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用于细胞脂滴超分辨荧光成像的有机荧光探针研究进展

周日,王晨光,卢革宇

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周日, 王晨光, 卢革宇. 用于细胞脂滴超分辨荧光成像的有机荧光探针研究进展[J]. , 2022, 15(6): 1228-1242. doi: 10.37188/CO.2022-0077
引用本文: 周日, 王晨光, 卢革宇. 用于细胞脂滴超分辨荧光成像的有机荧光探针研究进展[J]. , 2022, 15(6): 1228-1242.doi:10.37188/CO.2022-0077
ZHOU Ri, WANG Chen-guang, LU Ge-yu. Advances in organic fluorescent probes for super-resolution imaging of cellular lipid droplets[J]. Chinese Optics, 2022, 15(6): 1228-1242. doi: 10.37188/CO.2022-0077
Citation: ZHOU Ri, WANG Chen-guang, LU Ge-yu. Advances in organic fluorescent probes for super-resolution imaging of cellular lipid droplets[J].Chinese Optics, 2022, 15(6): 1228-1242.doi:10.37188/CO.2022-0077

用于细胞脂滴超分辨荧光成像的有机荧光探针研究进展

doi:10.37188/CO.2022-0077
基金项目:国家自然科学基金(No. 61831011,No. 62075079)
详细信息
    作者简介:

    周 日(1992—),男,吉林德惠人,博士,2021年于吉林大学获得博士学位,主要从事细胞脂滴荧光探针的研制及其STED超分辨成像研究。E-mail:126144029@qq.com

    王晨光(1988—),男,安徽利辛人,教授,博士生导师,2013年于吉林大学获得博士学位,主要从事有机荧光探针的研制及其STED超分辨成像研究。E-mail:wangchenguang@jlu.edu.cn

    卢革宇(1963—),男,黑龙江海伦人,教授,博士生导师,1998年于日本九州大学获得博士学位,主要从事传感器、光电子材料与器件、物联网和微纳传感系统等方面的研究。E-mail:lugy@jlu.edu.cn

  • 中图分类号:O652.7;O439

Advances in organic fluorescent probes for super-resolution imaging of cellular lipid droplets

Funds:Supported by National Natural Science Foundation of China (No. 61831011, No. 62075079)
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  • 摘要:

    脂滴是真核细胞中必不可少的一种球形细胞器,与很多细胞生理学过程息息相关。荧光成像技术是观察研究脂滴最有力的工具之一。受光学衍射极限的限制,传统的宽场以及共聚焦显微镜所能达到的成像分辨率约为250 nm左右,这对于观测小脂滴,尤其是新生脂滴(尺寸约30~60 nm)来说是远远不够的。在这种情况下,近年来新兴的各种能够打破衍射极限的超分辨荧光显微镜(如受激发射损耗显微镜、结构光照明显微镜以及光激活定位显微镜等)逐渐吸引了科研人员的兴趣。为了得到高分辨率脂滴荧光图像,除了上述超分辨显微镜之外,还需要具有与之相匹配的高性能荧光探针。本文将简要介绍这几种超分辨显微镜的工作原理,讨论其对荧光探针光物理性质的特殊要求,并进一步系统总结脂滴超分辨成像荧光探针的研究进展。与此同时,本文将分析对比不同超分辨显微镜在脂滴荧光成像方面的优势与不足,并对其发展趋势进行展望。

  • 图 1STED超分辨显微镜原理

    Figure 1.The principle of the STED super-resolution microscope

    图 2用于脂滴STED超分辨成像的有机荧光探针

    Figure 2.The organic fluorescent probes for STED super-resolution imaging of lipid droplets

    图 3脂滴荧光探针LAQ1在多色共聚焦成像和STED超分辨成像中的应用。(a)脂滴、内质网和线粒体的三色荧光成像;(b)穿过白色箭头的信号强度分布;(c)小脂滴的STED成像;(d)穿过同一小脂滴的共聚焦和STED成像信号强度图[19]

    Figure 3.The applications of lipid droplets fluorescent probe LAQ1 in multicolor confocal imaging and STED super-resolution imaging. (a) Three-color fluorescence imaging of lipid droplets, endoplasmic reticulum and mitochondria; (b) signal intensity profiles across the white arrow; (c) STED imaging of lipid droplets; (d) confocal and STED imaging signal intensity profiles across the same lipid droplet[19]

    图 4脂滴荧光探针DTPA-BT-M在(a)STED超分辨和(b)双光子成像中的应用[20]

    Figure 4.The applications of lipid droplets fluorescent probe DTPA-BT-M in (a) STED super-resolution and (b) two-photon imaging[20]

    图 5脂滴荧光探针Lipi-DSB的STED超分辨成像。(a)损耗 功率依赖的分辨率;(b)与线粒体荧光探针四甲基罗丹明搭配的双色STED成像;(c)连续1000帧的STED超分辨成像动态跟踪;(d)STED超分辨成像动态跟踪纳米尺度新生脂滴的融合过程[21]

    Figure 5.STED super-resolution imaging of lipid droplets fluorescent probe Lipi-DSB. (a) STED laser power-dependent resolution; (b) two-color STED imaging of Lipi-DSB paired with mitochondria fluorescent probe tetramethylrhodamine; (c) time-lapse STED super-resolution imaging (1000 consecutive frames); (d) dynamic tracking of nascent lipid droplet fusion processes at the nanoscale by STED super-resolution imaging[21]

    图 6脂滴荧光探针Lipi-BDTO的共聚焦和STED超分辨成像。(a)共聚焦和STED成像对比;(b)3D STED成像[22]

    Figure 6.Confocal and STED super-resolution imaging of the lipid droplets fluorescent probe Lipi-BDTO. (a) Comparison of confocal and STED imaging; (b) 3D STED imaging[22]

    图 7SIM超分辨成像原理[64]

    Figure 7.The principle of SIM super-resolution microscope[64]

    图 8用于脂滴SIM超分辨成像的有机荧光探针

    Figure 8.The organic fluorescent probes for SIM super-resolution imaging of lipid droplets

    图 9脂滴荧光探针LD-FG的SIM超分辨成像。(a)缓冲策略提升光稳定性;(b)荧光探针的光开关特性;(c)相邻脂滴间的融合;(d)不相邻脂滴间的融合[27]

    Figure 9.SIM super-resolution imaging of the lipid droplets fluorescent probe LD-FG. (a) Buffer strategy enables stable imaging of lipid droplets; (b) fluorescence switching property of the fluorescent probe; (c) coalescence between adjacent lipid droplets; (d) coalescence between non-adjacent lipid droplets[27]

    图 10有机荧光探针在脂滴SIM超分辨成像中的应用。(a)荧光探针DTZ-TPA-DCN用于染色核脂滴[28];(b)荧光探针NIM-3A用于分析细胞内脂滴数量和尺寸[29];(c)荧光探针NIM-7用于追踪脂滴和溶酶体的动态过程[30]

    Figure 10.Applications of organic fluorescent probes in SIM super-resolution imaging of lipid droplets. (a) Fluorescent probe DTZ-TPA-DCN used for staining nuclear lipid droplets[28]; (b) fluorescent probe NIM-3A used for analyzing the number and size of lipid droplets[29]; (c) fluorescent probe NIM-7 used for tracking dynamic processes of lipid droplets and lysosomes[30]

    图 11分子定位技术原理示意图[68]

    Figure 11.Schematic diagram of molecular localization technology[68]

    图 12光开关荧光探针在脂滴PALM超分辨成像中的应用。(a)具有荧光开关特性的有机荧光探针;(b)脂肪细胞中脂滴在宽场和PALM显微镜下的明场和双色成像[31]

    Figure 12.Applications of light-switchable fluorescent probes in PALM super-resolution imaging of lipid droplets. (a) The organic fluorescent probes with fluorescence ON/OFF characteristics; (b) bright field and two-color imaging of lipid droplets in adipocyte under wide-field and PALM microscopes[31]

    表 1文献中报道的细胞脂滴超分辨成像结果总结

    Table 1.Summary of super-resolution imaging of cell lipid droplets reported in the literatures

    发表年份 超分辨成像技术 荧光探针 成像分辨率/nm 是否动态超分辨成像 参考文献
    2021 STED LAQ1 166 未提及 19
    2021 STED DTPA-BT-M 95 未提及 20
    2021 STED Lipi-DSB 58 21
    2021 STED Lipi-BDTO 65 22
    2021 SIM LD-FG 180 27
    2021 SIM DTZ-TPA-DCN 未提及 未提及 28
    2018 SIM NIM-3A 未提及 未提及 29
    2019 SIM NIM-7 未提及 未提及 30
    2019 PALM SNile Red <250 未提及 31
    2021 PALM BAD-Oxm 未提及 未提及 32
    2020 PALM BODIPY-C12 125 未提及 33
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  • 收稿日期:2022-04-22
  • 修回日期:2022-05-07
  • 网络出版日期:2022-06-20

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