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[FP-SA-43] Ocular Imaging
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Apr 05 (Sat)
15:30 - 17:00
Room 13 - Tokyo International Forum 4F G402
Ocular Imaging
Chair)Yoko Miura、Chair)Dirk-Uwe Bartsch


Duration 5min, Q&A 3min

Watching Dying RGC-5 Cells by Using Raman Microscopy

Takeshi Morimoto
Takeshi Morimoto Hiroyuki Kanda Katsumasa Fujita Kohji Nishida Takashi Fujikado

Label-free imaging is desirable for elucidating morphological and biochemical changes of neurons in vitro and in vivo. Raman microscopy provides high chemical contrast without requiring preprocessing or fluorescence staining of samples. In the present study¸ we demonstrated dynamic imaging of molecular distribution in unstained RGC-5 cells during the glutamine-induced death process using Raman microscopy.

Immortalized retinal ganglion cells (RGC-5) were used as a sample in all experiments.

Our originally developed slit-scanning Raman microscopy was used in this study. All the hyperspectral Raman scattering images were obtained with 532 nm excitation from a frequency-doubled NdYVO4 laser.
Prior to Raman imaging¸ the cells were seeded on a crystal and cultured. For Raman imaging¸ the culture was maintained in a Hepes-buffered Tyrode´s solution and then was exposed to 400 mM glutamate. Raman scattering images were taken before and after administration of glutamate at 0¸30¸60¸120 minutes. The distribution of cytochrome c was reconstructed from the intensity distribution of the Raman peak at 753cm¯¹ at each time points.Other cultures were also stained with Mitotracker or anti-cytochrome c antibody to compare the Raman images of cytochrome c.

Results and Conclusion
we imaged the dynamic molecular distributions of cytochrome c in unstained RGC-5 cells. After the administration of glutamate, the intensity of cytochrome c Raman peak decreased¸ and the Raman signal distribution was seen to diffuse into the cell body and the nuclear. Raman images resembled the image of immunostaining of Mitotracker and cytochrome c.
 We revealed time-resolved distributions of cytochrome c in RGC-5 cells in the process of glutamate-induced cell death without the need for fluorescent labels or markers. Raman microscopy enabled dynamic imaging of molecular distributions in living cells with high temporal and spatial resolution.

[ Keyword ]
Cell death / Raman microscopy / Retinal ganglion cell

[ Conflict of Interest ]

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