Defective signalling in salivary glands precedes the autoimmune response in the non-obese diabetic mouse model of sialadenitis

The spontaneous non-obese diabetic (NOD) mouse model of Sjögren's syndrome provides a valuable tool to study the onset and progression of both the autoimmune response and secretory dysfunction. Our purpose was to analyse the temporal decline of salivary secretion in NOD mice in relation to the...

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Detalhes bibliográficos
Autores: Rosignoli, F., Roca, V., Meiss, R., Leceta, J., Gomariz, R.P., Leirós, C.P.
Tipo de documento: artigo
Estado:Versão publicada
Data de publicação:2005
País:Argentina
Recursos:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
Repositório:Biblioteca Digital (UBA-FCEN)
Idioma:inglês
OAI Identifier:paperaa:paper_00099104_v142_n3_p411_Rosignoli
Acesso em linha:http://hdl.handle.net/20.500.12110/paper_00099104_v142_n3_p411_Rosignoli
Access Level:Acceso aberto
Palavra-chave:Autoimmune response
Nitric oxide signalling
NOD mice
Sialadenitis
Sjögren's syndrome
cyclic AMP
cyclic GMP
neurotransmitter
nitric oxide
nitric oxide synthase
vasoactive intestinal polypeptide
animal experiment
animal model
animal tissue
article
autoimmunity
cell infiltration
cytokine production
enzyme activity
female
immune response
mononuclear cell
mouse
mouse strain
nonhuman
parotid gland
priority journal
salivary gland
salivation
sialoadenitis
signal transduction
Sjoegren syndrome
submandibular gland
Animals
Autoantibodies
Autoimmunity
Cyclic GMP
Cytokines
Diabetes Mellitus, Type 1
Disease Models, Animal
Female
Mice
Mice, Inbred BALB C
Mice, Inbred NOD
Nitric Oxide Synthase
Parotid Gland
Salivary Glands
Signal Transduction
Submandibular Gland
Vasoactive Intestinal Peptide
Descrição
Resumo:The spontaneous non-obese diabetic (NOD) mouse model of Sjögren's syndrome provides a valuable tool to study the onset and progression of both the autoimmune response and secretory dysfunction. Our purpose was to analyse the temporal decline of salivary secretion in NOD mice in relation to the autoimmune response and alterations in various signalling pathways involved in saliva secretion within each salivary gland. A progressive loss of nitric oxide synthase activity in submandibular and parotid glands started at 12 weeks of age and paralleled the decline in salivary secretion. This defect was associated with a lower response to vasoactive intestinal peptide in salivary flow rate, cAMP and nitric oxide/cGMP production. No signs of mononuclear infiltrates or local cytokine production were detectable in salivary glands in the time period studied (10-16 weeks of age). Our data support a disease model for sialadenitis in NOD mice in which the early stages are characterized by defective neurotransmitter-mediated signalling in major salivary glands that precedes the autoimmune response. © 2005 British Society for Immunology.