Inorganic fluorescent nanoprobes for cellular and subcellular imaging

TrAC - Trends in Analytical Chemistry

Volumn 58, Issue , 2014, Pages 120-129

  Chen, Mian ^a   He, Xiaoxiao ^a   Wang, Kemin ^a   He, Dinggeng ^a   Yang, Xiaohai ^a   Shi, Hui ^a  

^a HUNAN UNIVERSITY   (China)

Author keywords

Cellular imaging; Cellular uptake; Cytotoxicity; Dye containing silica nanoparticle; Fluorescent nanoprobe; Inorganic nanoprobe; Metal nanocluster; Quantum dot; Subcellular imaging; Upconversion nanoparticle

Indexed keywords

BIOCHEMISTRY; CYTOTOXICITY; FLUORESCENCE; METAL NANOPARTICLES; NANOCLUSTERS; SEMICONDUCTOR QUANTUM DOTS;

CELLULAR IMAGING; CELLULAR UPTAKE; METAL NANOCLUSTERS; QUANTUM DOT; SILICA NANOPARTICLES; SUB-CELLULAR; UPCONVERSION NANOPARTICLES;

NANOPROBES;

ENZYME; NANOCLUSTER; NANOPARTICLE; QUANTUM DOT; REACTIVE OXYGEN METABOLITE; SILICA NANOPARTICLE; UNCLASSIFIED DRUG; UPCONVERSION NANOPARTICLE;

CAVEOLIN DEPENDENT ENDOCYTOSIS; CELL MEMBRANE; CELL NUCLEUS; CLATHRIN MEDIATED ENDOCYTOSIS; CYTOTOXICITY; ENDOCYTOSIS; FLUORESCENCE IMAGING; HUMAN; LYSOSOME; MITOCHONDRION; NANOPROBE; PARTICLE SIZE; PH; PHAGOCYTOSIS; PINOCYTOSIS; PRIORITY JOURNAL; REVIEW; SURFACE PROPERTY;

EID: 84901459213     PISSN: 01659936     EISSN: 18793142     Source Type: Journal    
DOI: 10.1016/j.trac.2014.03.003     Document Type: Review

References (68)

1. Barabási A.L., Oltvai Z.N. Network biology: understanding the cell's functional organization. Nat. Rev. Genet. 2004, 5:101-113.
2. Steck T.L. The organization of proteins in the human red blood cell membrane. A review. J. Cell. Biol. 1974, 62:1-19.
3. Mattick J.S., Mehler M.F. RNA editing, DNA recoding and the evolution of human cognition. Trends Neurosci. 2008, 31:227-233.
4. Valko M., Leibfritz D., Moncol J., Cronin M.T., Mazur M., Telser J. Free radicals and antioxidants in normal physiological functions and human disease. Int. J. Biochem. Cell Biol. 2007, 39:44-84.
5. Berry M.N., Friend D.S. High-yield preparation of isolated rat liver parenchymal cells: a biochemical and fine structural study. J. Cell Biol. 1969, 43:506-520.
6. 3-targeted magnetic resonance imaging. Nat. Med. 1998, 4:623-626.
7. Muhm J.R., Miller W.E., Fontana R.S., Sanderson D.R., Uhlenhopp M.A. Lung cancer detected during a screening program using four-month chest radiographs. Radiology 1983, 148:609-615.
8. Müller D.J., Dufrêne Y.F. Atomic force microscopy as a multifunctional molecular toolbox in nanobiotechnology. Nat. Nanotech. 2008, 3:261-269.
9. Yuste R. Fluorescence microscopy today. Nat. Methods 2005, 2:902-904.
10. Kobayashi H., Ogawa M., Alford R., Choyke P.L., Urano Y. New strategies for fluorescent probe design in medical diagnostic imaging. Chem. Rev. 2010, 110:2620-2640.
11. Tsien R.Y. The green fluorescent protein. Annu. Rev. Biochem. 1998, 67:509-544.
12. Han J., Burgess K. Fluorescent indicators for intracellular pH. Chem. Rev. 2009, 110:2709-2728.
13. Shaner N.C., Lin M.Z., McKeown M.R., Steinbach P.A., Hazelwood K.L., Davidson M.W., Tsien R.Y. Improving the photostability of bright monomeric orange and red fluorescent proteins. Nat. Methods 2008, 5:545-551.
14. Rumbut R.E., Sial A.J. Differential phototoxicity of fluorescent dye-labeled albumin conjugates. Microcirculation 1999, 6:205-213.
15. He X., Gao J., Gambhir S.S., Cheng Z. Near-infrared fluorescent nanoprobes for cancer molecular imaging: status and challenges. Trends Mol. Med. 2010, 16:574-583.
16. He X., Wang K., Cheng Z. In vivo near-infrared fluorescence imaging of cancer with nanoparticle-based probes. Wiley Interdiscip. Rev. Nanomed. Nanobiotechnol. 2010, 2:349-366.
17. Wang K., He X., Yang X., Shi H. Functionalized silica nanoparticles: a platform for fluorescence imaging at the cell and small animal levels. Acc. Chem. Res. 2013, 46:1367-1376.
18. Plumeré N., Ruff A., Speiser B., Feldmann V., Mayer H.A. Stöber silica particles as basis for redox modifications: particle shape, size, polydispersity, and porosity. J. Colloid Interface Sci. 2012, 368:208-219.
19. Wang L., Tan W. Multicolor FRET silica nanoparticles by single wavelength excitation. Nano Lett. 2006, 6:84-88.
20. He X., Wang Y., Wang K., Chen M., Chen S. Fluorescence resonance energy transfer mediated large stokes shifting near-infrared fluorescent silica nanoparticles for in vivo small-animal imaging. Anal Chem. 2012, 21:9056-9064.
21. Alivisatos A.P. Semiconductor clusters, nanocrystals, and quantum dots. Science 1996, 271:933-937.
22. Hu Y., Lindberg M., Koch S.W. Theory of optically excited intrinsic semiconductor quantum dots. Phys. Rev. B 1990, 42:e1713.
23. Han M., Gao X., Su J., Nie S. Quantum-dot-tagged microbeads for multiplexed optical coding of biomolecules. Nat. Biotechnol. 2001, 19:631-635.
24. Chan W.C.W., Nie S. Quantum dot bioconjugates for ultrasensitive nonisotopic detection. Science 1998, 281:2016-2018.
25. Lu Y., Chen W. Sub-nanometre sized metal clusters: from synthetic challenges to the unique property discoveries. Chem. Soc. Rev. 2012, 41:3594-3623.
26. Han B., Wang E. DNA-templated fluorescent silver nanoclusters. Anal. Bioanal. Chem. 2012, 402:129-138.
27. Yin J., He X., Wang K., Qing Z., Wu X., Shi H., Yang X. One-step engineering of silver nanoclusters-aptamer assemblies as luminescent labels to target tumor cells. Nanoscale 2012, 4:110-112.
28. Yin J., He X., Wang K., Xu F., Shangguan J., He D., Shi H. Label-free and turn-on aptamer strategy for cancer cells detection based on a DNA-silver nanocluster fluorescence upon recognition-induced hybridization. Anal. Chem. 2013, 85:12011-12019.
29. Wang F., Liu X. Recent advances in the chemistry of lanthanide-doped upconversion nanocrystals. Chem. Soc. Rev. 2009, 38:976-989.
30. Lin M., Zhao Y., Wang S., Liu M., Duan Z., Chen Y., Li F., Xu F., Lu T. Recent advances in synthesis and surface modification of lanthanide-doped upconversion nanoparticles for biomedical applications. Biotechnol. Adv. 2012, 30:1551-1561.
31. Yao C., Tong Y. Lanthanide ion-based luminescent nanomaterials for bioimaging. Trends Analyt. Chem. 2012, 39:60-71.
32. Liu Y., Tu D., Zhu H., Chen X. Lanthanide-doped luminescent nanoprobes: controlled synthesis, optical spectroscopy, and bioapplications. Chem. Soc. Rev. 2013, 42:6924-6958.
33. Zhu M., Nie G., Meng H., Xia T., Nel A., Zhao Y. Physicochemical properties determine nanomaterial cellular uptake, transport, and fate. Acc. Chem. Res. 2012, 46:622-631.
34. He C., Hu Y., Yin L., Tang C., Yin C. Effects of particle size and surface charge on cellular uptake and biodistribution of polymeric nanoparticles. Biomaterials 2010, 31:3657-3666.
35. He X., Liu F., Wang K., Ge J., Qin D., Gong P., Tan W. Bioeffects of different functionalized silica nanoparticles on HaCaT cell line. Chin. Sci. Bull. 2006, 51:1939-1946.
36. Xing X., He X., Peng J., Wang K., Tan W. Uptake of silica-coated nanoparticles by HeLa cells. J. Nanosci. Nanotechnol. 2005, 5:1688-1693.
37. Liu D., He X., Wang K., He C., Shi H., Jian L. Biocompatible silica nanoparticle-insulin conjugates for mesenchymal stem cell adipogenic differentiation. Bioconjug. Chem. 2010, 21:1673-1684.
38. Jin Y., Lohstreter S., Pierce D.T., Parisien J., Wu M., Hall C., Zhao J. Silica nanoparticles with continuously tunable sizes: synthesis and size effects on cellular contrast imaging. Chem. Mater. 2008, 20:4411-4419.
39. Varkouhi A.K., Scholte M., Storm G., Haisma H.J. Endosomal escape pathways for delivery of biologicals. J. Control. Release 2011, 151:220-228.
40. Huang X., Teng X., Chen D., Tang F., He J. The effect of the shape of mesoporous silica nanoparticles on cellular uptake and cell function. Biomaterials 2010, 31:438-448.
41. Buono C., Anzinger J.J., Amar M., Kruth H.S. Fluorescent pegylated nanoparticles demonstrate fluid-phase pinocytosis by macrophages in mouse atherosclerotic lesions. J. Clin. Invest. 2009, 119:e1373.
42. Jiang X., Röcker C., Hafner M., Brandholt S., Dörlich R.M., Nienhaus G.U. Endo- and exocytosis of zwitterionic quantum dot nanoparticles by live HeLa cells. ACS Nano 2010, 4:6787-6797.
43. Liu H., Wu S., Lu C., Yao M., Hsiao J.K., Hung Y., Lin Y., Mou C., Yang C., Huang D., Chen Y. Mesoporous silica nanoparticles improve magnetic labeling efficiency in human stem cells. Small 2008, 4:619-626.
44. Chen C., Ke J., Zhou X., Yi W., Brunzelle J.S., Li J., Yong E., Xu H., Melcher K. Structural basis for molecular recognition of folic acid by folate receptors. Nature 2013, 500:486-489.
45. Elnakat H., Ratman M. Distribution, functionality and gene regulation of folate receptor isoforms: implications in targeted therapy. Adv. Drug Deliv. Rev. 2004, 56:1067-1084.
46. Son M.J., Woolard K., Nam D.H., Lee J., Fine H.A. SSEA-1 is an enrichment marker for tumor-initiating cells in human glioblastoma. Cell Stem Cell 2009, 4:440-452.
47. Prutki M., Poljak-Blazi M., Jakopovic M., Tomas D., Stipancic I., Zarkovic N. Altered iron metabolism, transferrin receptor 1 and ferritin in patients with colon cancer. Cancer Lett. 2006, 238:188-196.
48. Estévez M.C., O'Donoghue M.B., Chen X., Tan W. Highly fluorescent dye-doped silica nanoparticles increase flow cytometry sensitivity for cancer cell monitoring. Nano Res. 2009, 2:448-461.
49. Berthiaume E.P., Medina C., Swanson J.A. Molecular size-fractionation during endocytosis in macrophages. J. Cell. Biol. 1995, 129:989-998.
50. Fehrenbacher N., Jaattela M. Lysosomes as targets for cancer therapy. Cancer Res. 2005, 65:2993-2995.
51. Hanaki K.I., Momo A., Oku T., Komoto A., Maenosono S., Yamaguchi Y., Yamamoto K. Semiconductor quantum dot/albumin complex is a long-life and highly photostable endosome marker. Biochem. Biophys. Res. Commun. 2003, 302:496-501.
52. Shi H., He X., Yuan Y., Wang K., Liu D. Nanoparticle-based biocompatible and long-life marker for lysosome labeling and tracking. Anal. Chem. 2010, 82:2213-2220.
53. Jean S.R., Tulumello D.V., Wisnovsky S.P., Lei E.K., Pereira M.P., Kelley S.O. Molecular vehicles for mitochondrial chemical biology and drug delivery. ACS Chem. Biol. 2014, 9:323-333.
54. Zhuang Q., Jia H., Du L., Li Y., Chen Z., Huang S., Liu Y. Targeted surface-functionalized gold nanoclusters for mitochondrial imaging. Biosens. Bioelectron. 2014, 55:76-82.
55. E. Ju, Z. Li, Z. Liu, J. Ren, X. Qu, Near-infrared light-triggered drug-delivery vehicle for mitochondria-targeted chemo-photothermal therapy, ACS Appl. Mater. Interfaces doi: 10.1021/am5000883.
56. Lamond A.I., Earnshaw W.C. Structure and function in the nucleus. Science 1998, 280:547-553.
57. Nigg E.A. Nucleocytoplasmic transport: signals, mechanisms and regulation. Nature 1997, 386:779-787.
58. Chen F., Gerion D. Fluorescent CdSe/ZnS nanocrystal-peptide conjugates for long-term, nontoxic imaging and nuclear targeting in living cells. Nano Lett. 2004, 4:1827-1832.
59. Fuller J.E., Zugates G.T., Ferreira L.S., Ow H.S., Nguyen N.N., Wiesner U.B., Langer R.S. Intracellular delivery of core-shell fluorescent silica nanoparticles. Biomaterials 2008, 29:1526-1532.
60. Liu J., Bu W., Pan L., Zhang S., Chen F., Zhou L., Zhao K., Peng W., Shi J. Simultaneous nuclear imaging and intranuclear drug delivery by nuclear-targeted multifunctional upconversion nanoprobes. Biomaterials 2012, 33:7282-7290.
61. Afjehi-Sadat L., Gruber-Olipitz M., Felizardo M., Slavc I., Lubec G. Expression of proteasomal proteins in ten different tumor cell lines. Amino Acids 2004, 27:129-140.
62. Malumbres M., Barbacid M. Cell cycle, CDKs and cancer: a changing paradigm. Nat. Rev. Cancer 2009, 9:153-166.
63. Chan C.F., Tsang M.K., Li H., Lan R., Chadbourne F.L., Chan W.L., Wong K.L. Bifunctional up-converting lanthanide nanoparticles for selective in vitro imaging and inhibition of cyclin D as anti-cancer agents. J. Mater. Chem. B 2014, 2:84-91.
64. Izumi H., Torigoe T., Ishiguchi H., Uramoto H., Yoshida Y., Tanabe M., Ise T., Murakami T., Yoshida T., Nomoto M., Kohno K. Cellular pH regulators: potentially promising molecular targets for cancer chemotherapy. Cancer Treat. Rev. 2003, 29:541-549.
65. Peng J., He X., Wang K., Tan W., Wang Y., Liu Y. Noninvasive monitoring of intracellular pH change induced by drug stimulation using silica nanoparticle sensors. Anal. Bioanal. Chem. 2007, 388:645-654.
66. Dennis A.M., Rhee W.J., Sotto D., Dublin S.N., Bao G. Quantum dot-fluorescent protein FRET probes for sensing intracellular pH. ACS Nano 2012, 6:2917-2924.
67. 2, a necessary evil for cell signaling. Science 2006, 312:1882-1883.
68. Oh W.K., Jeong Y.S., Kim S., Jang J. Fluorescent polymer nanoparticle for selective sensing of intracellular hydrogen peroxide. ACS Nano 2012, 6:8516-8524.