Open AccessCytofluorometry and fluorescence confocal laser scanning microscopy (CLSM) in the study of neutral lipid dynamics in Paramecium primaurelia mating types during cell line development
Author(s) -
Ramoino Paola,
Diaspro Alberto,
Fato Marco,
Beltrame Francesco
Publication year - 1999
Publication title -
cytometry
Language(s) - English
Resource type - Journals
eISSN - 1097-0320
pISSN - 0196-4763
DOI - 10.1002/(sici)1097-0320(19990401)35:4<346::aid-cyto7>3.0.co;2-p
Subject(s) - biology , nile red , mating type , mating , lipid droplet , confocal laser scanning microscopy , confocal microscopy , fluorescence microscope , microbiology and biotechnology , flow cytometry , cell type , biophysics , cell culture , fluorescence , cell , biochemistry , zoology , genetics , gene , physics , quantum mechanics
Background: In Paramecium primaurelia , an exconjugant cell can produce two lines with different mating capacities. Mating type II cells can form a higher food vacuole number and digest the nutrient taken up in a shorter time; thus, mating type II cells grow at a faster rate than do mating type I cells. The present study was done to determine whether cells that ingest more nutrients also have a larger amount of storage lipids. Methods: Quantitative and qualitative determinations of neutral lipids were obtained by means of cytofluorometry and fluorescence confocal laser scanning microscopy (CLSM), respectively, by using nile red on cells in different physiologic states. Results: Lipid droplet number and neutral lipid content were higher in mating type II cells than in mating type I cells in the early logarithmic growth phase (i.e., immature well‐fed cells). These values were reversed during the middle and the late logarithmic phases and became equal in the stationary phase (i.e., mature starved cells). In well‐fed cells maintained with food excess, differences in neutral lipid content between the two mating types also were present in mature cells. Conclusions: Although differences between mating type I and mating type II lines were not correlated to cell size, a relation was found between lipid content and food ingestion capacity. A depletion of bacteria in the culture medium could be responsible for the lack of differences in mature starved cells. CLSM allowed us to gather volume information about the lipid droplet distribution within the cell. Cytometry 35:346–352, 1999. © 1999 Wiley‐Liss, Inc.