4.8 Article

Quantitatively Monitoring In Situ Mitochondrial Thermal Dynamics by Upconversion Nanoparticles

期刊

NANO LETTERS
卷 21, 期 4, 页码 1651-1658

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.nanolett.0c04281

关键词

Upconversion Nanoparticles (UCNPs); Biosensing; Nanothermometry; Mitochondria

资金

  1. Australia National Health and Medical Council (NHMRC) [APP1177374]
  2. Australia National Heart Foundation (NHF) [102592]
  3. Australian Research Council Discovery Early Career Researcher Award Scheme [DE180100669]
  4. National Natural Science Foundation of China (NSFC) [61729501]
  5. Major International (Regional) Joint Research Project of NSFC [51720105015]
  6. Science and Technology Innovation Commission of Shenzhen [KQTD20170810110913065]
  7. Australia China Science and Research Fund Joint Research Centre for Point-of-Care Testing [ACSRF658277, SQ2017YFGH001190]
  8. China Scholarship Council [201706170028, 201706170027]

向作者/读者索取更多资源

The study presents an upconversion nanoparticle-based thermometer for real-time monitoring of mitochondrial temperature in living cells, which shows independent temperature-responsive feature from probe concentration and medium conditions. This technology has the potential applications in studying mitochondrial metabolism pathways and organelle interactions through measuring temperature difference under various stimulations. Cells exhibit distinct response time and thermodynamic profiles under different conditions, showcasing the versatility of this thermometer in studying vital processes related to mitochondria.
Temperature dynamics reflect the physiological conditions of cells and organisms. Mitochondria regulate the temperature dynamics in living cells as they oxidize the respiratory substrates and synthesize ATP, with heat being released as a byproduct of active metabolism. Here, we report an upconversion nanoparticle-based thermometer that allows the in situ thermal dynamics monitoring of mitochondria in living cells. We demonstrate that the upconversion nanothermometers can efficiently target mitochondria, and the temperature-responsive feature is independent of probe concentration and medium conditions. The relative sensing sensitivity of 3.2% K-1 in HeLa cells allows us to measure the mitochondrial temperature difference through the stimulations of high glucose, lipid, Ca2+ shock, and the inhibitor of oxidative phosphorylation. Moreover, cells display distinct response time and thermodynamic profiles under different stimulations, which highlight the potential applications of this thermometer to study in situ vital processes related to mitochondrial metabolism pathways and interactions between organelles.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据