AIMS: Peroxidases serve diverse biological functions including well-characterized activities in host defence and hormone biosynthesis. More recently, peroxidasin (PXDN) was found to be involved in collagen IV cross-linking in the extracellular matrix (ECM). The aim of this study was to characterize the expression and function of peroxidasin-like protein (PXDNL), a previously unknown peroxidase homologue. METHODS AND RESULTS: We cloned the PXDNL cDNA from the human heart and identified its expression pattern by northern blot, in situ hybridization, and immunohistochemistry. PXDNL is expressed exclusively in the heart and it has evolved to lose its peroxidase activity. The protein is produced by cardiomyocytes and localizes to cell-cell junctions. We also demonstrate that PXDNL can form a complex with PXDN and antagonizes its peroxidase activity. Furthermore, we show an increased expression of PXDNL in the failing myocardium. CONCLUSION: PXDNL is a unique component of the heart with a recently evolved inactivation of peroxidase function. The elevation of PXDNL levels in the failing heart may contribute to ECM dysregulation due to its antagonism of PXDN function.
AIMS: Peroxidases serve diverse biological functions including well-characterized activities in host defence and hormone biosynthesis. More recently, peroxidasin (PXDN) was found to be involved in collagen IV cross-linking in the extracellular matrix (ECM). The aim of this study was to characterize the expression and function of peroxidasin-like protein (PXDNL), a previously unknown peroxidase homologue. METHODS AND RESULTS: We cloned the PXDNL cDNA from the human heart and identified its expression pattern by northern blot, in situ hybridization, and immunohistochemistry. PXDNL is expressed exclusively in the heart and it has evolved to lose its peroxidase activity. The protein is produced by cardiomyocytes and localizes to cell-cell junctions. We also demonstrate that PXDNL can form a complex with PXDN and antagonizes its peroxidase activity. Furthermore, we show an increased expression of PXDNL in the failing myocardium. CONCLUSION:PXDNL is a unique component of the heart with a recently evolved inactivation of peroxidase function. The elevation of PXDNL levels in the failing heart may contribute to ECM dysregulation due to its antagonism of PXDN function.
Entities:
Keywords:
Extracellular matrix; Peroxidase; Peroxidasin; Peroxidasin-like protein; Reactive oxygen species
Authors: Monika Soudi; Martina Paumann-Page; Cedric Delporte; Katharina F Pirker; Marzia Bellei; Eva Edenhofer; Gerhard Stadlmayr; Gianantonio Battistuzzi; Karim Zouaoui Boudjeltia; Paul G Furtmüller; Pierre Van Antwerpen; Christian Obinger Journal: J Biol Chem Date: 2015-02-24 Impact factor: 5.157
Authors: Hector Barajas-Martinez; Maya Smith; Dan Hu; Robert J Goodrow; Colleen Puleo; Can Hasdemir; Charles Antzelevitch; Ryan Pfeiffer; Jacqueline A Treat; Jonathan M Cordeiro Journal: Stem Cells Int Date: 2020-09-01 Impact factor: 5.443
Authors: Jacqueline A Treat; Ryan Pfeiffer; Hector Barajas-Martinez; Robert J Goodrow; Corina Bot; Rodolfo J Haedo; Ronald Knox; Jonathan M Cordeiro Journal: Int J Mol Sci Date: 2021-07-01 Impact factor: 5.923