Live Cell Labeling of Glial Progenitor Cells Using Targeted Quantum Dots

被引:8
作者
Sabharwal, Nidhi [1 ]
Holland, Eric C. [2 ,3 ,4 ]
Vazquez, Maribel [1 ]
机构
[1] CUNY City Coll, Dept Biomed Engn, New York, NY 10031 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Neurosurg, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Neurol, New York, NY 10021 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Cell Biol, New York, NY 10021 USA
关键词
Quantum dots; Platelet derived growth factor; Glial progenitor cells; Live cell labeling; Cationic liposome; GROWTH-FACTOR PDGF; IN-VIVO; OLIGODENDROGLIOMAS; DELIVERY; ASTROCYTOMAS; CANCER; PROBES;
D O I
10.1007/s10439-009-9703-4
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
This study describes the development of targeted quantum dots (T-QDs) as biomarkers for the labeling of glial progenitor cells (GPCs) that over express platelet derived growth factor (PDGF) and its receptor PDGFR (GPC(PDGF)). PDGFR plays a critical role in glioma development and growth, and is also known to affect multiple biological processes such as cell migration and embryonic development. T-QDs were developed using streptavidin-conjugated quantum dots (S-QDs) with biotinylated antibodies and utilized to label the intracellular and extracellular domains of live, cultured GPC(PDGF) cells via lipofection with cationic liposomes. Confocal studies illustrate successful intracellular and extracellular targeted labeling within live cells that does not appear to impact upstream PDGFR dynamics during real-time signaling events. Further, T-QDs were nontoxic to GPC(PDGF) cells, and did not alter cell viability or proliferation over the course of 6 days. These results raise new applications for T-QDs as ultra sensitive agents for imaging and tracking of protein populations within live cells, which that will enable future mechanistic study of oncogenic signaling events in real-time.
引用
收藏
页码:1967 / 1973
页数:7
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