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組織透明化在神經科學領域中的應用

瀏覽次數(shù):1176 發(fā)布日期:2022-2-10  來源:锘海生命科學
當神經科學邂逅組織透明化——會演繹出怎樣的故事?

神經科學是一門神秘的科學,也一直是生命科學研究的熱點。如果有一天,我們可以搞明白神經細胞是怎么一回事,神經細胞之間是如何協(xié)作的,或許我們就能明白意識是如何產生的了?明白了我們?yōu)槭裁匆X?明白了男人和女人的大腦有什么不一樣?為了明確神經元的結構和功能連接,需要對整個大腦和脊髓中的神經元及突觸進行成像和追蹤。組織透明化技術的發(fā)展使生物樣本變得透明,為生物組織結構的三維可視化研究打開了大門,并為進一步探索人類疾病的復雜性提供了嶄新的平臺,近年來組織透明化技術在生物醫(yī)學研究領域得到了廣泛應用。

BRADKE等利用3DISCO透明化技術和光片顯微鏡成像技術識別、追蹤和評估脊髓損傷后的軸突再生,確定了軸突再生能力及再生軸突軌跡,有助于解釋軸突再生機制,同時定量測定了脊髓損傷后神經膠質的活動反應。

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.

總之,組織透明技術結合顯微成像技術,極大推動了全身或全器官成像的進程,有助于加強對完整生物系統(tǒng)的綜合理解,為神經科學研究提供了更加細致的信息,是神經科學研究領域強有利的工具。

目前組織透明化方法有油性,基于水凝膠和水性的組織透明化方法。其中油性組織透明化方法主要有BABB, 3DISCO, uDISCO,F(xiàn)DISCO和 PEGASOS等,基于水凝膠的透明化方法有CLARITY和SHIELD,水性組織透明化方法有CLearT/CLearT2,SeeDB, FRUIT, Scale和CUBIC等方法。而锘海研發(fā)的透明化試劑盒依托測樣服務中積累到的豐富而寶貴的經驗,對各種透明化方法進行測試和比較后對試劑配方進行了精心優(yōu)化,使其在組織熒光保護、樣本形態(tài)維持、降低自發(fā)熒光等方面表現(xiàn)出非常優(yōu)異的性能,是研究神經科學的不二之選。


                                                    锘海組織透明化試劑盒  

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.
2. Liebmann T, Renier N, Bettayeb K, Greengard P, Tessier-Lavigne M, Flajolet M. Three-Dimensional Study of Alzheimer's Disease Hallmarks Using the iDISCO Clearing Method. Cell Rep. 2016 Jul 26;16(4):1138-1152. doi: 10.1016/j.celrep.2016.06.060. Epub 2016 Jul 14. PMID: 27425620; PMCID: PMC5040352.
3. Chung K, Wallace J, Kim SY, Kalyanasundaram S, Andalman AS, Davidson TJ, Mirzabekov JJ, Zalocusky KA, Mattis J, Denisin AK, Pak S, Bernstein H, Ramakrishnan C, Grosenick L, Gradinaru V, Deisseroth K. Structural and molecular interrogation of intact biological systems. Nature. 2013 May 16;497(7449):332-7. doi: 10.1038/nature12107. Epub 2013 Apr 10. PMID: 23575631; PMCID: PMC4092167.
4. Murakami TC, Mano T, Saikawa S, Horiguchi SA, Shigeta D, Baba K, Sekiya H, Shimizu Y, Tanaka KF, Kiyonari H, Iino M, Mochizuki H, Tainaka K, Ueda HR. A three-dimensional single-cell-resolution whole-brain atlas using CUBIC-X expansion microscopy and tissue clearing. Nat Neurosci. 2018 Apr;21(4):625-637. doi: 10.1038/s41593-018-0109-1. Epub 2018 Mar 5. PMID: 29507408.
5. Tian T, Yang Z, Li X. Tissue clearing technique: Recent progress and biomedical applications. J Anat. 2021 Feb;238(2):489-507. doi: 10.1111/joa.13309. Epub 2020 Sep 16. PMID: 32939792; PMCID: PMC7812135.
 
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