Evidence obtained with the nonobese diabetic Sjgrens mouse model also supports this view provid ing a feasible approach for this search. The NOD mouse model of Sjgrens syndrome, at the pre diabetic stage, has the unique characteristic of developing a deep secretory dys function with mild infiltration of the glands consistent with a structural dysfunctional aetiology. The role of apoptosis of secretory epithelium as a triggering factor of early dysfunction and autoimmune response has been explored in patients with Sjgrens syndrome and in the pre diabetic NOD mouse model. Apoptosis evaluated by ter minal UTP nucleotide end labelling method and Fas FasL mediated apoptosis have already been reported in both cases.
In keeping with this, we have shown early sig nalling alterations in submandibular glands from NOD mice involving neural isoform of nitric oxide synthase, cal cium selleck chemical Microtubule Inhibitor calmodulin kinase II and cGMP. Moreover, with a lower activity of NOS 1 in exocrine glands and higher serum levels of TNF , we recently reported an increased DNA frag mentation with increased Bax expression in isolated acinar cells from NOD submandibular glands at the Sjgrens syn drome like period. TNF and TNF receptors are important cell surface inducers of apoptosis leading to proteolysis and DNA fragmentation. The ability of TNF to regulate apoptosis in isolated pancreatic acini and experi mental pancreatitis has previously been reported. Vasoactive intestinal peptide is a neuroimmunopeptide with several actions on exocrine glands.
In addition to inducing vasodilation and exocrine secretion, VIP was postulated as a trophic factor for acini and it has shown strong anti inflam matory properties in several models of chronic autoimmune and immune mediated inflammatory diseases . Regarding NOD mice at the Sjgrens syndrome like stage, treatment with VIP in vivo from the fourth selelck kinase inhibitor week of age reduced Th1 cytokine levels in the serum and increased IL 10. In line with this, VIP was proposed as one of the promising approaches for the treatment of Sjgrens syndrome based on VIP gene transfer experiments in NOD females. The aim of the present study was to analyse apoptotic events involving TNF TNF R in isolated acini from NOD mice sub mandibular glands and to explore the ability of VIP to modulate these effects. In addition to Bax and other pro apoptotic and anti apoptotic signals, we investigated the expression of two proteins encoded by tumour protein 53 induced nuclear pro tein 1 gene, TP53INP1 and whose over expression was associated to Bax expression and apoptosis. Our present data indicate that isolated acini from sub mandibular glands of NOD mice present increased chromatin condensation, TNF R, Bax and TP53INP1 expression, and caspase 3 activity than normal BALBc mice.