Ultrabright and Fluorogenic Probes for Multicolor Imaging and Tracking of Lipid Droplets in Cells and Tissues

被引:416
作者
Collot, Mayeul [1 ]
Fam, Tkhe Kyong [1 ]
Ashokkumar, Pichandi [1 ]
Faklaris, Orestis [2 ]
Galli, Thierry [3 ,4 ]
Danglot, Lydia [3 ,4 ]
Klymchenko, Andrey S. [1 ]
机构
[1] Univ Strasbourg, CNRS UMR 7213, Lab Biophoton & Pharmacol, Fac Pharm, 74 Route Rhin, F-67401 Illkirch Graffenstaden, France
[2] Univ Paris Diderot, CNRS, ImagoSeine Core Facil, Inst Jacques Monod,UMR 7593, 15 Rue Helene Brion, F-75205 Paris 13, France
[3] INSERM U894, Ctr Psychiat & Neurosci, Membrane Traff Hlth & Diseased Brain Team, 102-108 Rue Sante, F-75014 Paris, France
[4] Univ Paris 05, F-75014 Paris, France
基金
欧洲研究理事会;
关键词
2-PHOTON EXCITATION MICROSCOPY; FLUORESCENT-PROBES; POLYMETHINE DYES; BULKY SUBSTITUENTS; SOLID-STATE; RED; POLYLACTIDE; EMISSION; FLUOROPHORES; DIOXABORINE;
D O I
10.1021/jacs.7b12817
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Lipid droplets (LDs) are intracellular lipid-rich organelles that regulate the storage of neutral lipids and were recently found to be involved in many physiological processes, metabolic disorders, and diseases including obesity, diabetes, and cancers. Herein we present a family of new fluorogenic merocyanine fluorophores based on an indolenine moiety and a dioxaborine barbiturate derivative. These so-called StatoMerocyanines (SMCy) fluoresce from yellow to the near-infrared (NIR) in oil with an impressive fluorescence enhancement compared to aqueous media. Additionally, SMCy display remarkably high molar extinction coefficients (up to 390 000 M-1 cm(-1)) and high quantum yield values (up to 100%). All the members of this new family specifically stain the LDs in live cells with very low background noise. Unlike Nile Red, a well-known lipid droplet marker, SMCy dyes possess narrow absorption and emission bands in the visible, thus allowing multicolor imaging. SMCy proved to be compatible with fixation and led to high-quality 3D images of lipid droplets in cells and tissues. Their high brightness allowed efficient tissue imaging of adipocytes and circulating LDs. Moreover their remarkably high two-photon absorption cross-section, especially SMCy5.5 (up to 13 300 GM), as well as their capacity to efficiently fluoresce in the NIR region led to two-photon multicolor tissue imaging (liver). Taking advantage of the available color palette, lipid droplet exchange between cells was tracked and imaged, thus demonstrating intercellular communication.
引用
收藏
页码:5401 / 5411
页数:11
相关论文
共 74 条
[1]
The role of lipid droplets and adipocytes in cancer. Raman imaging of cell cultures: MCF10A, MCF7, and MDA-MB-231 compared to adipocytes in cancerous human breast tissue [J].
Abramczyk, Halina ;
Surmacki, Jakub ;
Kopec, Monika ;
Olejnik, Alicja Klaudia ;
Lubecka-Pietruszewska, Katarzyna ;
Fabianowska-Majewska, Krystyna .
ANALYST, 2015, 140 (07) :2224-2235
[2]
Two-photon fluorescence excitation cross sections of biomolecular probes from 690 to 960 nm [J].
Albota, MA ;
Xu, C ;
Webb, WW .
APPLIED OPTICS, 1998, 37 (31) :7352-7356
[3]
Rhodamine 800 as reference substance for fluorescence quantum yield measurements in deep red emission range [J].
Alessi, A. ;
Salvalaggio, M. ;
Ruzzon, G. .
JOURNAL OF LUMINESCENCE, 2013, 134 :385-389
[4]
[Anonymous], 2006, M86 E01078 APEX2 USE
[5]
Specific Imaging of Intracellular Lipid Droplets Using a Benzothiadiazole Derivative with Solvatochromic Properties [J].
Appelqvist, Hanna ;
Stranius, Kati ;
Borjesson, Karl ;
Nilsson, K. Peter. R. ;
Dyrager, Christine .
BIOCONJUGATE CHEMISTRY, 2017, 28 (05) :1363-1370
[6]
FLUORESCENCE PROPERTIES OF INDOCYANINE GREEN AS RELATED TO ANGIOGRAPHY [J].
BENSON, RC ;
KUES, HA .
PHYSICS IN MEDICINE AND BIOLOGY, 1978, 23 (01) :159-163
[7]
Synthesis and Biosynthetic Trafficking of Membrane Lipids [J].
Blom, Tomas ;
Somerharju, Pentti ;
Ikonen, Elina .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2011, 3 (08) :1-16
[8]
Lipid droplets in inflammation and cancer [J].
Bozza, Patricia T. ;
Viola, Joao P. B. .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 2010, 82 (4-6) :243-250
[9]
Chan J, 2012, NAT CHEM, V4, P973, DOI [10.1038/NCHEM.1500, 10.1038/nchem.1500]
[10]
Second harmonic generation microscopy for quantitative analysis of collagen fibrillar structure [J].
Chen, Xiyi ;
Nadiarynkh, Oleg ;
Plotnikov, Sergey ;
Campagnola, Paul J. .
NATURE PROTOCOLS, 2012, 7 (04) :654-669