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In vivo visualization and molecular targeting of the cardiac conduction system
William R. Goodyer, … , Eben L. Rosenthal, Sean M. Wu
William R. Goodyer, … , Eben L. Rosenthal, Sean M. Wu
Published August 11, 2022
Citation Information: J Clin Invest. 2022;132(20):e156955. https://doi.org/10.1172/JCI156955.
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Research Article Cardiology

In vivo visualization and molecular targeting of the cardiac conduction system

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Abstract

Accidental injury to the cardiac conduction system (CCS), a network of specialized cells embedded within the heart and indistinguishable from the surrounding heart muscle tissue, is a major complication in cardiac surgeries. Here, we addressed this unmet need by engineering targeted antibody-dye conjugates directed against the CCS, allowing for the visualization of the CCS in vivo following a single intravenous injection in mice. These optical imaging tools showed high sensitivity, specificity, and resolution, with no adverse effects on CCS function. Further, with the goal of creating a viable prototype for human use, we generated a fully human monoclonal Fab that similarly targets the CCS with high specificity. We demonstrate that, when conjugated to an alternative cargo, this Fab can also be used to modulate CCS biology in vivo, providing a proof of principle for targeted cardiac therapeutics. Finally, in performing differential gene expression analyses of the entire murine CCS at single-cell resolution, we uncovered and validated a suite of additional cell surface markers that can be used to molecularly target the distinct subcomponents of the CCS, each prone to distinct life-threatening arrhythmias. These findings lay the foundation for translational approaches targeting the CCS for visualization and therapy in cardiothoracic surgery, cardiac imaging, and arrhythmia management.

Authors

William R. Goodyer, Benjamin M. Beyersdorf, Lauren Duan, Nynke S. van den Berg, Sruthi Mantri, Francisco X. Galdos, Nazan Puluca, Jan W. Buikema, Soah Lee, Darren Salmi, Elise R. Robinson, Stephan Rogalla, Dillon P. Cogan, Chaitan Khosla, Eben L. Rosenthal, Sean M. Wu

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Figure 2

Optical clearing and 3D volumetric analyses on an intact heart following mCntn2-800 systemic injection reveals high-resolution labeling of the entire CCS.

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Optical clearing and 3D volumetric analyses on an intact heart following...
(A) Schematic representation of workflow for iDISCO+ clearing of mouse hearts and visualization using light-sheet microscopy. (B) iDISCO+ cleared heart harvested from a wild-type (CD1) mouse injected 2 days prior with mCntn2-800 (75 μg). Representative heart (n = 3) shown from 3 different angles of view: anterior-posterior (AP), right lateral (RL), and posterior-anterior (PA). Top and bottom rows are the same optically cleared heart using iDISCO+ where, in the top row, background fluorescence has been saturated to provide a representation of the opacified heart. Bottom row demonstrates the same tissue-cleared heart, showing near-infrared (800 nm) signal from mCntn2-800 marking the entire CCS. Conduction system components are labeled as indicated. Scale bar: 2 mm. AVN, atrioventricular node; His, His bundle; INT, internodal tracks; LA/RA, left or right atrium; LAVRB, left AV ring bundle; LBB/RBB, left or right bundle branch; LV/RV, left or right ventricle; PF, Purkinje fibers; RAVRB, right AV ring bundle; SAN, sinoatrial node.

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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