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A quadrupolar two-photon fluorescent probe for in vivo imaging of amyloid-β plaques
The formation of beta amyloid (Aβ) plaques in specific brain regions is one of the early pathological hallmarks of Alzheimer's disease (AD). To enable the early detection of AD and related applications, a method for real-time, clear 3D visualization of Aβ plaques in vivo is highly desirable. Tw...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6016450/ https://www.ncbi.nlm.nih.gov/pubmed/30155107 http://dx.doi.org/10.1039/c6sc00355a |
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author | Heo, Cheol Ho Sarkar, Avik Ranjan Baik, Sung Hoon Jung, Tae Sung Kim, Jeong Jin Kang, Hyuk Mook-Jung, Inhee Kim, Hwan Myung |
author_facet | Heo, Cheol Ho Sarkar, Avik Ranjan Baik, Sung Hoon Jung, Tae Sung Kim, Jeong Jin Kang, Hyuk Mook-Jung, Inhee Kim, Hwan Myung |
author_sort | Heo, Cheol Ho |
collection | PubMed |
description | The formation of beta amyloid (Aβ) plaques in specific brain regions is one of the early pathological hallmarks of Alzheimer's disease (AD). To enable the early detection of AD and related applications, a method for real-time, clear 3D visualization of Aβ plaques in vivo is highly desirable. Two-photon microscopy (TPM) which utilizes two near-infrared photons is an attractive tool for such applications. However, this technique needs a sensitive and photostable two-photon (TP) probe possessing bright TP exited fluorescence to impart high signal-to-noise (S/N) visualization of Aβ plaques. Herein, we report a quadrupolar TP fluorescent probe (QAD1) having large TP action cross section (Φδ(max) = 420 GM) and its application for in vivo TPM imaging of Aβ plaques. This probe, designed with a centrosymmetric D–A–D motif with a cyclic conjugating bridge and solubilizing unit, displays bright TP excited fluorescence, appreciable water solubility, robust photostability, and high sensitivity and selectivity for Aβ plaques. Using the real-time TPM imaging of transgenic 5XFAD mice after intravenous injection of QAD1, we show that this probe readily enters the blood brain barrier and provides high S/N ratio images of individual Aβ plaques in vivo. We also used QAD1 in dual-color TPM imaging for 3D visualization of Aβ plaques along with blood vessels and cerebral amyloid angiopathy (CAA) inside living mouse brains. These findings demonstrate that this probe will be useful in biomedical applications including early diagnosis and treatments of AD. |
format | Online Article Text |
id | pubmed-6016450 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-60164502018-08-28 A quadrupolar two-photon fluorescent probe for in vivo imaging of amyloid-β plaques Heo, Cheol Ho Sarkar, Avik Ranjan Baik, Sung Hoon Jung, Tae Sung Kim, Jeong Jin Kang, Hyuk Mook-Jung, Inhee Kim, Hwan Myung Chem Sci Chemistry The formation of beta amyloid (Aβ) plaques in specific brain regions is one of the early pathological hallmarks of Alzheimer's disease (AD). To enable the early detection of AD and related applications, a method for real-time, clear 3D visualization of Aβ plaques in vivo is highly desirable. Two-photon microscopy (TPM) which utilizes two near-infrared photons is an attractive tool for such applications. However, this technique needs a sensitive and photostable two-photon (TP) probe possessing bright TP exited fluorescence to impart high signal-to-noise (S/N) visualization of Aβ plaques. Herein, we report a quadrupolar TP fluorescent probe (QAD1) having large TP action cross section (Φδ(max) = 420 GM) and its application for in vivo TPM imaging of Aβ plaques. This probe, designed with a centrosymmetric D–A–D motif with a cyclic conjugating bridge and solubilizing unit, displays bright TP excited fluorescence, appreciable water solubility, robust photostability, and high sensitivity and selectivity for Aβ plaques. Using the real-time TPM imaging of transgenic 5XFAD mice after intravenous injection of QAD1, we show that this probe readily enters the blood brain barrier and provides high S/N ratio images of individual Aβ plaques in vivo. We also used QAD1 in dual-color TPM imaging for 3D visualization of Aβ plaques along with blood vessels and cerebral amyloid angiopathy (CAA) inside living mouse brains. These findings demonstrate that this probe will be useful in biomedical applications including early diagnosis and treatments of AD. Royal Society of Chemistry 2016-07-01 2016-04-07 /pmc/articles/PMC6016450/ /pubmed/30155107 http://dx.doi.org/10.1039/c6sc00355a Text en This journal is © The Royal Society of Chemistry 2016 https://creativecommons.org/licenses/by/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0) |
spellingShingle | Chemistry Heo, Cheol Ho Sarkar, Avik Ranjan Baik, Sung Hoon Jung, Tae Sung Kim, Jeong Jin Kang, Hyuk Mook-Jung, Inhee Kim, Hwan Myung A quadrupolar two-photon fluorescent probe for in vivo imaging of amyloid-β plaques |
title | A quadrupolar two-photon fluorescent probe for in vivo imaging of amyloid-β plaques
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title_full | A quadrupolar two-photon fluorescent probe for in vivo imaging of amyloid-β plaques
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title_fullStr | A quadrupolar two-photon fluorescent probe for in vivo imaging of amyloid-β plaques
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title_full_unstemmed | A quadrupolar two-photon fluorescent probe for in vivo imaging of amyloid-β plaques
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title_short | A quadrupolar two-photon fluorescent probe for in vivo imaging of amyloid-β plaques
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title_sort | quadrupolar two-photon fluorescent probe for in vivo imaging of amyloid-β plaques |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6016450/ https://www.ncbi.nlm.nih.gov/pubmed/30155107 http://dx.doi.org/10.1039/c6sc00355a |
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