Detection of cleaved α-fodrin autoantigen in Sjögrenʹs syndrome: Apoptosis and co-localisation of cleaved α-fodrin with activated caspase-3 and cleaved poly(ADP-ribose) polymerase (PARP) in labial salivary glands

Summary nʹs syndrome (SS) is a systemic autoimmune disease which targets the exocrine glands and is associated with autoantibodies. The mechanism of salivary gland destruction or autoantibody production is poorly understood but it is increasingly accepted that apoptosis plays a role. ive jective of this study is to demonstrate the presence of cleaved α-fodrin autoantigen and apoptosis in the salivary glands of patients with primary Sjögrenʹs syndrome. s ients with primary Sjögrenʹs syndrome provided tissues from a labial salivary gland biopsy. Using terminal deoxynucleotidyl transferase mediated dUTP nick end labelling (TUNEL) assays to detect DNA fragmentation followed by sequential immunoperoxidase assays in the same patient biopsy to detect cleaved α-fodrin, Poly(ADP-ribose) polymerase (PARP), and caspase-3, we show a co-localisation between apoptotic markers and disease. s alisation of cleaved α-fodrin, PARP and caspase-3 expression was demonstrated primarily in the ducts along with DNA fragmentation in 16/18 salivary gland biopsies from Sjögrenʹs syndrome patients. None of these apoptotic markers was strongly expressed in healthy tissues. sion tic signals may provide useful therapeutic targets and cleaved α-fodrin may prove to be a marker of disease in primary Sjögrenʹs syndrome. Further studies are required to ascertain the specific association of cleaved α-fodrin with primary and secondary Sjögrenʹs syndrome.