Erratum: Label-free characterization of emerging human neuronal networks (Scientific Reports (2015) 4 (4434) DOI: 10.1038/srep04434);Label-Free Characterization of Emerging Human Neuronal Networks

Scientific Reports

Volumn 4, Issue , 2014, Pages

  Mir, Mustafa ^a,d   Kim, Taewoo ^a   Majumder, Anirban ^b   Xiang, Mike ^a   Wang, Ru ^a   Liu, S Chris ^c   Gillette, Martha U ^c   Stice, Steven ^b   Popescu, Gabriel ^a  

^a University of Illinois at Urbana Champaign   (United States)

^b UNIVERSITY OF GEORGIA   (United States)

^c UNIVERSITY OF ILLINOIS AT URBANA CHAMPAIGN   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

LITHIUM CHLORIDE;

ARTICLE; BIOLOGICAL MODEL; CELL CULTURE; CELL DIFFERENTIATION; CYTOLOGY; EQUIPMENT; GROWTH, DEVELOPMENT AND AGING; HUMAN; INTERFEROMETRY; METHODOLOGY; NERVE CELL; NERVE CELL NETWORK; PHYSIOLOGY; STEM CELL; TRANSPORT AT THE CELLULAR LEVEL;

BIOLOGICAL TRANSPORT; CELL DIFFERENTIATION; CELLS, CULTURED; HUMANS; INTERFEROMETRY; LITHIUM CHLORIDE; MODELS, NEUROLOGICAL; NERVE NET; NEURONS; STEM CELLS;

EID: 84906897828     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep11311     Document Type: Erratum

References (51)

1. Millet, L. J. & Gillette, M. U. New perspectives on neuronal development via microfluidic environments. Trends Neurosci. 35, 752-761 (2012).
2. Kerr, J. N. D. et al. Spatial organization of neuronal population responses in layer 2/3 of rat barrel cortex. J. Neurosci. 27, 13316-13328 (2007).
3. Grinvald, A., Lieke, E., Frostig, R. D., Gilbert, C. D. & Wiesel, T. N. Functional Architecture of Cortex Revealed by Optical Imaging of Intrinsic Signals. Nature 324, 361-364 (1986).
4. Sato, T. R., Gray, N. W., Mainen, Z. F. & Svoboda, K. The functional microarchitecture of the mouse barrel cortex. PLoS. Biol. 5, 1440-1452 (2007).
5. Millet, L. J., Bora, A., Sweedler, J. V. & Gillette, M. U. Direct cellular peptidomics of supraoptic magnocellular and hippocampal neurons in low-density co-cultures. ACS Chem. Neurosci. 1, 36-48 (2010).
6. Esch, T., Lemmon, V. & Banker, G. Local presentation of substrate molecules directs axon specification by cultured hippocampal neurons. J. Neurosci. 19, 6417-6426 (1999).
7. Fozdar, D. Y., Lee, J. Y., Schmidt, C. E. & Chen, S. C. Selective axonal growth of embryonic hippocampal neurons according to topographic features of various sizes and shapes. Int. J. Nanomed. 6, 45-57 (2011).
8. Hatton, G. I. Dynamic neuronal-glial interactions: an overview 20 years later. Peptides 25, 403-411 (2004).
9. Kerlin, A. M., Andermann, M. L., Berezovskii, V. K. & Reid, R. C. Broadly tuned response properties of diverse inhibitory neuron subtypes in mouse visual cortex. Neuron 67, 858-871 (2010).
10. Kim, H. J. et al. Integrated microfluidics platforms for investigating injury and regeneration of CNS axons. Ann. Biomed. Eng. 40, 1268-1276 (2012).
11. Kleinfeld, D., Kahler, K. H. & Hockberger, P. E. Controlled Outgrowth of Dissociated Neurons on Patterned Substrates. J. Neurosci. 8, 4098-4120 (1988).
12. Majumdar, D., Gao, Y. D., Li, D. Y. & Webb, D. J. Co-culture of neurons and glia in a novel microfluidic platform. J. Neurosci. Meth. 196, 38-44 (2011).
13. Nedelec, S. et al. Concentration-dependent requirement for local protein synthesis in motor neuron subtype-specific response to axon guidance cues. J. Neurosci. 32, 1496-1506 (2012).
14. Gobel, W. & Helmchen, F. In vivo calcium Imaging of neural network function. Physiology 22, 358-365 (2007).
15. Banker, G. A. & Cowan, W. M. Further Observations on Hippocampal-Neurons in Dispersed Cell-Culture. J. Comp. Neurol. 187, 469-493 (1979).
16. Valtorta, F., Pennuto, M., Bonanomi, D. & Benfenati, F. Synaptophysin: leading actor or walk-on role in synaptic vesicle exocytosis? Bioessays 26, 445-453 (2004).
17. Lundby, A., Mutoh, H., Dimitrov, D., Akemann, W. & Knopfel, T. Engineering of a Genetically Encodable Fluorescent Voltage Sensor Exploiting Fast Ci-VSP Voltage-Sensing Movements. PLoS One 3, e2514 (2008).
18. Miller, E. W. et al. Optically monitoring voltage in neurons by photo-induced electron transfer through molecular wires. Proc. Natl. Acad. Sci. USA 109, 2114-2119 (2012).
19. Erickson, J., Tooker, A., Tai, Y. C. & Pine, J. Caged neuron MEA: A system for long-term investigation of cultured neural network connectivity. J. Neurosci. Meth. 175, 1-16 (2008).
20. Gross, G. W., Rieske, E., Kreutzberg, G. W. & Meyer, A. A new fixed-array multi-microelectrode system designed for long-term monitoring of extracellular single unit neuronal activity in vitro. Neurosci. Lett. 6, 101-105 (1977).
21. Hardelauf, H. et al. High fidelity neuronal networks formed by plasma masking with a bilayer membrane: analysis of neurodegenerative and neuroprotective processes. Lab Chip 11, 2763-2771 (2011).
22. Thery, M. Micropatterning as a tool to decipher cellmorphogenesis and functions. J. Cell. Sci. 123, 4201-4213 (2010).
23. Nelson, C. M. & Tien, J. Microstructured extracellular matrices in tissue engineering and development. Curr. Opin. Biotech. 17, 518-523 (2006).
24. Yang, I. H., Siddique, R., Hosmane, S., Thakor, N. & Hoke, A. Compartmentalized microfluidic culture platform to study mechanism of paclitaxel-induced axonal degeneration. Exp. Neurol. 218, 124-128 (2009).
25. von Philipsborn, A. C., Lang, S., Jiang, Z., Bonhoeffer, F. & Bastmeyer, M. Substrate-bound protein gradients for cell culture fabricated by microfluidic networks and microcontact printing. Sci. STKE 2007, pl6 (2007).
26. Wang, J. Y. et al. Microfluidics: A new cosset for neurobiology. Lab Chip 9, 644-652 (2009).
27. Kunze, A., Meissner, R., Brando, S. & Renaud, P. Co-Pathological Connected Primary Neurons in a Microfluidic Device for Alzheimer Studies. Biotechnol. Bioeng. 108, 2241-2245 (2011).
28. Millet, L. J., Collens, M. B., Perry, G. L. & Bashir, R. Pattern analysis and spatial distribution of neurons in culture. Integr. Biol. (Camb) 3, 1167-1178 (2011).
29. Wang, Z. et al. Spatial light interference microscopy (SLIM). Opt Express 19, 1016-1026 (2011).
30. Wang, Z. & Popescu, G. Quantitative phase imaging with broadband fields. Appl. Phys. Lett. 96, 051117 (2010).
31. Popescu, G. Quantitative phase imaging of cells and tissues. (McGraw-Hill, New York, 2011).
32. Mir, M., Bhaduri, B., Wang, R., Zhu, R. & Popescu, G. Chapter 3-Quantitative Phase Imaging. Progress in Optics, Wolf, E. (ed.) 133-217 (Elsevier, Oxford, 2012).
33. Barer, R. Interference microscopy and mass determination. Nature 169, 366-367 (1952).
34. Popescu, G. et al. Optical imaging of cell mass and growth dynamics. Am. J. Physiol. Cell. Physiol. 295, C538-C544 (2008).
35. Mir, M. et al. Optical measurement of cycle-dependent cell growth. Proc. Natl. Acad. Sci. USA 108, 13124-13129 (2011).
36. Wang, R. et al. One-dimensional deterministic transport in neurons measured by dispersion-relation phase spectroscopy. J. Phys-Condens. Mat. 23, 374107 (2011).
37. Wang, R. et al. Dispersion-relation phase spectroscopy of intracellular transport. Opt. Exp. 19, 20571-20579 (2011).
38. Ding, H., Wang, Z., Nguyen, F., Boppart, S. A. & Popescu, G. Fourier Transform Light Scattering of Inhomogeneous and Dynamic Structures. Phys. Rev. Lett. 101, 238102 (2008).
39. Ding, H. F., Nguyen, F., Boppart, S. A. & Popescu, G. Optical properties of tissues quantified by Fourier-transform light scattering. Opt. Lett. 34, 1372-1374 (2009).
40. Ding, H. F., Millet, L. J., Gillette, M. U. & Popescu, G. Actin-driven cell dynamics probed by Fourier transform light scattering. Biomed. Opt. Exp. 1, 260-267 (2010).
41. Lim, J. et al. Born approximation model for light scattering by red blood cells. Biomed. Opt. Exp. 2, 2784-2791 (2011).
42. Hunter, M. et al. Tissue self-affinity and polarized light scattering in the born approximation: a new model for precancer detection. Phys. Rev. Lett. 97, 138102 (2006).
43. Dhara, S. K. et al. Genetic Manipulation of Neural Progenitors Derived from Human Embryonic Stem Cells. Tissue. Eng. Pt. A 15, 3621-3634 (2009).
44. Dhara, S. K. et al. Human neural progenitor cells derived from embryonic stem cells in feeder-free cultures. Differentiation 76, 454-464 (2008).
45. Jin, K. L. et al. Transplantation of human neural precursor cells in Matrigel scaffolding improves outcome from focal cerebral ischemia after delayed postischemic treatment in rats. J. Cereb. Blood Flow Metab. 30, 534-544 (2010).
46. Majumder, A. et al. Neurotrophic Effects of Leukemia Inhibitory Factor on Neural Cells Derived from Human Embryonic Stem Cells. Stem Cells 30, 2387-2399 (2012).
47. Young, A. et al. Ion channels and ionotropic receptors in human embryonic stem cell derived neural progenitors. Neuroscience 192, 793-805 (2011).
48. Harrill, J. A., Freudenrich, T. M., Robinette, B. L. & Mundy, W. R. Comparative sensitivity of human and rat neural cultures to chemical-induced inhibition of neurite outgrowth. Toxicol. Appl. Pharm. 256, 268-280 (2011).
49. Mackintosh, F. C. & Schmidt, C. F. Active cellular materials. Curr. Opin. Cell. Biol. 22, 29-35 (2010).
50. Brangwynne, C. P., Koenderink, G. H., MacKintosh, F. C. & Weitz, D. A. Intracellular transport by active diffusion. Trends. Cell. Biol. 19, 423-427 (2009).
51. Barer, R. Determination of dry mass, thickness, solid and water concentration in living cells. Nature 172, 1097-1098 (1953).