PINK1 deficiency rewires early immune responses in a mouse model of Parkinson's disease triggered by intestinal infection

PINK1 缺陷会重塑由肠道感染诱发的帕金森病小鼠模型中的早期免疫反应。

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作者:Sherilyn Junelle Recinto ,Alexandra Kazanova ,Lin Liu ,Brendan Cordeiro ,Shobina Premachandran ,Hicham Bessaiah ,Alexis Allot ,Elia Afanasiev ,Sriparna Mukherjee ,Jessica Pei ,Adam MacDonald ,Moein Yaqubi ,Heidi M McBride ,Diana Matheoud ,Louis-Eric Trudeau ,Samantha Gruenheid ,Jo Anne Stratton

Abstract

Parkinson's disease is characterized by a period of non-motor symptoms, including gastrointestinal dysfunction, preceding motor deficits by several years to decades. This long prodrome is suggestive of peripheral immunity involvement in the initiation of disease. We previously developed a model system in PINK1 KO mice displaying PD-like motor symptoms at late stages following intestinal infections. Herein, we map the initiating immune events at the site of infection in this model. Using single-cell RNAseq, we demonstrate that peripheral myeloid cells are the earliest highly dysregulated immune cell type followed by an aberrant T cell response shortly after. We also demonstrate an increased propensity for antigen presentation and that activated myeloid cells acquire a proinflammatory profile capable of inducing cytotoxic T cell responses. Together, our study provides the first evidence that PINK1 is a key regulator of immune functions in the gut underlying early PD-related disease mechanisms.

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