Protocols for Recinto et al. "PINK1 deficiency rewires early immune responses in a mouse model of Parkinson’s disease triggered by intestinal infection" V.3
Collection Citation: Sherilyn Junelle Recinto, Adam MacDonald, Moein Yaqubi, Alexandra Kazanova 2025. Protocols for Recinto et al. "PINK1 deficiency rewires early immune responses in a mouse model of Parkinson’s disease triggered by intestinal infection". protocols.io https://dx.doi.org/10.17504/protocols.io.kxygxy77ol8j/v3Version created by Lilia Rodriguez
License: This is an open access collection distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
We use this collection and it's working
Created: April 30, 2025
Last Modified: April 30, 2025
Collection Integer ID: 204072
Keywords: ASAPCRN, immune cell type in pink1 ko, early immune response, initiating immune event, dysregulated immune cell type, immune events at the site, targeted pathogen, induced pd mouse modeling system, pink1 ko mice with gram, cell interaction pathway, pink1 ko mice, enhanced proinflammatory profile, myeloid cell, infection at the earliest stage, pd mouse modeling system, mouse model, mice, antigen presentation, proinflammatory profile, cell
Funders Acknowledgements:
Aligning Science Across Parkinson's
Grant ID: ASAP-000525
Disclaimer
The protocols.io team notes that research involving animals and humans must be conducted according to internationally-accepted standards and should always have prior approval from an Institutional Ethics Committee or Board.
Abstract
Our group has developed GI-targeted pathogen-induced PD mouse modeling systems (in PINK1 KO mice with gram negative bacterial infections) and found that T cells are a major player in driving PD-like motor symptoms at late stages following infection. Herein, we now map the initiating immune events at the site of infection at the earliest stages with the goal of shedding light on the earliest mechanisms triggering T cell-mediated pathological processes relevant to PD. Using unbiased single cell sequencing, we demonstrate that myeloid cells are the earliest dysregulated immune cell type in PINK1 KO infected mice (at 1-week post-infection) followed by a dysregulated T cell response shortly after (at 2 weeks post-infection). We find that these myeloid cells have an enhanced proinflammatory profile, are more mature, and develop enhanced capacity for antigen presentation. Using unbiased prediction analysis, our data suggests that cytotoxic T cells and myeloid cells are particularly poised for interacting with each other, and we identify possible direct cell-cell interaction pathways that might be implicated.
Disclaimer
The protocols.io team notes that research involving animals and humans must be conducted according to internationally-accepted standards and should always have prior approval from an Institutional Ethics Committee or Board.
