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1.
J Cell Physiol ; 229(10): 1538-47, 2014 Oct.
Article in English | MEDLINE | ID: mdl-24585683

ABSTRACT

Expression studies have implicated FLRT2 in cranial neural crest cell migration and prechondrogenic cell condensation during craniofacial skeletogenesis. We aimed to determine whether FLRT2 was involved in mediating cell-matrix interactions in the ATDC5 chondroprogenitor cell line. Immunolocalization experiments of ATDC5 cells revealed that FLRT2 was present on the cell membrane as well as extracellularly, where it colocalized with Fibronectin (Fn). After cell extraction of the matrix, FLRT2 was identified in the ATDC5-derived extracellular matrix (ECM) and was further found to be associated with Fn-coated beads in cell cultures. Blockage of Fn fibril formation via a blocking peptide resulted in a concomitant decrease in extracellular FLRT2 accumulation. Over a 7-day period following the replenishment of the Fn blocking peptide to the cultures, there was a partial rebound in Fn fibril formation that was accompanied by a concomitant reappearance of FLRT2 co-expression. Co-immunoprecipitation confirmed that FLRT2 and Fn interacted, either directly or indirectly. Immunoprecipitation and Western blot analyses with antibodies recognizing epitopes located on the extra- and intracellular domains of FLRT2 further revealed the presence of different sized bands, suggesting that FLRT2 may exist in both membrane-bound and shed forms. Our data therefore provide evidence that FLRT2 and/or its cleavage products may be cooperating with Fn and other ECM proteins to regulate critical cellular events. Further studies will be necessary in delineate more precisely the roles of FLRT2 in mediating cell- and cell-matrix interactions during normal development.


Subject(s)
Chondrocytes/metabolism , Fibronectins/metabolism , Membrane Glycoproteins/metabolism , Stem Cells/metabolism , Animals , Blotting, Western , Cell Line , Cell Membrane/metabolism , Chondrogenesis , Extracellular Matrix/metabolism , Immunoprecipitation , Mice , Molecular Weight , Peptide Fragments/metabolism , Protein Binding , Time Factors
4.
Hum Genet ; 121(2): 287, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17354001
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