Abstract

IntroductionOur understanding of autoimmunity is skewed considerably towards the late stages of overt disease and chronic inflammation. Defining the targeted organ’s role during emergence of autoimmune diseases is, however, critical in order to define their etiology, early and covert disease phases and delineate their molecular basis.MethodsUsing Sjögren’s syndrome (SS) as an exemplary rheumatic autoimmune disease and temporal global gene-expression profiling, we systematically mapped the transcriptional landscapes and chronological interrelationships between biological themes involving the salivary glands’ extracellular milieu. The time period studied spans from pre- to subclinical and ultimately to onset of overt disease in a well-defined model of spontaneous SS, the C57BL/6.NOD-Aec1Aec2 strain. In order to answer this aim of great generality, we developed a novel bioinformatics-based approach, which integrates comprehensive data analysis and visualization within interactive networks. The latter are computed by projecting the datasets as a whole on a priori-defined consensus-based knowledge.ResultsApplying these methodologies revealed extensive susceptibility loci-dependent aberrations in salivary gland homeostasis and integrity preceding onset of overt disease by a considerable amount of time. These alterations coincided with innate immune responses depending predominantly on genes located outside of the SS-predisposing loci Aec1 and Aec2. Following a period of transcriptional stability, networks mapping the onset of overt SS displayed, in addition to natural killer, T- and B-cell-specific gene patterns, significant reversals of focal adhesion, cell-cell junctions and neurotransmitter receptor-associated alterations that had prior characterized progression from pre- to subclinical disease.ConclusionsThis data-driven methodology advances unbiased assessment of global datasets an allowed comprehensive interpretation of complex alterations in biological states. Its application delineated a major involvement of the targeted organ during the emergence of experimental SS.

Highlights

  • Our understanding of autoimmunity is skewed considerably towards the late stages of overt disease and chronic inflammation

  • Extent of alterations across the three time periods Application of the data analysis pipeline outlined in Figure 1 revealed that the most thematically diverse alterations specific for C57BL/6.NOD-Aec1Aec2 mice, involving the most extracellular milieu (EM)-related gene set (GS) and EM-associated GSs (Figure 2B), occurred between 4 and 8 weeks of age

  • The same was true for the number of genes accounting for the GSs’ significant enrichment or depletion, that is, leading edge (LE) genes (Figures 2C and 2D)

Read more

Summary

Introduction

Our understanding of autoimmunity is skewed considerably towards the late stages of overt disease and chronic inflammation. To a certain extent stratify, the molecular events associated with subclinical phases of autoimmune diseases is the use of adequate experimental models [6,7]. For this purpose, a suitable experimental strain must, in correspondence with humans, develop its relevant autoimmune phenotype over an extended period of time and in the context of its genetic background. Studies designed to discover genetic associations have focused either on innate immunity [12] or on genes that might explain the dominant role of B cells in the pathogenesis of SS [10] These studies have yet to yield results that allow estimation of an individual’s risk of developing SS

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.