ADAMTS-10 and -6 differentially regulate cell-cell junctions and focal adhesions

• Published in: Scientific reports Vol. 6; no. 1; p. 35956
• Main Authors: Cain, Stuart A., Mularczyk, Ewa J., Singh, Mukti, Massam-Wu, Teresa, Kielty, Cay M.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 25-10-2016; Nature Publishing Group
• Subjects: 14; 14/28; 14/63; 38; 38/39; 631/337/505; 631/80/79/2027; 631/80/79/2028; 631/80/79/750; 82; 82/103; 82/80; Active sites; ADAMTS Proteins - genetics; ADAMTS Proteins - metabolism; Cell junctions; DNA Mutational Analysis; Enzymatic activity; Epithelial Cells - physiology; Fibrillin; Fibronectin; Focal Adhesions; Furin; Gene Expression; Gene Knockdown Techniques; Heparan sulfate; Heparin; Humanities and Social Sciences; Humans; Intercellular Junctions; Interfaces; multidisciplinary; Mutagenesis; Mutation; Overexpression; Science; siRNA; Sulfates; Syndecan
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/srep35956

ADAMTS10 and ADAMTS6 are homologous metalloproteinases with ill-defined roles. ADAMTS10 mutations cause Weill-Marchesani syndrome (WMS), implicating it in fibrillin microfibril biology since some fibrillin-1 mutations also cause WMS. However little is known about ADAMTS6 function. ADAMTS10 is resistant to furin cleavage, however we show that ADAMTS6 is effectively processed and active. Using siRNA, over-expression and mutagenesis, it was found ADAMTS6 inhibits and ADAMTS10 is required for focal adhesions, epithelial cell-cell junction formation, and microfibril deposition. Either knockdown of ADAMTS6, or disruption of its furin processing or catalytic sites restores focal adhesions, implicating its enzyme activity acts on targets in the focal adhesion complex. In ADAMTS10-depleted cultures, expression of syndecan-4 rescues focal adhesions and cell-cell junctions. Recombinant C-termini of ADAMTS10 and ADAMTS6, both of which induce focal adhesions, bind heparin and syndecan-4. However, cells overexpressing full-length ADAMTS6 lack heparan sulphate and focal adhesions, whilst depletion of ADAMTS6 induces a prominent glycocalyx. Thus ADAMTS10 and ADAMTS6 oppositely affect heparan sulphate-rich interfaces including focal adhesions. We previously showed that microfibril deposition requires fibronectin-induced focal adhesions, and cell-cell junctions in epithelial cultures. Here we reveal that ADAMTS6 causes a reduction in heparan sulphate-rich interfaces, and its expression is regulated by ADAMTS10.