An optical nanoreporter of endolysosomal lipid accumulation reveals enduring effects of diet on hepatic macrophages in vivo

被引:85
作者
Galassi, Thomas V. [1 ,2 ]
Jena, Prakrit V. [1 ]
Shah, Janki [1 ]
Ao, Geyou [3 ]
Molitor, Elizabeth [4 ]
Bram, Yaron [2 ]
Frankel, Angela [2 ]
Park, Jiwoon [2 ]
Jessurun, Jose [2 ]
Ory, Daniel S. [4 ]
Haimovitz-Friedman, Adriana [1 ]
Roxbury, Daniel [5 ]
Mittal, Jeetain [6 ]
Zheng, Ming [3 ]
Schwartz, Robert E. [2 ]
Heller, Daniel A. [1 ,2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, New York, NY 10065 USA
[2] Weill Cornell Med, New York, NY 10065 USA
[3] Natl Inst Stand & Technol, Gaithersburg, MD 20899 USA
[4] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[5] Univ Rhode Isl, Dept Chem Engn, Kingston, RI 02881 USA
[6] Lehigh Univ, Dept Chem & Biomol Engn, Bethlehem, PA 18015 USA
基金
美国国家科学基金会;
关键词
WALLED CARBON NANOTUBES; DRUG-INDUCED PHOSPHOLIPIDOSIS; NIEMANN-PICK-DISEASE; FATTY LIVER-DISEASE; SINGLE-STRANDED-DNA; NONALCOHOLIC STEATOHEPATITIS; MOLECULAR-DYNAMICS; CELLS; MODEL; MICE;
D O I
10.1126/scitranslmed.aar2680
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The abnormal accumulation of lipids within the endolysosomal lumen occurs in many conditions, including lysosomal storage disorders, atherosclerosis, nonalcoholic fatty liver disease (NAFLD), and drug-induced phospholipidosis. Current methods cannot monitor endolysosomal lipid content in vivo, hindering preclinical drug development and research into the mechanisms linking endolysosomal lipid accumulation to disease progression. We developed a single-walled carbon nanotube-based optical reporter that noninvasively measures endolysosomal lipid accumulation via bandgap modulation of its intrinsic near-infrared emission. The reporter detected lipid accumulation in Niemann-Pick disease, atherosclerosis, and NAFLD models in vivo. By applying the reporter to the study of NAFLD, we found that elevated lipid quantities in hepatic macrophages caused by a high-fat diet persist long after reverting to a normal diet. The reporter dynamically monitored endolysosomal lipid accumulation in vivo over time scales ranging from minutes to weeks, indicating its potential to accelerate preclinical research and drug development processes.
引用
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页数:10
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