Neuronal mitochondria modulation of LPS-induced neuroinflammation Micah Harland, Sandy Torres, Jingyi Liu and Xinglong Wang Journal of Neuroscience 14 January 2020, 2324-19; DOI: https://doi.org/10.1523/JNEUROSCI.2324-19.2020
M Harland, etc
Journal of Neuroscience, 2020
Neuronal mitochondria dysfunction and neuroinflammation are two prominent pathological features increasingly realized as important pathogenic mechanisms for neurodegenerative diseases. However, little attempt has been taken to investigate the likely interactions between them. Mitofusin2 (Mfn2) is a mitochondrial outer membrane protein regulating mitochondrial fusion, a dynamic process essential for mitochondrial function. To explore the significance of neuronal mitochondria in the regulation of neuroinflammation, male and female transgenic mice with forced overexpression of Mfn2 specifically in neurons were intraperitoneally injected with lipopolysaccharide (LPS), a widely used approach to model neurodegeneration-associated neuroinflammation. Remarkably, LPS-induced lethality was almost completely abrogated in neuronal Mfn2 overexpression mice. Compared with non-transgenic wild type mice, mice with neuronal Mfn2 overexpression also exhibited alleviated body weight loss, behavioral sickness, and myocardial dysfunction. LPS-induced release of IL-1ß but not TNF-a was further found greatly inhibited in the central nervous system (CNS) of mice with neuronal Mfn2 overexpression, whereas peripheral inflammatory responses in the blood, heart, lung, and spleen remained unchanged. At the cellular and molecular levels, neuronal Mfn2 suppressed the activation of microglia, prevented LPS-induced mitochondrial fragmentation in neurons, and importantly, upregulated the expression of CX3CL1, a unique chemokine constitutively produced by neurons to suppress microglial activation. Together, these results reveal an unrecognized possible role of neuronal mitochondria in the regulation of microglial activation, and propose neuronal Mfn2 as a likely mechanistic linker between neuronal mitochondria dysfunction and neuroinflammation in neurodegeneration.