Imaging large regions of the spinal cord of GFP-M mice
(a) Entire spinal cord of a GFP-M mouse cut into 3- to 4-mm-long segments, cleared and imaged with ultramicroscopy. (b) Drawing of the ultramicroscopy setup showing tissue positioning and the light path. (c) A spinal cord segment (length 4 mm, T12 to L2 spine level) of a GFP-M mouse scanned with ultramicroscopy shown in a horizontal view. (d) Cross-view projection (50-µm thickness) of the indicated region in c. White arrows in c,d mark individual axons in the white matter; red arrows mark cell bodies in the gray matter. (e) Traced white and gray matter boundaries and axon bundles (yellow arrows).
阿爾茲海默癥(AD)是一種起病隱匿的進行性發(fā)展的神經系統(tǒng)退行性疾病。臨床上以記憶障礙、失語、失用、失認、視空間技能損壞、執(zhí)行功能障礙以及人格和行為改變等全面性癡呆表現(xiàn)為特征,細胞外β淀粉樣蛋白沉積和細胞內tau蛋白磷酸化是AD的主要病理特征。Liebmann等人利用iDISCO技術對阿爾茲海默癥模型小鼠腦進行透明化闡明了β淀粉樣蛋白沉積和小膠質細胞及脈管系統(tǒng)之間的空間分布關系,這將對阿爾茲海默癥的科學研究和治療產生重大意義。
Double Labeling of β-Amyloid Plaques and Reactive Microgliosis, Axonal Dystrophy, or Vasculature in Cleared AD Brains with Volume Imaging
(A)confocal image of β-amyloid plaques and cell nuclei double staining in a 17-month-old2xTg AD cleared mouse brain. (B) Confocal optical slices of microglia stained with anti-Iba1 antibody. (C) 3D surface rendering of four isolated β-amyloid plaques and neighboring microglia cells from the AD brain described in (B). (D)Maximum intensity projection of β-amyloid plaques and neuro filament H staining in a10-month-old 2xTgAD cleared mouse cortex(500mmthick). (E)Magnified region from (D) showing labeled axons in absence of β-amyloid plaques. (F) Magnified region from (D) showing dystrophic axons surrounding labeled β-amyloid plaques. (G) Maximum intensity projection of optical section (1mm) from the cortex of an 11-month-old 2xTgAD mouse brain labeled for plaques (anti-b amyloid anti-bodies) and vasculature. (H)Maximum intensity projection of optical section (1mm) from the cortex and hippocampus of an 8-month-old 2xTgAD mouse brain labeled for plaques (Congored) and vasculature.
Chung等人通過CLARITY技術獲得透明而完整的小鼠大腦,利用Thy1–eYFP信號實現(xiàn)了對小鼠大腦神經元進行遠距離投射、神經回路、細胞關系、亞細胞結構、蛋白質復合物、 核酸和神經遞質的成像。展現(xiàn)了大腦中復雜的精細連接和分子結構。
Intact adult mouse brain imaging
a, Cajal quote before CLARITY. b, Cajal quote after CLARITY: Thy1–eYFP line-H mouse brain after hydrogel–tissue hybridization, ETC and refractive-index matching. c, Fluorescence image of brain depicted in b. d, Dorsal aspect is imaged, then brain is inverted and ventral aspect imaged. e, Three-dimensional rendering of clarified brain imaged;f, Non sectioned mouse brain tissue showing cortex, hippocampus and thalamus;g–l, Optical sections from f showing negligible resolution;m, Cross-section of axons in clarified Thy1–channelrhodopsin2 (ChR2)–eYFP striatum;n, Dendrites and spines of neurons in clarified Thy1–eYFP line-H cortex.
MURAKAMI等人應用CUBIC-X透明并膨大小鼠大腦,在亞細胞水平對整個小鼠大腦進行成像,并繪制出了一張小鼠大腦圖譜。他們采用化學方法標記了大腦中的每個細胞,然后在大腦透明化的同時將其尺寸擴大了十倍,利用精密成像技術對神經元進行了三維重建,總計約7200萬個細胞。
Construction of a single-cell-resolution mouse brain atlas (CUBIC-Atlas)
a, Overview of construction of the CUBIC-Atlas. b, The CUBIC-Atlas. Horizontal, sagittal and coronal view of single-plane images (left) and volume-rendered images (right) of the CUBIC-Atlas. c–j, Major anatomical areas in the CUBIC-Atlas. k, Overview of whole-brain cell counting in C57BL/6N 8-week-old male mice. l, Cell numbers in each brain area.
參考文獻:
1. Ertürk A, Mauch CP, Hellal F, Förstner F, Keck T, Becker K, Jährling N, Steffens H, Richter M, Hübener M, Kramer E, Kirchhoff F, Dodt HU, Bradke F. Three-dimensional imaging of the unsectioned adult spinal cord to assess axon regeneration and glial responses after injury. Nat Med. 2011 Dec 25;18(1):166-71. doi: 10.1038/nm.2600. PMID: 22198277.