| First Author | Gonzalez De La Cruz E | Year | 2022 |
| Journal | Int J Mol Sci | Volume | 23 |
| Issue | 15 | PubMed ID | 35897751 |
| Mgi Jnum | J:343023 | Mgi Id | MGI:7326372 |
| Doi | 10.3390/ijms23158175 | Citation | Gonzalez De La Cruz E, et al. (2022) MhcII Regulates Transmission of alpha-Synuclein-Seeded Pathology in Mice. Int J Mol Sci 23(15) |
| abstractText | MHCII molecules, expressed by professional antigen-presenting cells (APCs) such as T cells and B cells, are hypothesized to play a key role in the response of cellular immunity to alpha-synuclein (alpha-syn). However, the role of cellular immunity in the neuroanatomic transmission of alpha-syn pre-formed fibrillar (PFF) seeds is undetermined. To illuminate whether cellular immunity influences the transmission of alpha-syn seeds from the periphery into the CNS, we injected preformed alpha-syn PFFs in the hindlimb of the Line M83 transgenic mouse model of synucleinopathy lacking MhcII. We showed that a complete deficiency in MhcII accelerated the appearance of seeded alpha-syn pathology and shortened the lifespan of the PFF-seeded M83 mice. To characterize whether B-cell and T-cell inherent MhcII function underlies this accelerated response to PFF seeding, we next injected alpha-syn PFFs in Rag1-/- mice which completely lacked these mature lymphocytes. There was no alteration in the lifespan or burden of endstage alpha-syn pathology in the PFF-seeded, Rag1-deficient M83+/- mice. Together, these results suggested that MhcII function on immune cells other than these classical APCs is potentially involved in the propagation of alpha-syn in this model of experimental synucleinopathy. We focused on microglia next, finding that while microglial burden was significantly upregulated in PFF-seeded, MhcII-deficient mice relative to controls, the microglial activation marker Cd68 was reduced in these mice, suggesting that these microglia were not responsive. Additional analysis of the CNS showed the early appearance of the neurotoxic astrocyte A1 signature and the induction of the Ifngamma-inducible anti-viral response mediated by MhcI in the MhcII-deficient, PFF-seeded mice. Overall, our data suggest that the loss of MhcII function leads to a dysfunctional response in non-classical APCs and that this response could potentially play a role in determining PFF-induced pathology. Collectively, our results identify the critical role of MhcII function in synucleinopathies induced by alpha-syn prion seeds. |
