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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 Article has an altmetric score of 94

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 6

Nptn is enriched throughout the murine and human CCS.

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Nptn is enriched throughout the murine and human CCS.
Immunofluorescence...
Immunofluorescence staining of wild-type, postnatal day 10 mouse (A–D) (n = 3) and 65-year-old human (E–H) (n = 3) cardiac tissue sections. (A–D) Mouse CCS: anti-Nptn protein staining (cyan) within the (A) sinoatrial node (SAN) marked by Hcn4 (red); (B) atrioventricular node (AVN) labeled by Cpne5 (red); (C) His bundle (His), right bundle branch (RBB) and left bundle branch (LBB) indicated by Cpne5 (red); and (D) Purkinje fibers marked by Cx40 (red). DAPI (blue) in all panels. (E–H) Human CCS: Anti-NPTN (cyan) labeling the SAN, costained for HCN4 (red). Magnified region in SAN (F and H) indicated by white box in E. DAPI (blue). INT, internodal tracts; IVS, interventricular septum; LV, left ventricle; RA, right atrial myocardium. Scale bars: 100 μm (A, right images in C, and F), 200 μm (B), 50 μm (left image in C and D), and 400 μm (E).

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

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