmed-meshheading:17016859-Recombinant Fusion Proteins, pubmed-meshheading:17016859-Transfection
pubmed:year
2006
pubmed:articleTitle
Integrin alpha3beta1 interacts with I1PP2A/lanp and phosphatase PP1.
pubmed:affiliation
Institut für Molekularbiologie und Biochemie, Charité-Universitätsmedizin Berlin, Campus Benjamin Franklin, Berlin-Dahlem, Germany.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't