Research demonstrates the expression of key molecules in the anti-inflammatory cholinergic pathway, suggesting extrasplenic signaling mechanisms.
The anti-inflammatory cholinergic pathway describes the interaction between cholinergic vagal nerves and splenic immune cells, yet the exact mechanisms underlying the anti-inflammatory cholinergic pathway remain disputed. Here, we mapped the expression of key molecular components of the anti-inflammatory cholinergic pathway in the adult mouse using RNAScope in situ hybridization (ISH) and quantitative PCR (qPCR). In C57BL/6J wild-type male mice, we observed the expression of choline acetyltransferase ( Chat ) and alpha 7 nicotinic acetylcholine receptor ( Chrna7 ) in various autonomic neurons throughout the body, but not in the spleen, even after bacterial lipopolysaccharide (LPS) treatment. In contrast, the beta-2 adrenergic receptor ( Adrb2 ), another autonomic receptor with well-documented anti-inflammatory actions, was highly expressed in the spleen, with a significant decrease following LPS administration. Interestingly, Adrb2 was also expressed at lower levels in the spleen of a newly generated global knockout mouse for Chrna7 . Lastly, we did not observe YFP-positive cells or axons in the spleen of the ChAT-Cre-ChR2-YFP mouse. Based on our findings, we propose a new model of the cholinergic anti-inflammatory pathway that highlights the roles of extrasplenic cholinergic signaling.
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Merchant et al. (2025) studied this question.
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