Alteration of Mitochondrial DNA Copy Number and Increased Expression Levels of Mitochondrial Dynamics-Related Genes in Sjögren’s Syndrome
2022
Giada De Benedittis | Andrea Latini | Serena Colafrancesco | Roberta Priori | Carlo Perricone | Lucia Novelli | Paola Borgiani | Cinzia Ciccacci
Sjögren’s syndrome (SS) is a chronic autoimmune multifactorial disease characterized by inflammation and lymphocytic infiltration of the exocrine glands. Several studies have highlighted the involvement of oxidative stress in this pathology, suggesting that it could induce mitochondrial dysfunctions. Mitochondria could have a role in inflammatory and immune processes. Since the mitochondrial DNA (mtDNA) copy number could change in response to physiological or environmental stimuli, this study aimed to evaluate possible alterations in the mtDNA copy number in SS. We have analyzed the amount of mtDNA in the peripheral blood of 74 SS patients and 61 healthy controls by qPCR. Then, since mitochondrial fusion and fission play a crucial role in maintaining the number of mitochondria, we investigated the expression variability of the genes most commonly involved in mitochondrial dynamics in a subgroup of SS patients and healthy controls. Interestingly, we observed a highly significant decrease in mtDNA copies in the SS patients compared to healthy controls (<i>p</i> = 1.44 × 10<sup>−12</sup>). Expression levels of mitochondrial fission factor (<i>MFF</i>), mitofusin-1 (<i>MFN1</i>), and mitochondrial transcription factor A (<i>TFAM</i>) genes were analyzed, showing a statistically significant increase in the expression of <i>MFF</i> (<i>p</i> = 0.003) and <i>TFAM</i> (<i>p</i> = 0.022) in the SS patients compared to healthy controls. These results give further insight into the possible involvement of mitochondrial dysfunctions in SS disease.
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