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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 5

scRNA-seq analyses reveal cell surface markers within distinct components of the CCS for generating targeted optical imaging tools.

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scRNA-seq analyses reveal cell surface markers within distinct component...
(A) Workflow of single-cell RNA sequencing (scRNAseq) analyses to uncover cell-surface-protein genes enriched within the murine CCS subcomponents, including the sinoatrial node (SAN), atrioventricular node (AVN), His bundle (His), and Purkinje fiber (PF) cells, as compared with all other cardiac cell types. (B) Immunofluorescence (IF) staining of wild-type murine, embryonic day 16.5 cardiac tissue sections (n = 3 per marker). Distinct CCS components shown, including the SAN, AVN, His, bundle branches (BB), and PF cells (each component outlined by a solid line) for 2 validated gene markers, Gfra2 and Epha4. DAPI (blue) in all images. Top panel: IF with staining against Gfra2 protein (cyan) and known markers Hcn4 (SAN, red), Cx40 (His, BB and PF, green), and Pgp9.5 (neurons, green or red as indicated). Transitional cells demarcated by hashed lines. Bottom panel: IF with staining against Epha4 protein (cyan) and known markers Hcn4 (SAN, red), Cpne5 (AVN, red), and Cx40 (His, BB and PF, green). cSAN, compact SAN; INT, internodal tract; IVS, interventricular septum; MV, mitral valve; LA, left atrial myocardium; LBB, left bundle branch; LV, left ventricle; PMJ, Purkinje-myocyte junction; Prox, proximal; RA, right atrial myocardium; RBB, right bundle branch; SAN Tz, SA nodal transitional cells; VM, ventricular myocardium. Scale bars: 100 μm (SAN, AVN [top]), 200 μm (AVN [bottom]), and 50 μm (His, PF).

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

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