Requirements for sulfate transport and the diastrophic dysplasia sulfate transporter in fibronectin matrix assembly.

Abstract

Diastrophic dysplasia sulfate transporter (DTDST) is a sulfate/chloride antiporter whose function is impaired in several human chondrodysplasias. We show that DTDST is upregulated by dexamethasone stimulation of HT1080 fibrosarcoma cells and is required for fibronectin (FN) extracellular matrix deposition by these cells. DTDST imports sulfate for the modification of glycosaminoglycans. We find that N-sulfation of these chains is important for FN matrix assembly and that sulfation of cell surface proteoglycans is reduced in the absence of DTDST. Of the candidate HT1080 cell surface proteoglycans, only loss of syndecan-2 compromises FN assembly, as shown by syndecan-2 small interfering RNA knockdown. DTDST is both necessary and sufficient to induce FN matrix assembly in HT1080 cells. Knockdown of DTDST ablates FN matrix, whereas its overexpression increases assembly without dexamethasone stimulation. These results identify a previously unrecognized regulatory pathway for matrix assembly via modulation of a sulfate transporter and proteoglycan sulfation. These data raise the possibility that FN assembly defects contribute to chondrodysplasias.

• Authors: Leontine L Galante, Jean E Schwarzbauer
• Journal: The Journal of cell biology (J Cell Biol) Vol. 179 Issue 5 Pg. 999-1009 (Dec 03 2007) ISSN: 1540-8140 [Electronic] United States
• PMID: 18056413 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)

Chemical References

• Anion Transport Proteins
• Fibronectins
• Glycosaminoglycans
• Membrane Transport Proteins
• Recombinant Fusion Proteins
• SLC26A2 protein, human
• Sulfate Transporters
• Sulfates
• Syndecan-2
• Dexamethasone

Topics

• Anion Transport Proteins (genetics, metabolism)
• Biological Transport (drug effects)
• Cell Line
• Cell Membrane (drug effects, metabolism)
• Dexamethasone (pharmacology)
• Extracellular Matrix (drug effects, metabolism)
• Fibronectins (metabolism)
• Glycosaminoglycans (metabolism)
• Humans
• Membrane Transport Proteins (genetics, metabolism)
• Protein Transport (drug effects)
• Recombinant Fusion Proteins (metabolism)
• Sulfate Transporters
• Sulfates (metabolism)
• Syndecan-2 (deficiency)
• Up-Regulation (drug effects)