# An ultrasound-scanning in vivo light source

**Authors:** Shan Jiang, Marigold G. Malinao, Fan Yang, Yushun Zeng, Silky S. Hou, Xiang Wu, Nicholas J. Rommelfanger, Lata Chaunsali, Jun Ding, Xiaoke Chen, Qifa Zhou, Harald Sontheimer, Guosong Hong

PMC · DOI: 10.21203/rs.3.rs-6773130/v1 · 2025-06-19

## TL;DR

This paper introduces a non-invasive method using ultrasound to generate light deep inside the body for precise biological control.

## Contribution

A novel in vivo light source using ultrasound-scanning mechanoluminescent nanotransducers for dynamic deep-tissue optical interfacing.

## Key findings

- The approach enables programmable light patterning in tissue-mimicking phantoms and animal circulatory systems.
- The system allows dynamic 3D brain targeting and behavioral control in freely moving animals.
- Functionality was validated through electrophysiological recordings and immunostaining in opsin-expressing neurons.

## Abstract

Biological systems operate across distributed regions with fast, localized dynamics, yet existing biointerfaces fail short in providing both high spatiotemporal precision and the ability to dynamically target any region without disturbing surrounding tissue. Here, we present an in vivo deep-tissue light source based on focused ultrasound (FUS) scanning of mechanoluminescent nanotransducers (MLNTs) circulating through the vasculature. We demonstrate the programmability of this approach in tissue-mimicking phantoms and the endogenous circulatory system of animals, where tunable spatial resolution and dynamic light patterning can be achieved. We validate the functionality of the ultrasound-scanning light source in opsin-expressing neurons through electrophysiological recordings and immunostaining. We showcase dynamic three-dimensional brain targeting and temporally resolved behavioral control in freely moving animals via the ultrasound-scanning in vivo light source. This non-invasive deep-tissue light source offers a versatile strategy for body-wide optical interfacing.

## Full-text entities

- **Genes:** Iba1 (induction of brown adipocytes 1) [NCBI Gene 114737], Eif1a (eukaryotic translation initiation factor 1A) [NCBI Gene 13664] {aka Ef1a, Eftu, Eif4c, eIF-1A, eIF-4C}, Fus (fused in sarcoma) [NCBI Gene 233908] {aka D430004D17Rik, D930039C12Rik, Fus1, Tls}, Gfap (glial fibrillary acidic protein) [NCBI Gene 14580], Thy1 (thymus cell antigen 1, theta) [NCBI Gene 21838] {aka CD90, T25, Thy-1, Thy-1.2, Thy1.1, Thy1.2}, Rpa1 (replication protein A1) [NCBI Gene 68275] {aka 5031405K23Rik, 70kDa, RF-A, RP-A, Rpa}, Fos (Fos proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 14281] {aka D12Rfj1, c-fos, cFos}
- **Diseases:** hypothermia (MESH:D007035), inflammation (MESH:D007249), neuroinflammation (MESH:D000090862), toxicity (MESH:D064420), necrosis (MESH:D009336)
- **Chemicals:** Au (MESH:D006046), H&amp;E (MESH:D006371), LED (-), paraffin (MESH:D010232), hematoxylin (MESH:D006416), Eu (MESH:D005063), lead zirconate titanate (MESH:C065536), xylazine (MESH:D014991), Cr (MESH:D002857), Dy (MESH:D004419), dexdomitor (MESH:D020927), Epoxy (MESH:D004853), Triton X-100 (MESH:D017830), PDMS (MESH:C013830), water (MESH:D014867), chloroform (MESH:D002725), zirconia (MESH:C028541), PFA (MESH:C003043), sucrose (MESH:D013395), isoflurane (MESH:D007530), copper (MESH:D003300), silicone (MESH:D012828), eosin (MESH:D004801), tungsten carbide (MESH:C002802), oleic acid (MESH:D019301), Parylene C (MESH:C011055), HNO3 (MESH:D017942)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** H134R
- **Cell lines:** C57BL/6J — Mus musculus (Mouse), Transformed cell line (CVCL_C0MW), /6J — Homo sapiens (Human), Cutaneous melanoma, Cancer cell line (CVCL_W797)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12204340/full.md

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Source: https://tomesphere.com/paper/PMC12204340