In vivo three-dimensional brain imaging with chemiluminescence probes in Alzheimer’s disease models

Author:

Zhang Jing1ORCID,Wickizer Carly2ORCID,Ding Weihua3,Van Richard2ORCID,Yang Liuyue3,Zhu Biyue1,Yang Jun1ORCID,Wang Yanli1ORCID,Wang Yongle1,Xu Yulong1,Zhang Can4,Shen Shiqian3,Wang Changning1,Shao Yihan2,Ran Chongzhao1ORCID

Affiliation:

1. Department of Radiology, Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Charlestown, Boston, MA 02129

2. Department of Chemistry and Biochemistry, Stephenson Life Sciences Research Center, University of Oklahoma, Norman, OK 73019

3. Department of Anesthesia Critical Care and Pain Medicine, MGH Center for Translational Pain Research, Massachusetts General Hospital Harvard Medical School, Boston, MA 02114

4. Genetics and Aging Research Unit, Department of Neurology, McCance Center for Brain Health Mass General Institute for Neurodegenerative Disease, Massachusetts General Hospital Harvard Medical School, Charlestown, MA 02129

Abstract

Optical three-dimensional (3D) molecular imaging is highly desirable for providing precise distribution of the target-of-interest in disease models. However, such 3D imaging is still far from wide applications in biomedical research; 3D brain optical molecular imaging, in particular, has rarely been reported. In this report, we designed chemiluminescence probes with high quantum yields, relatively long emission wavelengths, and high signal-to-noise ratios to fulfill the requirements for 3D brain imaging in vivo. With assistance from density-function theory (DFT) computation, we designed ADLumin-Xs by locking up the rotation of the double bond via fusing the furan ring to the phenyl ring. Our results showed that ADLumin-5 had a high quantum yield of chemiluminescence and could bind to amyloid beta (Aβ). Remarkably, ADLumin-5’s radiance intensity in brain areas could reach 4 × 10 7 photon/s/cm 2 /sr, which is probably 100-fold higher than most chemiluminescence probes for in vivo imaging. Because of its strong emission, we demonstrated that ADLumin-5 could be used for in vivo 3D brain imaging in transgenic mouse models of Alzheimer’s disease.

Funder

HHS | National Institutes of Health

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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