Neural plasticity explored by correlative two-photon and electron/spim microscopy

Anno: 2013

Autori: Mascaro A.L.Allegra, Silvestri L., Costantini I., Sacconi L., Maco B., Knott G.W., Pavone F.S.

Affiliazione autori: LENS, University of Florence, Sesto Fiorentino, Italy; Ctr. Interdisciplinaire de Microscopie Electronique, Ecole Polytechnique Federale de Lausanne, Lausanne, Switzerland

Abstract: Plasticity of the central nervous system is a complex process which involves the remodeling of neuronal processes and synaptic contacts. However, a single imaging technique can reveal only a small part of this complex machinery. To obtain a more complete view, complementary approaches should be combined. Two-photon fluorescence microscopy, combined with multi-photon laser nanosurgery, allow following the real-time dynamics of single neuronal processes in the cerebral cortex of living mice. The structural rearrangement elicited by this highly confined paradigm of injury can be imaged in vivo first, and then the same neuron could be retrieved ex-vivo and characterized in terms of ultrastructural features of the damaged neuronal branch by means of electron microscopy. Afterwards, we describe a method to integrate data from in vivo two-photon fluorescence imaging and ex vivo light sheet microscopy, based on the use of major blood vessels as reference chart. We show how the apical dendritic arbor of a single cortical pyramidal neuron imaged in living mice can be found in the large-scale brain reconstruction obtained with light sheet microscopy. Starting from its apical portion, the whole pyramidal neuron can then be segmented and located in the correct cortical layer. With the correlative approach presented here, researchers will be able to place in a three-dimensional anatomic context the neurons whose dynamics have been observed with high detail in vivo.

Titolo Convegno:

Parole chiavi: Blood vessels; Brain; Imaging techniques; Light; Mammals; Multiphoton processes; Photons; Three dimensional, 3D reconstruction; Axotomy; In-Vivo imaging; Light-sheet microscopies; Neuronal regrowth, Neurons
DOI: 10.1117/12.2032505