Localization of unlabeled bepirovirsen antisense oligonucleotide in murine tissues using in situ hybridization and CARS imaging

被引:2
|
作者
Spencer-Dene, Bradley [1 ]
Mukherjee, Prabuddha [2 ,3 ]
Alex, Aneesh [2 ,4 ]
Bera, Kajari [2 ,3 ]
Tseng, Wei-Ju [4 ]
Shi, Jindou [2 ,5 ]
Chaney, Eric J. [2 ,3 ]
Spillman, Darold R. [2 ,3 ]
Marjanovic, Marina [2 ,3 ,6 ,7 ]
Miranda, Elena [1 ]
Boppart, Stephen A. [2 ,3 ,5 ,6 ,7 ]
Hood, Steve R. [1 ,2 ]
机构
[1] GSK, Vitro Vivo Translat, BioImaging, Stevenage SG1 2NY, England
[2] Univ Illinois Urbana & Champaign, Ctr Biophys & Computat Biol, Urbana, IL 61801 USA
[3] Univ Illinois Urbana & Champaign, Beckman Inst Adv Sci & Technol, Urbana, IL 61801 USA
[4] GSK, Vitro Vivo Translat, BioImaging, Upper Providence, PA 19426 USA
[5] Univ Illinois, Dept Elect & Comp Engn, Urbana, IL 61801 USA
[6] Univ Illinois, Dept Bioengn, Urbana, IL 61801 USA
[7] Univ Illinois, Carle Illinois Coll Med, Urbana, IL 61801 USA
关键词
label-free imaging; antisense oligonucleotides; in situ hybridization; miRNAscope; multiphoton imaging; coherent anti-Stokes Raman scattering; pharmacokinetics; RAMAN-SCATTERING MICROSCOPY; PHOSPHOROTHIOATE OLIGODEOXYNUCLEOTIDES; HEPATITIS-B; PHARMACOKINETICS; RNA; SPECTROSCOPY; CHALLENGES; REDUCTION; KNOCKOUT; DELIVERY;
D O I
10.1261/rna.079699.123
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Current methods for detecting unlabeled antisense oligonucleotide (ASO) drugs rely on immunohistochemistry (IHC) and/or conjugated molecules, which lack sufficient sensitivity, specificity, and resolution to fully investigate their biodistribution. Our aim was to demonstrate the qualitative and quantitative distribution of unlabeled bepirovirsen, a clinical stage ASO, in livers and kidneys of dosed mice using novel staining and imaging technologies at subcellular resolution. ASOs were detected in formalin-fixed paraffin-embedded (FFPE) and frozen tissues using an automated chromogenic in situ hybridization (ISH) assay: miRNAscope. This was then combined with immunohistochemical detection of cell lineage markers. ASO distribution in hepatocytes versus nonparenchymal cell lineages was quantified using HALO AI image analysis. To complement this, hyperspectral coherent anti-Stokes Raman scattering (HS-CARS) imaging microscopy was used to specifically detect the unique cellular Raman spectral signatures following ASO treatment. Bepirovirsen was localized primarily in nonparenchymal liver cells and proximal renal tubules. Codetection of ASO with distinct cell lineage markers of liver and kidney populations aided target cell identity facilitating quantification. Positive liver signal was quantified using HALO AI, with 12.9% of the ASO localized to the hepatocytes and 87.1% in nonparenchymal cells. HS-CARS imaging specifically detected ASO fingerprints based on the unique vibrational signatures following unlabeled ASO treatment in a totally nonperturbative manner at subcellular resolution. Together, these novel detection and imaging modalities represent a significant increase in our ability to detect unlabeled ASOs in tissues, demonstrating improved levels of specificity and resolution. These methods help us understand their underlying mechanisms of action and ultimately improve the therapeutic potential of these important drugs for treating globally significant human diseases.
引用
收藏
页码:1575 / 1590
页数:16
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