Background pattern of a brain with neural connections

Team De Camilli

Impaired integration of organelle function in Parkinson’s disease

2020-Present

We hypothesize that the functions of multiple Parkinson’s disease genes converge on common biochemical pathways involving endocytic organelles and/or mitochondria within vulnerable cell types. We will use a comprehensive cell biology tool kit including cutting-edge biochemistry, structural biology, microscopy at different scales, and genome editing tools to elucidate the function of selected Parkinson’s disease genes and the effects produced by their dysfunction both in cellular models in vitro and in mouse and rat models. By defining the molecular and cellular networks in which the products of these genes operate, we hope to identify strategies for reversing the cellular vulnerabilities that cause Parkinson’s disease or increase disease risk.

Tags
LRRK2 Lysosomal dysfunction Metabolism SYNJ1 VPS13C

Project Highlights

Contributions

Here is an overview of how this team’s article findings have contributed to the PD field as of June 2025. There are two different categorizations of these contributions – one by impact to the PD community and a second by scientific category.

Impact

Category

Accolades

Members of the team have been recognized for their contributions.

Team DeCamilli

Open Science Champions

De Camilli Lab, Ben Johnson

Network Spotlights

William Hancock-Cerutti

In the News

View All

Our Research Teams

Members of the CRN work diligently to advance our understanding of Parkinson’s disease. Learn more about recent CRN discoveries and achievements.