Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Heo, Cheol Ho, Sarkar, Avik Ranjan, Baik, Sung Hoon, Jung, Tae Sung, Kim, Jeong Jin, Kang, Hyuk, Mook-Jung, Inhee, Kim, Hwan Myung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2016
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
_version_ 1783334574201241600
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
title_full A quadrupolar two-photon fluorescent probe for in vivo imaging of amyloid-β plaques
title_fullStr A quadrupolar two-photon fluorescent probe for in vivo imaging of amyloid-β plaques
title_full_unstemmed A quadrupolar two-photon fluorescent probe for in vivo imaging of amyloid-β plaques
title_short A quadrupolar two-photon fluorescent probe for in vivo imaging of amyloid-β plaques
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
work_keys_str_mv AT heocheolho aquadrupolartwophotonfluorescentprobeforinvivoimagingofamyloidbplaques
AT sarkaravikranjan aquadrupolartwophotonfluorescentprobeforinvivoimagingofamyloidbplaques
AT baiksunghoon aquadrupolartwophotonfluorescentprobeforinvivoimagingofamyloidbplaques
AT jungtaesung aquadrupolartwophotonfluorescentprobeforinvivoimagingofamyloidbplaques
AT kimjeongjin aquadrupolartwophotonfluorescentprobeforinvivoimagingofamyloidbplaques
AT kanghyuk aquadrupolartwophotonfluorescentprobeforinvivoimagingofamyloidbplaques
AT mookjunginhee aquadrupolartwophotonfluorescentprobeforinvivoimagingofamyloidbplaques
AT kimhwanmyung aquadrupolartwophotonfluorescentprobeforinvivoimagingofamyloidbplaques
AT heocheolho quadrupolartwophotonfluorescentprobeforinvivoimagingofamyloidbplaques
AT sarkaravikranjan quadrupolartwophotonfluorescentprobeforinvivoimagingofamyloidbplaques
AT baiksunghoon quadrupolartwophotonfluorescentprobeforinvivoimagingofamyloidbplaques
AT jungtaesung quadrupolartwophotonfluorescentprobeforinvivoimagingofamyloidbplaques
AT kimjeongjin quadrupolartwophotonfluorescentprobeforinvivoimagingofamyloidbplaques
AT kanghyuk quadrupolartwophotonfluorescentprobeforinvivoimagingofamyloidbplaques
AT mookjunginhee quadrupolartwophotonfluorescentprobeforinvivoimagingofamyloidbplaques
AT kimhwanmyung quadrupolartwophotonfluorescentprobeforinvivoimagingofamyloidbplaques