Tailored Sample Mounting for Light-Sheet Fluorescence Microscopy of Clarified Specimens by Polydimethylsiloxane Casting

被引:8
|
作者
Di Giovanna, Antonino Paolo [1 ]
Credi, Caterina [1 ,2 ]
Franceschini, Alessandra [1 ]
Mullenbroich, Marie Caroline [3 ]
Silvestri, Ludovico [1 ,4 ]
Pavone, Francesco Saverio [1 ,4 ,5 ]
机构
[1] Univ Florence, European Lab Nonlinear Spect, Sesto Fiorentino, Italy
[2] Univ Florence, Dept Informat Engn DINFO, Florence, Italy
[3] Univ Glasgow, Sch Phys & Astron, Glasgow, Lanark, Scotland
[4] CNR, Natl Inst Opt, Florence, Italy
[5] Univ Florence, Dept Phys & Astron, Sesto Fiorentino, Italy
来源
FRONTIERS IN NEUROANATOMY | 2019年 / 13卷
基金
欧盟地平线“2020”;
关键词
light-sheet microscopy; tissue clearing; brain; sample mounting; PDMS;
D O I
10.3389/fnana.2019.00035
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
The combination of biological tissue clearing methods with light-sheet fluorescence microscopy (LSFM) allows acquiring images of specific biological structures of interest at whole organ scale and microscopic resolution. Differently to classical epifluorescence techniques, where the sample is cut into slices, LSFM preserves the whole organ architecture, which is of particular relevance for investigations of long-range neuronal circuits. This imaging modality comes with the need of new protocols for sample mounting. Gel matrix, hooks, tips, glues, and quartz cuvettes have been used to keep whole rodent organs in place during image acquisitions. The last one has the advantage of avoiding sample damage and optical aberrations when using a quartz refractive index (RI) matching solution. However, commercially available quartz cuvettes for such large samples are expensive. We propose the use of polydimethylsiloxane (PDMS) for creating tailor-made cuvettes for sample holding. For validation, we compared PDMS and quartz cuvettes by measuring light transmittance and performing whole mouse-brain imaging with LSFM. Moreover, imaging can be performed using an inexpensive RI matching solution, which further reduces the cost of the imaging process. Worth of note, the RI matching solution used in combination with PDMS leads to a moderate expansion of the sample with respect to its original size, which may represent an advantage when investigating small components, such as neuronal processes. Overall, we found the use of custom-made PDMS cuvettes advantageous in term of cost, image quality, or preservation of sample integrity with respect to other whole-mouse brain mounting strategies adopted for LSFM.
引用
收藏
页数:10
相关论文
共 50 条
  • [1] Light-sheet based fluorescence microscopy: the dark side of the sample finally revealed
    Girard, Philippe P.
    Forget, Benoit C.
    M S-MEDECINE SCIENCES, 2011, 27 (8-9): : 753 - 762
  • [2] Light-sheet light-field fluorescence microscopy
    Liang, Dong
    Peng, Xiaoting
    Hu, Yuyao
    Zhao, Fu
    Zheng, Shanshan
    Situ, Guohai
    Liu, Jun
    OPTICS AND LASERS IN ENGINEERING, 2022, 153
  • [3] Progress in Light-Sheet Fluorescence Microscopy and Applications
    Yu Xianghua
    Liu Chao
    Bai Chen
    Yang Yanlong
    Peng Tong
    Dan Dan
    Min Junwei
    Yao Baoli
    LASER & OPTOELECTRONICS PROGRESS, 2020, 57 (10)
  • [4] Light-sheet fluorescence microscopy for quantitative biology
    Stelzer, Ernst H. K.
    NATURE METHODS, 2015, 12 (01) : 23 - 26
  • [5] Light-sheet fluorescence microscopy for quantitative biology
    Ernst H K Stelzer
    Nature Methods, 2015, 12 : 23 - 26
  • [6] Doubling the resolution of light-sheet fluorescence microscopy
    Fiolka, Reto
    NATURE METHODS, 2022, 19 (11) : 1355 - 1356
  • [7] Doubling the resolution of light-sheet fluorescence microscopy
    Nature Methods, 2022, 19 : 1355 - 1356
  • [8] Imaging the Aging Cochlea with Light-Sheet Fluorescence Microscopy
    Santi, Peter A.
    Johnson, Shane B.
    JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2022, (187):
  • [9] A guide to light-sheet fluorescence microscopy for multiscale imaging
    Rory M Power
    Jan Huisken
    Nature Methods, 2017, 14 : 360 - 373
  • [10] Light-sheet Fluorescence Microscopy for the Study of the Murine Heart
    Ding, Yichen
    Bailey, Zachary
    Messerschmidt, Victoria
    Nie, Jun
    Bryant, Richard
    Rugonyi, Sandra
    Fei, Peng
    Lee, Juhyun
    Hsiai, Tzung K.
    JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2018, (139):