Visualization of the Spiral Ganglion Neuron in Vivo Using a Novel <sup>177</sup> Lu Nuclear Molecule Label

For patients with severe and profound hearing loss, cochlear implant (CI), a common and effective modality for restoring hearing, directly stimulates spiral ganglion neurons (SGNs) to generate electrical activity and form auditory perception. However, the postoperative outcome of CI is significantly influenced by the number of surviving SGNs, ​​which is a key focus of preoperative evaluation​​. Existing audiologic function and radiographic tests cannot directly demonstrate the integrity of inner ear primary neurons. In this study, ​​we developed and validated​​ a radionuclide-labeled anti-vesicular glutamate transporter 1 (anti-VGLUT1) antibody-drug and achieved animal-level in vivo imaging of cochlear SGNs using nuclear imaging. By screening the public single-cell sequencing database, it is found that VGLUT1 can serve as a representative cell membrane marker for SGN in the cochlea. The potential of anti-VGLUT1 conjugated to the long half-life <sup>177</sup>Lu as a molecular probe to detect the relative number of SGNs in SGN-injured mouse and pig models is explored. The study provides a novel method for assessing cochlear nerve integrity in vivo by visualizing target antigen expression levels through nuclear imaging. This approach is promising to help CI candidates with preoperative inner ear SGN integrity assessment, contributing to clinical decision-making.

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Publication Details

Journal
Advanced Science
Published
2025-05-19
DOI
https://doi.org/10.1002/advs.202504464
Citations
1
Primary Topic
Axon Guidance and Neuronal Signaling
Type
article
Field-Weighted Citation Impact
0.91

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article

Visualization of the Spiral Ganglion Neuron in Vivo Using a Novel 177 Lu Nuclear Molecule Label

Kai Xu, Dawei Jiang, Yu Sun, Wen Li et al.
1 citations
Advanced Science
Axon Guidance and Neuronal Signaling
0.91
article

Visualization of the Spiral Ganglion Neuron in Vivo Using a Novel 177 Lu Nuclear Molecule Label

Kai Xu, Dawei Jiang, Yu Sun, Wen Li, Weiwei He, Chengwen Zheng, Xiaoli Lan, Xiaohui Wang, Hao Wang, Ge Yin, Jintao Yu, Chenyang Kong
article en
1 citations

Abstract

For patients with severe and profound hearing loss, cochlear implant (CI), a common and effective modality for restoring hearing, directly stimulates spiral ganglion neurons (SGNs) to generate electrical activity and form auditory perception. However, the postoperative outcome of CI is significantly influenced by the number of surviving SGNs, ​​which is a key focus of preoperative evaluation​​. Existing audiologic function and radiographic tests cannot directly demonstrate the integrity of inner ear primary neurons. In this study, ​​we developed and validated​​ a radionuclide-labeled anti-vesicular glutamate transporter 1 (anti-VGLUT1) antibody-drug and achieved animal-level in vivo imaging of cochlear SGNs using nuclear imaging. By screening the public single-cell sequencing database, it is found that VGLUT1 can serve as a representative cell membrane marker for SGN in the cochlea. The potential of anti-VGLUT1 conjugated to the long half-life <sup>177</sup>Lu as a molecular probe to detect the relative number of SGNs in SGN-injured mouse and pig models is explored. The study provides a novel method for assessing cochlear nerve integrity in vivo by visualizing target antigen expression levels through nuclear imaging. This approach is promising to help CI candidates with preoperative inner ear SGN integrity assessment, contributing to clinical decision-making.

Advanced ScienceVol. 12(29)
Union Hospital (HK), Huazhong University of Science and Technology (CN)
Emory University, National Natural Science Foundation of China, Chinese Academy of Sciences, Foundation for Innovative Research Groups of Hubei Province of China, Directorate for Biological Sciences, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities
Peace, Justice and strong institutions
Openalex Percentile: Top 27%
Axon Guidance and Neuronal Signaling
0.91
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