Structural and molecular interrogation of intact biological systems
被引:1544
作者:
Chung, Kwanghun
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机构:
Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
Stanford Univ, CNC Program, Stanford, CA 94305 USAStanford Univ, Dept Bioengn, Stanford, CA 94305 USA
Chung, Kwanghun
[1
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Wallace, Jenelle
[1
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Kim, Sung-Yon
[1
]
Kalyanasundaram, Sandhiya
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机构:
Stanford Univ, CNC Program, Stanford, CA 94305 USAStanford Univ, Dept Bioengn, Stanford, CA 94305 USA
Kalyanasundaram, Sandhiya
[2
]
Andalman, Aaron S.
论文数: 0引用数: 0
h-index: 0
机构:
Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
Stanford Univ, CNC Program, Stanford, CA 94305 USAStanford Univ, Dept Bioengn, Stanford, CA 94305 USA
Andalman, Aaron S.
[1
,2
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Davidson, Thomas J.
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机构:
Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
Stanford Univ, CNC Program, Stanford, CA 94305 USAStanford Univ, Dept Bioengn, Stanford, CA 94305 USA
Davidson, Thomas J.
[1
,2
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Mirzabekov, Julie J.
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机构:
Stanford Univ, Dept Bioengn, Stanford, CA 94305 USAStanford Univ, Dept Bioengn, Stanford, CA 94305 USA
Mirzabekov, Julie J.
[1
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Zalocusky, Kelly A.
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机构:
Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
Stanford Univ, CNC Program, Stanford, CA 94305 USAStanford Univ, Dept Bioengn, Stanford, CA 94305 USA
Zalocusky, Kelly A.
[1
,2
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Mattis, Joanna
[1
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Denisin, Aleksandra K.
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Stanford Univ, Dept Bioengn, Stanford, CA 94305 USAStanford Univ, Dept Bioengn, Stanford, CA 94305 USA
Denisin, Aleksandra K.
[1
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Pak, Sally
[1
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Bernstein, Hannah
[1
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Ramakrishnan, Charu
[1
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Grosenick, Logan
[1
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Gradinaru, Viviana
论文数: 0引用数: 0
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机构:
Stanford Univ, CNC Program, Stanford, CA 94305 USAStanford Univ, Dept Bioengn, Stanford, CA 94305 USA
Gradinaru, Viviana
[2
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Deisseroth, Karl
[1
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机构:
[1] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[2] Stanford Univ, CNC Program, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Psychiat & Behav Sci, Stanford, CA 94305 USA
[4] Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA
Obtaining high-resolution information from a complex system, while maintaining the global perspective needed to understand system function, represents a key challenge in biology. Here we address this challenge with a method (termed CLARITY) for the transformation of intact tissue into a nanoporous hydrogel-hybridized form (crosslinked to a three-dimensional network of hydrophilic polymers) that is fully assembled but optically transparent and macromolecule-permeable. Using mouse brains, we show intact-tissue imaging of long-range projections, local circuit wiring, cellular relationships, subcellular structures, protein complexes, nucleic acids and neurotransmitters. CLARITY also enables intact-tissue in situ hybridization, immunohistochemistry with multiple rounds of staining and de-staining in non-sectioned tissue, and antibody labelling throughout the intact adult mouse brain. Finally, we show that CLARITY enables fine structural analysis of clinical samples, including non-sectioned human tissue from a neuropsychiatric-disease setting, establishing a path for the transmutation of human tissue into a stable, intact and accessible form suitable for probing structural and molecular underpinnings of physiological function and disease.