4.6 Article

Rapid, label-free identification of cerebellar structures using multiphoton microscopy

Journal

JOURNAL OF BIOPHOTONICS
Volume 10, Issue 12, Pages 1617-1626

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/jbio.201600297

Keywords

cerebellar structures; multiphoton microscopy (MPM); image analysis; second harmonic generation (SHG); two-photon excited fluorescence (TPEF)

Funding

  1. National High Technology Research and Development Program of China [2015AA020508]
  2. National Natural Science Foundation of China [81671730]
  3. National Key Basic Research Program of China [2015CB352006]
  4. Joint Funds of Fujian Provincial Health and Education Research [WKJ2016-2-28]
  5. Program for Changjiang Scholars and Innovative Research Team in University [IRT_15R10]

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The cerebellum is the prominent laminar structure of the mammalian brain that has been implicated in various psychiatric and neurological diseases. Although clinical brain imaging techniques have provided precise anatomic images of cerebellar structures, a definitive diagnosis still requires adequate resolution to identify individual layers in cerebellar cortex, the extent of tumor, even requires the histological tissue examination during surgical procedures. In this study, multiphoton microscopy (MPM), based on second harmonic generation (SHG) and two-photon excited fluorescence (TPEF), was perform on the rat cerebellar structures and pathology with the combination of image analysis methods. Results show that MPM can reveal the cerebellar vermis, hemispheres, medulla, and ventricle, as well as axon bundles, Purkinje cells, capillaries, and the pia mater of the cerebellum. Together with custom-developed image processing algorithms, MPM could further differentiate between the gray and white matter, as well as evaluate the Purkinje cell layer, identify the cerebellar tumor boundary, and distinguish between the tumor core and peritumor regions. Our results establish a direct visualization and rapid assessment approach for the cerebellar structures, as well as suggest the feasibility of in vivo multiphoton microendoscopes and fiberscopes as clinical tools for neuropathological diagnoses. [GRAPHICS] .

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