Lipid droplets as endogenous intracellular microlenses

An optically trapped lipid droplet inside an adipose cell focuses the excitation light and collects the fluorescent signals from the cytoskeleton to form a magnified fluorescence image.
Credit by Xixi Chen, Tianli Wu, Zhiyong Gong, Jinghui Guo, Xiaoshuai Liu, Yao Zhang, Yuchao Li, Pietro Ferraro, and Baojun Li

With the demand in real-time monitoring of endoplasmic variations and rapid detection of extracellular signals, a great number of approaches to bioimaging have been developed. The past few decades have witnessed a dramatic progress in optical imaging, especially with the emerging of microsphere-assisted techniques that have the excellent ability of signal collection and enable real-time and super-resolution imaging with conventional optical microscopic systems.

However, as most of the microspheres in current strategies are in solid and artificially synthetic materials, they are of very low biocompatibility. Fortunately, lessons from nature have shown that some bio-components and already-existing objects can interact with light and are able to take the same functions as the real optical elements.

In a paper newly published in Light Science & Application, a team of researchers, led by Professors Baojun Li, Yao Zhang and Yuchao Li from Institute of Nanophotonics, Jinan University, China and Dr. Pietro Ferraro from CNR-ISASI, Institute of Applied Sciences and Intelligent Systems, Italy, demonstrate that lipid droplets, a sort of dynamic structures that naturally exist in cells, can act as intracellular microlenses for real-time monitoring of subcellular structures and detection of extracellular signals. With a spherical shape and a refractive index higher than cytoplasm and periplasm, the lipid droplets exhibit the lensing effect to efficiently converge both the excitation light and the fluorescence signals (Figure 1).

(a) Fluorescence images of the microfilaments (F-actin filaments) of a living adipose cell. The weak fluorescent signals (a1) were efficiently enhanced by the lipid droplet (diameter: 7.7 μm) (a2). (b) Fluorescence images of the microfilaments in a fixed adipose cell with an 18.6-μm lipid droplet. (c) Fluorescence and bright-field images of the lysosomes in a living adipose cell with an 11.3-μm lipid droplet. (d) Fluorescence and bright-field images of the adenoviruses in a living adipose cell with an 8.1-μm lipid droplet, the blue lines represent the movement trajectory of the adenoviruses in 10 min. The fluorescence images were focused on the surfaces of the cells (b1) and the virtual image planes (b2, c1 and d1) formed by the lipid droplets. The bright-field image was focused on the virtual image plane formed by the lipid droplet (c2 and d2).
Credit by Xixi Chen, Tianli Wu, Zhiyong Gong, Jinghui Guo, Xiaoshuai Liu, Yao Zhang, Yuchao Li, Pietro Ferraro, and Baojun Li

To achieve intracellular imaging of subcellular structures, the lipidic microlenses work in a contact mode in which the collection efficiency of the emitted fluorescent signals was greatly increased by the lipid droplets.

As a result, the required excitation power in fluorescence imaging can be reduced by up to 73%. Driven by scanning optical tweezers, the lipid droplets can be moved inside the cell to perform an enhanced intracellular fluorescence imaging of the microfilaments, lysosomes and adenoviruses in living cells (Figure 2).

Moreover, due to the refractive index contrast of the lipid droplets to cytoplasm, the long focal length of the lipid droplets can extend the fluorescence enhancement strategies to a non-contact mode that increases the working distance of imaging and detection by the lipidic microlenses.

(a) Schematic (side view) of the enhanced detection of cancer cells in fluid by a lipid droplet inside the adipose cell: the lipid droplet acts as a biolens by focusing excitation light into the cancer cell and improving the collection of fluorescent signals at same time. (b) Fluorescence images (top view) of the detecting process. The yellow and red dotted circles indicate the lipid droplet (diameter: 20 μm) and the cancer cell, respectively. The mitochondria of the cancer cell were marked by Mito-Tracker (green). The red arrow indicates the direction of fluid flow in the capillary.
Credit by Xixi Chen, Tianli Wu, Zhiyong Gong, Jinghui Guo, Xiaoshuai Liu, Yao Zhang, Yuchao Li, Pietro Ferraro, and Baojun Li

In the non-contact mode, the excitation light was highly converged by the lipid droplets to enhance the fluorescence intensity from the extracellular environment surrounding the cells.

In the experiments, an efficient detecting of fluorescent signals of cancer cells in extracellular fluid was accomplished by the lipidic microlenses (Figure 3).

The presented lensing effect of the lipid droplets is expected to find applications to fully biocompatible miniaturized tools for biosensing, endoscopic analysis and single-cell diagnosis.

The use of the lipid droplets as intracellular microlenses also provides opportunities to design and construct diverse endogenous photonic devices.

DOI: 10.1038/s41377-021-00687-3
Article Title: Lipid droplets as endogenous intracellular microlenses
Article Publication Date: 6-Dec-2021

Media Contact

Yaobiao Li
Light Publishing Center, Changchun Institute of Optics, Fine Mechanics And Physics, CAS
Office: 86-431-861-76851

Expert Contact

Baojun Li
Jinan University

Media Contact

Yaobiao Li
Light Publishing Center, Changchun Institute of Optics, Fine Mechanics And Physics, CAS

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