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Xenopus laevis and its oocyte

Laser-Scanning Microscopy as a Tool to Study the Spatio-Temporal Organization of InsP 3 -Mediated Ca 2+ signaling. Xenopus laevis and its oocyte. IP 3 /Ca 2+ signaling pathway in the oocyte.

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Xenopus laevis and its oocyte

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  1. Laser-Scanning Microscopy as a Tool to Study the Spatio-Temporal Organization of InsP3-Mediated Ca 2+ signaling

  2. Xenopus laevis and its oocyte

  3. IP3/Ca2+ signaling pathway in the oocyte

  4. Video-rate confocal microscopy in conjunction with UV photolysis of caged-IP3 and Ca2+sensitive dyes reveals a high degree of spatio-temporal organization of Ca2+release in the oocyte

  5. Optical Schematic of Confocal Line-Scan Microscope (CLSM)

  6. Comparative resolution of the system

  7. Optical Schematic and comparative resolution of the Video-Rate CLSM

  8. Do elementary events arise from the activity of a single IP3R?

  9. Line-scan images of elementary events evoked by the photorelease of InsP3

  10. The spread of Ca2+ during elementary events is consistent with passive diffusion from a point source

  11. Does CICR and Ca2+ diffusion between sites give rise to global waves?

  12. Clustering of release sites gives rise to salutatory wave propagation

  13. EGTA spatially decouples individual release sites to block wave propagation

  14. What is the radial organization of release sites?

  15. Optical schematic of the piezo z-scan unit and representative images of Ca2+ release events in the z-axis

  16. Rapid localized Ca2+ transients as resolved with real-time x-z scanning confocal microscopy

  17. Model of InsP3-mediated Ca2+ release in the oocyte

  18. Practical theory of 2-photon microscopy 1. Near simultaneous absorption of the energy of two infrared photons results in excitation of a fluorochrome that would normally be excited by a single photon of twice the energy. 2. The probability of excitation depends on the square of the infrared intensity and decreases as the inverse 4th power of the distance from the focus volume.

  19. Advantages of 2-Photon microscopy 1. Increased penetration of infrared light allows deeper imaging. 2. No out-of-focus fluorescence, thus increased signal to noise. 3. Photo-damage and bleaching are confined to diffraction limited spot. 4. Multiple fluorochrome excitation allows simultaneous, diffraction limited, co-localization. 5. Imaging of UV-excited compounds with conventional optics.

  20. Optical schematic of video-rate 2-photon line-scan microscope 3-D pollen grain

  21. 2-photon imaging of pyramidal cells in acute cortical slices

  22. 2-Photon Ca 2+ imaging in cortical slices following antidromic stimulation

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