Primary Cell Culture of Live Neurosurgically Resected Aged Adult Human Brain Cells and Single Cell Transcriptomics

Jennifer Spaethling(University of Pennsylvania), Young-Ji Na(University of Pennsylvania), Jaehee Lee(University of Pennsylvania), Alexandra V. Ulyanova(University of Pennsylvania), Gordon H. Baltuch(University of Pennsylvania), Thomas J. Bell(University of Pennsylvania), Steven Brem(University of Pennsylvania), H. Isaac Chen(University of Pennsylvania), Hannah Dueck(University of Pennsylvania), Stephen Fisher(University of Pennsylvania), Marcela P. Garcia(University of Pennsylvania), Mugdha Khaladkar(University of Pennsylvania), David Kung(University of Pennsylvania), Timothy H. Lucas(University of Pennsylvania), Donald M. O’Rourke(University of Pennsylvania), Derek Stefanik(University of Pennsylvania), Jinhui Wang(University of Pennsylvania), John A. Wolf(University of Pennsylvania), Tamás Bartfai(Stockholm University), M. Sean Grady(University of Pennsylvania), Jai‐Yoon Sul(University of Pennsylvania), Junhyong Kim(University of Pennsylvania), James Eberwine(University of Pennsylvania)
Cell Reports
January 1, 2017
Cited by 73Open Access
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Abstract

Investigation of human CNS disease and drug effects has been hampered by the lack of a system that enables single-cell analysis of live adult patient brain cells. We developed a culturing system, based on a papain-aided procedure, for resected adult human brain tissue removed during neurosurgery. We performed single-cell transcriptomics on over 300 cells, permitting identification of oligodendrocytes, microglia, neurons, endothelial cells, and astrocytes after 3 weeks in culture. Using deep sequencing, we detected over 12,000 expressed genes, including hundreds of cell-type-enriched mRNAs, lncRNAs and pri-miRNAs. We describe cell-type- and patient-specific transcriptional hierarchies. Single-cell transcriptomics on cultured live adult patient derived cells is a prime example of the promise of personalized precision medicine. Because these cells derive from subjects ranging in age into their sixties, this system permits human aging studies previously possible only in rodent systems.


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