TREM2 Alzheimer’s variant R47H causes similar transcriptional dysregulation to knockout, yet only subtle functional phenotypes in human iPSC-derived macrophages

<p><strong>Background:</strong><br /> TREM2 is a microglial cell surface receptor, with risk mutations linked to Alzheimer’s disease (AD), including R47H. TREM2 signalling via SYK aids phagocytosis, chemotaxis, survival, and changes to microglial activation state. In AD mouse...

Full description

Bibliographic Details
Main Authors: Hall-Roberts, H, Di Daniel, E, Agarwal, D, Obst, J, Smith, TB, Monzón-Sandoval, J, Webber, C, James, WS, Mead, E, Davis, JB, Cowley, SA
Format: Journal article
Language:English
Published: BioMed Central 2020