Functional imaging of living Paramecium by means of confocal and two-photon excitation fluorescence microscopy

Alberto Diaspro, Paola Fronte, Marco Raimondo, Marco Fato, Gianluca DeLeo, Francesco Beltrame, Fabio Cannone, Giberto Chirico, Paola Ramoino

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

Confocal and Two-photon excitation laser scanning microscopy allow gathering three-dimensional and temporal information from biological systems exploiting fluorescence labeling and autofluorescence properties. In this work we study biological events linked to functionality in Paramecium primaurelia. The internalization of material in ciliated one-celled organisms (protozoa) occurs via different mechanisms, even if most of nutrients, particulate or not, is taken up by food vacuoles formed at the bottom of the oral cavity. The endocytosis of small-sized molecules occurs at the parasomal sacs, located next the ciliar basal bodies. Vital fluorescent dyes (BSA-FITC, WGA-FITC, dextran-Texas Red, cholesteryl-Bodipy) and autofluorescence were used to study formation, movement, and fusion of vesicles during endocytosis and phagocytosis of Paramecium primaurelia. By immobilizing living cells pulsed with food vacuole and endosome markers at successive times after chasing in unlabeled medium, the intracellular movement and fusion of food vacuoles and of endosomes were visualized. A temporal analysis of fluorescence images and the false-color technique were used. Starting from time series or 3D data sets composite images were generated by associating with each originally acquired image a different color corresponding to each sampling point in time and along the z-axis. Second Harmonic Generation Imaging attempts are also outlined.

Original languageEnglish (US)
Pages (from-to)24-31
Number of pages8
JournalProceedings of SPIE - The International Society for Optical Engineering
Volume4622
Issue number1
DOIs
StatePublished - May 28 2002

Fingerprint

paramecia
Fluorescence Microscopy
Vacuole
Confocal
Fluorescence microscopy
food
Autofluorescence
Photon
Photons
Excitation
Imaging
microscopy
Imaging techniques
fluorescence
Fluorescence
Fusion
photons
Fusion reactions
protozoa
fusion

Keywords

  • Confocal Microscopy
  • Fluorescence functional imaging
  • Paramecium primaurelia
  • Second-Harmonic Generation Imaging
  • Three-dimensional imaging
  • Two-photon excitation microscopy

ASJC Scopus subject areas

  • Electronic, Optical and Magnetic Materials
  • Condensed Matter Physics
  • Computer Science Applications
  • Applied Mathematics
  • Electrical and Electronic Engineering

Cite this

Functional imaging of living Paramecium by means of confocal and two-photon excitation fluorescence microscopy. / Diaspro, Alberto; Fronte, Paola; Raimondo, Marco; Fato, Marco; DeLeo, Gianluca; Beltrame, Francesco; Cannone, Fabio; Chirico, Giberto; Ramoino, Paola.

In: Proceedings of SPIE - The International Society for Optical Engineering, Vol. 4622, No. 1, 28.05.2002, p. 24-31.

Research output: Contribution to journalArticle

Diaspro, Alberto ; Fronte, Paola ; Raimondo, Marco ; Fato, Marco ; DeLeo, Gianluca ; Beltrame, Francesco ; Cannone, Fabio ; Chirico, Giberto ; Ramoino, Paola. / Functional imaging of living Paramecium by means of confocal and two-photon excitation fluorescence microscopy. In: Proceedings of SPIE - The International Society for Optical Engineering. 2002 ; Vol. 4622, No. 1. pp. 24-31.
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