Neuroimmune signaling by extracellular vesicles

Systemic inflammation has a strong impact on brain function and contributes to the immediate and long-term development of various pathologies. The classic view is that a systemic inflammation influences the brain via the release of inflammatory cytokines (e.g. IL-1ß, IL6, TNFα), which in turn activate microglia directly or via endothelial cells but may also act on neurons. As a neural mechanism, cytokines may activate the vagus nerve within the abdominal and thoracic cavity by relaying a signal to neuronal populations in the brainstem. Lately, other nonclassical ways of spreading disease from the periphery to the brain with a link to inflammation have been suggested, particularly for Parkinson’s disease, but the nature of the responsible agent remains unclear. In the light of this latter concept, it is particularly interesting that we were recently able to identify the direct transfer of functional RNA from peripheral blood to neurons via extracellular vesicles [1]. Extracellular vesicles (EVs) are a heterogeneous population of small, membrane-bound particles containing multiple types of molecules such as lipids, ribonucleotides and proteins. It has been postulated that EVs are important regulators of the immune response [2], but most data are based on in vitro experiments or studies involving at least some in vitro manipulations, thereby questioning their physiological relevance. In contrast, for the first time we were able to demonstrate a transfer of functional RNA by EVs in vivo. This was achieved by using the Cre/LoxP system to visualize the contribution of blood cells to other organs, originally in the context of cell fusion (Figure 1) [3]. Briefly, expression of Cre recombinase specifically in blood cells leads to the release of Cre mRNA via EVs into the circulation that can then reach neurons in the brain, but only after peripheral inflammation. While we detect changes in the miRNA composition of EVs receiving neurons, currently we do not know whether this process is pathologic or acts as a rescue mechanism, trying to counteract cellular stress induced by yet other molecules. Also, the specificity of the response remains unclear, although our data suggest that the local permeability of the blood-brain barrier is a likely parameter. In general, the visualization of RNA transfer by EVs in vivo will allow the identification of routes of communication between distant cells, which was previously not possible, and we could confirm the validity of our approach by giving the first account of tumor-tohost signaling [4]. Of particular interest in the light of our findings of a route from immune cells to the brain is the fact that the main target of malignant astrocytoma EVs appears to be immune cells infiltrating into the tumor mass. This could indicate the general possibility of a reverse information transfer from the brain to the immune Editorial