Droplet-based forward genetic screening of astrocyte–microglia cross-talk

Michael A. Wheeler(Broad Institute), Iain C. Clark(QB3), Hong‐Gyun Lee(Brigham and Women's Hospital), Zhaorong Li(Broad Institute), Mathias Linnerbauer(Brigham and Women's Hospital), Joseph M. Rone(Brigham and Women's Hospital), Manon Blain(Montreal Neurological Institute and Hospital), Camilo Faust Akl(Brigham and Women's Hospital), Gavin Piester(Brigham and Women's Hospital), Federico Giovannoni(Brigham and Women's Hospital), Marc Charabati(Brigham and Women's Hospital), Joon-Hyuk Lee(Brigham and Women's Hospital), Yoon-Chul Kye(Brigham and Women's Hospital), Joshua Choi(Brigham and Women's Hospital), Liliana M. Sanmarco(Brigham and Women's Hospital), Léna Srun(Brigham and Women's Hospital), Elizabeth N Chung(Brigham and Women's Hospital), Lucas E. Flausino(Brigham and Women's Hospital), Brian M. Andersen(Brigham and Women's Hospital), Veit Rothhammer(Brigham and Women's Hospital), Hiroshi Yano(Cornell University), Tomer Illouz(Brigham and Women's Hospital), Stéphanie Zandee(Centre Hospitalier de l’Université de Montréal), Carolin Daniel(Helmholtz Zentrum München), David Artis(Cornell University), Marco Prinz(University of Freiburg), Adam R. Abate(QB3), Vijay K. Kuchroo(Broad Institute), Jack P. Antel(Montreal Neurological Institute and Hospital), Alexandre Prat(Centre Hospitalier de l’Université de Montréal), Francisco J. Quintana(Broad Institute)
Science
March 10, 2023
Cited by 115Open Access
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Abstract

Cell-cell interactions in the central nervous system play important roles in neurologic diseases. However, little is known about the specific molecular pathways involved, and methods for their systematic identification are limited. Here, we developed a forward genetic screening platform that combines CRISPR-Cas9 perturbations, cell coculture in picoliter droplets, and microfluidic-based fluorescence-activated droplet sorting to identify mechanisms of cell-cell communication. We used SPEAC-seq (systematic perturbation of encapsulated associated cells followed by sequencing), in combination with in vivo genetic perturbations, to identify microglia-produced amphiregulin as a suppressor of disease-promoting astrocyte responses in multiple sclerosis preclinical models and clinical samples. Thus, SPEAC-seq enables the high-throughput systematic identification of cell-cell communication mechanisms.


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