Multicolor multiscale brain imaging with chromatic multiphoton serial microscopy

Autor: Karine Loulier, Ignacio Arganda-Carreras, Xavier Solinas, Stephen G. Turney, Jean Livet, Solène Clavreul, Willy Supatto, Pierre Mahou, Alexis-Pierre Bemelmans, Emmanuel Beaurepaire, Jeff W. Lichtman, Katherine Matho, Anatole Chessel, Lamiae Abdeladim, Jean-Marc Sintes
Přispěvatelé: Laboratoire d'Optique et Biosciences (LOB), École polytechnique (X)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Institut de la Vision, Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Cold Spring Harbor Laboratory (CSHL), University of the Basque Country/Euskal Herriko Unibertsitatea (UPV/EHU), Donostia International Physics Center - DIPC (SPAIN), Donostia International Physics Center (DIPC), University of the Basque Country/Euskal Herriko Unibertsitatea (UPV/EHU)-University of the Basque Country/Euskal Herriko Unibertsitatea (UPV/EHU), Department of Molecular and Cellular Biology, and Center for Brain Science, Harvard University, Institut de Biologie François JACOB (JACOB), Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Harvard University [Cambridge], Arnoux, Aurélien, Centre National de la Recherche Scientifique (CNRS)-Sorbonne Université (SU)-Institut National de la Santé et de la Recherche Médicale (INSERM)
Rok vydání: 2019
Předmět:
0301 basic medicine
General Physics and Astronomy
02 engineering and technology
Nestin
Mice
Parvovirinae
generation
Microscopy
Multiphoton excitation
double markers
lcsh:Science
Cerebral Cortex
[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]
Multidisciplinary
Pyramidal Cells
Resolution (electron density)
Dependovirus
organization
021001 nanoscience & nanotechnology
Fluorescence
Neuroanatomical Tract-Tracing Techniques
[SDV.MHEP.OS] Life Sciences [q-bio]/Human health and pathology/Sensory Organs
Models
Animal

Female
0210 nano-technology
[PHYS.PHYS.PHYS-OPTICS] Physics [physics]/Physics [physics]/Optics [physics.optics]
Materials science
ex-vivo
Channel (digital image)
fluorescent proteins
Science
Genetic Vectors
Color
Mice
Transgenic

Neuroimaging
Transfection
General Biochemistry
Genetics and Molecular Biology

03 medical and health sciences
Imaging
Three-Dimensional

Optics
Animals
Humans
Image acquisition
Chromatic scale
[SDV.MHEP.OS]Life Sciences [q-bio]/Human health and pathology/Sensory Organs
gene
axonal projections
business.industry
General Chemistry
cell
mosaic analysis
Mice
Inbred C57BL

Luminescent Proteins
HEK293 Cells
Microscopy
Fluorescence
Multiphoton

030104 developmental biology
mouse-brain
Astrocytes
lcsh:Q
business
Zdroj: Nature Communications
Nature Communications, 2019, 10 (1), pp.1662. ⟨10.1038/s41467-019-09552-9⟩
Nature Communications, Vol 10, Iss 1, Pp 1-14 (2019)
Nature Communications, Nature Publishing Group, 2019, 10 (1), pp.1662. ⟨10.1038/s41467-019-09552-9⟩
Addi. Archivo Digital para la Docencia y la Investigación
instname
ISSN: 2041-1723
DOI: 10.1038/s41467-019-09552-9
Popis: Large-scale microscopy approaches are transforming brain imaging, but currently lack efficient multicolor contrast modalities. We introduce chromatic multiphoton serial (ChroMS) microscopy, a method integrating one-shot multicolor multiphoton excitation through wavelength mixing and serial block-face image acquisition. This approach provides organ-scale micrometric imaging of spectrally distinct fluorescent proteins and label-free nonlinear signals with constant micrometer-scale resolution and sub-micron channel registration over the entire imaged volume. We demonstrate tridimensional (3D) multicolor imaging over several cubic millimeters as well as brain-wide serial 2D multichannel imaging. We illustrate the strengths of this method through color-based 3D analysis of astrocyte morphology and contacts in the mouse cerebral cortex, tracing of individual pyramidal neurons within densely Brainbow-labeled tissue, and multiplexed whole-brain mapping of axonal projections labeled with spectrally distinct tracers. ChroMS will be an asset for multiscale and system-level studies in neuroscience and beyond. We thank Minh-Son Phan, Samuel Tozer, and Z. Josh Huang for scientific discussions and comments on the manuscript. We thank TissueVision for providing technical advice for the implementation and customization of the block-face system. We thank Bastien Binet from Polytechnique Polymedia center for his generous help in the creation of 3D graphics. We thank IdV core imaging, animal experimentation and histology facilities for technical assistance. This work was supported by fellowships from Universite Paris-Saclay (Initiatives Doctorales Interdisciplinaires) to L.A., Ecole des Neurosciences de Paris to K.M., Region Ile-de-France and Fondation ARC pour la Recherche sur le Cancer to S.C. by Agence Nationale de la Recherche under contracts ANR-11-EQPX-0029 (Equipex Morphoscope2), ANR-10-INBS-04 (France BioImaging), and ANR-10-LABX-65 (LabEx LifeSenses), by Fondation pour la Recherche Medicale (grant DBI20141231328), by Target ALS and by the European Research Council (ERC-CoG 649117).
Databáze: OpenAIRE