Formation and disintegration of cisternae of the endoplasmic reticulum visualized in live cells by conventional fluorescence and confocal laser scanning microscopy: Evidence for the involvement of calcium and the cytoskeleton

PROTOPLASMA ◽  
1990 ◽  
Vol 155 (1-3) ◽  
pp. 166-175 ◽  
Author(s):  
H. Quader
Keyword(s):  
Endoplasmic Reticulum ◽  
Confocal Laser Scanning Microscopy ◽  
Laser Scanning ◽  
Laser Scanning Microscopy ◽  
Confocal Laser Scanning ◽  
Scanning Microscopy ◽  
Live Cells ◽  
Confocal Laser

Visualization of the endoplasmic reticulum in living buds and branches of the moss Funaria hygrometrica by confocal laser scanning microscopy

Development ◽  
1990 ◽  
Vol 109 (4) ◽  
pp. 753-764
Author(s):  
M.M. McCauley ◽  
P.K. Hepler
Keyword(s):  
Endoplasmic Reticulum ◽  
Confocal Laser Scanning Microscopy ◽  
Laser Scanning ◽  
Side Branch ◽  
Laser Scanning Microscopy ◽  
Confocal Laser Scanning ◽  
Scanning Microscopy ◽  
Confocal Laser ◽  
Funaria Hygrometrica ◽  
Bud Formation

Caulonemata of the moss Funaria hygrometrica were vitally stained with the fluorescent, lipophilic carbocyanine dye DiOC6(3) and examined via confocal laser scanning microscopy. Although DiOC6(3) stained nearly all of the organelles, cortical endoplasmic reticulum (ER) could be resolved under favorable conditions and appeared as a network of irregular polygons, interspersed with lamellar cisternae in some cell types. The pattern of cortical ER was examined first during side initial formation and then in young branches and buds. The ER network extends into the outgrowth of a developing side initial, keeping pace with elongation of the outgrowth. Prior to the cell division that cuts off the outgrowth from the underlying cell, the network in the outgrowth becomes tighter, i.e. the polygons become smaller. If the side initial develops as a branch, this somewhat tighter ER network is maintained in the tip-growing side branch. If the side initial develops as a bud, dramatic changes in both the configuration and the quantity of the ER network occur. Coincident with the apical swelling that marks the first visible sign of bud formation, the network becomes increasingly tighter until eventually the polygonal configuration is barely discernible. The increased coverage of the bud cortex by the ER network demonstrates that a significant increase in the quantity of membranes also takes place during bud formation in Funaria.

Visualizing NO in live cells by confocal laser scanning microscopy

2012 ◽  
Vol 10 (s1) ◽  
pp. S11701-311703 ◽  
Author(s):  
Yimei Huang Yimei Huang ◽  
Hongqin Yang Hongqin Yang ◽  
Xiuqiu Shen Xiuqiu Shen ◽  
Yuhua Wang Yuhua Wang ◽  
Liqin Zheng Liqin Zheng ◽  
...  
Keyword(s):  
Confocal Laser Scanning Microscopy ◽  
Laser Scanning ◽  
Laser Scanning Microscopy ◽  
Confocal Laser Scanning ◽  
Scanning Microscopy ◽  
Live Cells ◽  
Confocal Laser

ACTIVATED SLUDGE FLOC CHARACTERIZATION BY CONFOCAL LASER SCANNING MICROSCOPY

2012 ◽  
Vol 11 (3) ◽  
pp. 669-674 ◽  
Author(s):  
Szabolcs Szilveszter ◽  
Botond Raduly ◽  
Szilard Bucs ◽  
Beata Abraham ◽  
Szabolcs Lanyi ◽  
...  
Keyword(s):  
Activated Sludge ◽  
Confocal Laser Scanning Microscopy ◽  
Laser Scanning ◽  
Laser Scanning Microscopy ◽  
Confocal Laser Scanning ◽  
Scanning Microscopy ◽  
Confocal Laser

scholarly journals Bacterial Colonization and Proliferation in Furcal Perforations Repaired by Different Materials: A Confocal Laser Scanning Microscopy Study

2021 ◽  
Vol 11 (8) ◽  
pp. 3403
Author(s):  
Shlomo Elbahary ◽  
Sohad Haj Yahya ◽  
Cemre Koç ◽  
Hagay Shemesh ◽  
Eyal Rosen ◽  
...  
Keyword(s):  
Confocal Laser Scanning Microscopy ◽  
Laser Scanning ◽  
Bacterial Colonization ◽  
Microscopy Study ◽  
Laser Scanning Microscopy ◽  
Confocal Laser Scanning ◽  
Scanning Microscopy ◽  
Confocal Laser ◽  
Repair Material ◽  
Dentinal Tubules

Following furcal perforation, bacteria may colonize the defect and cause inflammation and periodontal destruction. This study used confocal laser scanning microscopy (CLSM) to evaluate Enterococcus faecalis colonization and proliferation in furcal perforations repaired with different materials. Furcal perforations created in 55 extracted human mandibular molars were repaired using either MTA-Angelus, Endocem, or Biodentine and coronally subjected to E. faecalis suspension for 21 days. The specimens were then stained using a LIVE/DEAD Viability Kit and visualized by CLSM. The minimum and maximum depths of bacterial penetration into the dentinal tubules were 159 and 1790 μM, respectively, with a mean of 713 μM. There were significantly more live than dead bacteria inside the dentinal tubules (p = 0.0023) in all groups, and all three repair materials exhibited a similarly sized stained area (p = 0.083). However, there were significant differences in the numbers of dead bacteria at the circumference of the perforation defect (p = 0.0041), with a significantly higher ratio of live to dead bacteria in the MTA-Angelus group (p = 0.001). Following perforation repair, bacteria may colonize the interface between the repair material and dentin and may penetrate through the dentinal tubules. The type of repair material has a significant effect on the viability of the colonizing bacteria.

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