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Cystic Fibrosis Transmembrane Conductance Regulator Can Export Hyaluronan
Author(s) -
Tobias Schulz,
Udo Schumacher,
Christian Prante,
Wolfgang Sextro,
Peter Prehm
Publication year - 2010
Publication title -
pathobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.941
H-Index - 53
eISSN - 1423-0291
pISSN - 1015-2008
DOI - 10.1159/000295859
Subject(s) - cystic fibrosis transmembrane conductance regulator , cystic fibrosis , extracellular matrix , transporter , chemistry , fibroblast , downregulation and upregulation , δf508 , atp binding cassette transporter , microbiology and biotechnology , cell culture , biology , medicine , biochemistry , in vitro , gene , genetics
Hyaluronan, a major water binding component of the extracellular matrix, is synthesised within the cytosol and exported across the plasma membrane by the ABC-transporter MRP5 in fibroblasts. Although its synthesis is vital for embryogenesis, MRP5-deficient mice are without phenotype, suggesting that another transporter had substituted for the MRP5 protein. Thus, we searched for a compensatory exporter in fibroblasts from MRP5 deficient mice and found that cystic fibrosis transmembrane conductance regulator (CFTR) mRNA was upregulated.

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