Author
Listed:
- Anthony T. Lee
(University of California, San Francisco
University of California, San Francisco)
- Edward F. Chang
(University of California, San Francisco
University of California, San Francisco)
- Mercedes F. Paredes
(University of California, San Francisco)
- Tomasz J. Nowakowski
(University of California, San Francisco
University of California, San Francisco
University of California, San Francisco
University of California, San Francisco)
Abstract
Advances in large-scale single-unit human neurophysiology, single-cell RNA sequencing, spatial transcriptomics and long-term ex vivo tissue culture of surgically resected human brain tissue have provided an unprecedented opportunity to study human neuroscience. In this Perspective, we describe the development of these paradigms, including Neuropixels and recent brain-cell atlas efforts, and discuss how their convergence will further investigations into the cellular underpinnings of network-level activity in the human brain. Specifically, we introduce a workflow in which functionally mapped samples of human brain tissue resected during awake brain surgery can be cultured ex vivo for multi-modal cellular and functional profiling. We then explore how advances in human neuroscience will affect clinical practice, and conclude by discussing societal and ethical implications to consider. Potential findings from the field of human neuroscience will be vast, ranging from insights into human neurodiversity and evolution to providing cell-type-specific access to study and manipulate diseased circuits in pathology. This Perspective aims to provide a unifying framework for the field of human neuroscience as we welcome an exciting era for understanding the functional cytoarchitecture of the human brain.
Suggested Citation
Anthony T. Lee & Edward F. Chang & Mercedes F. Paredes & Tomasz J. Nowakowski, 2024.
"Large-scale neurophysiology and single-cell profiling in human neuroscience,"
Nature, Nature, vol. 630(8017), pages 587-595, June.
Handle:
RePEc:nat:nature:v:630:y:2024:i:8017:d:10.1038_s41586-024-07405-0
DOI: 10.1038/s41586-024-07405-0
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