共 6 条
Structural neurobiology: missing link to a mechanistic understanding of neural computation
被引:143
作者:
Denk, Winfried
[1
]
Briggman, Kevin L.
[2
]
Helmstaedter, Moritz
[3
]
机构:
[1] Max Planck Inst Med Res, D-69120 Heidelberg, Germany
[2] NINDS, Bethesda, MD 20892 USA
[3] Max Planck Inst Neurobiol, D-82152 Martinsried, Germany
关键词:
WHOLE-CELL RECORDINGS;
NETWORK ACTIVITY;
SINGLE;
TISSUE;
FLUORESCENCE;
EXPRESSION;
MICROSCOPY;
SYNAPSES;
CONTRAST;
NEURONS;
D O I:
10.1038/nrn3169
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
High-resolution, comprehensive structural information is often the final arbiter between competing mechanistic models of biological processes, and can serve as inspiration for new hypotheses. In molecular biology, definitive structural data at atomic resolution are available for many macromolecules; however, information about the structure of the brain is much less complete, both in scope and resolution. Several technical developments over the past decade, such as serial block-face electron microscopy and trans-synaptic viral tracing, have made the structural biology of neural circuits conceivable: we may be able to obtain the structural information needed to reconstruct the network of cellular connections for large parts of, or even an entire, mouse brain within a decade or so. Given that the brain's algorithms are ultimately encoded by this network, knowing where all of these connections are should, at the very least, provide the data needed to distinguish between models of neural computation.
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页码:351 / 358
页数:8
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