Search bioRxiv⌕ Search

Biology subjects

Lordkipanidze, M.

Publications and source records attributed to Lordkipanidze, M..

2 recordsLinked to original sources

cGAS integrates Toll-like receptor signaling in platelets to promote thromboinflammation

Thromboinflammation is driven by innate immune signaling and promotes tissue injury during sepsis. Activation of platelets by bacterial products and alarmins amplifies inflammation, coagulation, and thrombotic dysfunction. However, the mechanisms by which these diverse inflammatory signals converge to elicit common platelet responses remain largely undefined. Mitochondria are key integrators of cellular stress responses and can activate innate immune pathways through the release of mitochondrial DNA and engagement of the DNA sensor cGAS. We therefore hypothesized that stimulation of innate immune receptors generates endogenous cGAS ligands within platelets, providing a unifying mechanism by which distinct inflammatory cues converge on cGAS-STING signaling. Here, we demonstrate that activation of TLR4, TLR1/2, and TLR5 engages a platelet-intrinsic mtDNA-cGAS-STING axis that promotes platelet activation. In a model of endotoxemia, genetic deletion of cGAS reduced platelet activation, thrombocytopenia, pyroptosis and the early systemic inflammatory response. Platelet transfer experiments further established that platelet-intrinsic cGAS is sufficient to amplify inflammatory responses in vivo. Mechanistically, we demonstrated that cytosolic accumulation of mtDNA and activation of cGAS-STING signaling pathway in platelets are dependent on mitochondrial calcium uniporter (MCU) and correlated with the loss of mitochondrial membrane potential and the production of mitochondrial reactive oxygen species. In contrast, canonical platelet agonists activated platelets independently of cGAS and failed to induce substantial cytosolic mtDNA accumulation. Importantly, this signaling architecture was conserved in human platelets, where TLR1/2-mediated activation required MCU- and STING-dependent signaling, whereas responses to thrombin receptor-activating peptide and collagen-related peptide remained largely unaffected. Together, these findings identify cGAS as an intracellular signal integration node that allows diverse innate immune receptors to converge on a common platelet activation pathway through sensing of mitochondria-derived DNA, allowing a rapid platelet response to microbial products.

cell biology↗

Differential Correlation of Serum BDNF and microRNA Content in Rats with Rapid or Late Onset of Heavy Alcohol Use

Heavy alcohol use reduces the levels of the brain-derived neurotrophic factor (BDNF) in the prefrontal cortex of rodents through the upregulation of microRNAs targeting BDNF mRNA. In humans, an inverse correlation exists between circulating blood levels of BDNF and the severity of psychiatric disorders including alcohol abuse. Here, we set out to determine whether a history of heavy alcohol use produces comparable alterations in the blood of rats. We used an intermittent access to 20% alcohol using the 2-bottle choice paradigm (IA20%2BC), and measured circulating levels of BDNF protein and microRNAs in the serum of Long-Evans rats before and after 8-weeks of excessive alcohol intake. We observed that the drinking profile of heavy alcohol users is not unified; Whereas 70% of the rats gradually escalate their alcohol intake (Late Onset), 30% of alcohol users exhibit a very Rapid Onset of drinking (Rapid Onset). We found that serum BDNF levels are negatively correlated with alcohol intake in both Rapid Onset and Late Onset rats. In contrast, increased expression of the microRNAs (miRs) targeting BDNF, miR30a-5p, miR-195-5p, miR191-5p and miR206-3p, was detected only in the Rapid Onset rats. Finally, we report that the alcohol-dependent molecular changes are not due to alterations in platelet number. Our data suggest that rats exhibit both Late and Rapid Onset of alcohol intake. We further show that heavy alcohol use produces comparable changes in BDNF protein levels in both groups. However, circulating microRNAs are responsive to alcohol only in the Rapid Onset rats.

neuroscience↗