Confocal microscopy as a tool to reveal the tridimensional organization of intracellular lumens and intercellular cysts in a human colon adenocarcinoma cell line

ISSN:
0248-4900
Keywords:
adenocarcinoma cells ; confocal laser scanning microscopy ; intercellular cysts ; intracellular lumens
Source:
Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
Topics:
Biology
Type of Medium:
Electronic Resource
URL:
_version_ 1798291725558480896
autor Remy, L.
Gorvel, J.-P.
Jacquier, M.-F.
Rigal, A.
Davoust, J.
autorsonst Remy, L.
Gorvel, J.-P.
Jacquier, M.-F.
Rigal, A.
Davoust, J.
book_url http://dx.doi.org/10.1016/0248-4900(90)90339-5
datenlieferant nat_lic_papers
fussnote Adenocarcinoma cells often form intracellular lumens and intercellular cysts. In order to study the structural relationships between these lumens and the apical domain of normal enterocytes, we have applied electron microscopy and confocal microscopy to a cloned cell line derived from the human colon adenocarcinoma cell line LoVo which express a high number of intracellular lumens and intercellular cysts. Microvilli reminiscent of those detected in the brush border of small intestinal cells are formed in the two types of compartments. By immunofluorescence, we found that a 135 kDa membrane glycoprotein characterized by a monoclonal Ab and normally associated with the brush-border of enterocytes is expressed at the surface of the intracellular lumens and intercellular cysts present in the adenocarcinoma cells. Comparison of fluorescence and reflection contrast micrographs obtained by confocal microscopy demonstrate the presence of spherical intracellular lumens in the juxtanuclear region of single cells, and of more complex shaped intercellular cysts located within clusters of cells. The later cells form junctional complexes limiting an apical plasma membrane domain in contact with the intercellular cyst. It is suggested that the intracellular lumens may represent the abortive form of an apical plasma membrane due to the lack of components required to establish epithelial cell contacts. As opposed to conventional fluorescence microscopy, confocal microscopy allows rapid inspection of the tridimensional organization of intracellular lumens and intercellular cysts even when they are located in cell multilayers.
hauptsatz hsatz_simple
identnr NLZ18786893X
issn 0248-4900
journal_name Biology of the Cell
materialart 1
package_name Elsevier
publikationsort Amsterdam
publisher Elsevier
reference 69 (1990), S. 129-138
schlagwort adenocarcinoma cells
confocal laser scanning microscopy
intercellular cysts
intracellular lumens
search_space articles
shingle_author_1 Remy, L.
Gorvel, J.-P.
Jacquier, M.-F.
Rigal, A.
Davoust, J.
shingle_author_2 Remy, L.
Gorvel, J.-P.
Jacquier, M.-F.
Rigal, A.
Davoust, J.
shingle_author_3 Remy, L.
Gorvel, J.-P.
Jacquier, M.-F.
Rigal, A.
Davoust, J.
shingle_author_4 Remy, L.
Gorvel, J.-P.
Jacquier, M.-F.
Rigal, A.
Davoust, J.
shingle_catch_all_1 Remy, L.
Gorvel, J.-P.
Jacquier, M.-F.
Rigal, A.
Davoust, J.
Confocal microscopy as a tool to reveal the tridimensional organization of intracellular lumens and intercellular cysts in a human colon adenocarcinoma cell line
adenocarcinoma cells
confocal laser scanning microscopy
intercellular cysts
intracellular lumens
adenocarcinoma cells
confocal laser scanning microscopy
intercellular cysts
intracellular lumens
0248-4900
02484900
Elsevier
shingle_catch_all_2 Remy, L.
Gorvel, J.-P.
Jacquier, M.-F.
Rigal, A.
Davoust, J.
Confocal microscopy as a tool to reveal the tridimensional organization of intracellular lumens and intercellular cysts in a human colon adenocarcinoma cell line
adenocarcinoma cells
confocal laser scanning microscopy
intercellular cysts
intracellular lumens
adenocarcinoma cells
confocal laser scanning microscopy
intercellular cysts
intracellular lumens
0248-4900
02484900
Elsevier
shingle_catch_all_3 Remy, L.
Gorvel, J.-P.
Jacquier, M.-F.
Rigal, A.
Davoust, J.
Confocal microscopy as a tool to reveal the tridimensional organization of intracellular lumens and intercellular cysts in a human colon adenocarcinoma cell line
adenocarcinoma cells
confocal laser scanning microscopy
intercellular cysts
intracellular lumens
adenocarcinoma cells
confocal laser scanning microscopy
intercellular cysts
intracellular lumens
0248-4900
02484900
Elsevier
shingle_catch_all_4 Remy, L.
Gorvel, J.-P.
Jacquier, M.-F.
Rigal, A.
Davoust, J.
Confocal microscopy as a tool to reveal the tridimensional organization of intracellular lumens and intercellular cysts in a human colon adenocarcinoma cell line
adenocarcinoma cells
confocal laser scanning microscopy
intercellular cysts
intracellular lumens
adenocarcinoma cells
confocal laser scanning microscopy
intercellular cysts
intracellular lumens
0248-4900
02484900
Elsevier
shingle_title_1 Confocal microscopy as a tool to reveal the tridimensional organization of intracellular lumens and intercellular cysts in a human colon adenocarcinoma cell line
shingle_title_2 Confocal microscopy as a tool to reveal the tridimensional organization of intracellular lumens and intercellular cysts in a human colon adenocarcinoma cell line
shingle_title_3 Confocal microscopy as a tool to reveal the tridimensional organization of intracellular lumens and intercellular cysts in a human colon adenocarcinoma cell line
shingle_title_4 Confocal microscopy as a tool to reveal the tridimensional organization of intracellular lumens and intercellular cysts in a human colon adenocarcinoma cell line
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source_archive Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
timestamp 2024-05-06T08:37:11.898Z
titel Confocal microscopy as a tool to reveal the tridimensional organization of intracellular lumens and intercellular cysts in a human colon adenocarcinoma cell line
titel_suche Confocal microscopy as a tool to reveal the tridimensional organization of intracellular lumens and intercellular cysts in a human colon adenocarcinoma cell line
Adenocarcinoma cells often form intracellular lumens and intercellular cysts. In order to study the structural relationships between these lumens and the apical domain of normal enterocytes, we have applied electron microscopy and confocal microscopy to a cloned cell line derived from the human colon adenocarcinoma cell line LoVo which express a high number of intracellular lumens and intercellular cysts. Microvilli reminiscent of those detected in the brush border of small intestinal cells are formed in the two types of compartments. By immunofluorescence, we found that a 135 kDa membrane glycoprotein characterized by a monoclonal Ab and normally associated with the brush-border of enterocytes is expressed at the surface of the intracellular lumens and intercellular cysts present in the adenocarcinoma cells. Comparison of fluorescence and reflection contrast micrographs obtained by confocal microscopy demonstrate the presence of spherical intracellular lumens in the juxtanuclear region of single cells, and of more complex shaped intercellular cysts located within clusters of cells. The later cells form junctional complexes limiting an apical plasma membrane domain in contact with the intercellular cyst. It is suggested that the intracellular lumens may represent the abortive form of an apical plasma membrane due to the lack of components required to establish epithelial cell contacts. As opposed to conventional fluorescence microscopy, confocal microscopy allows rapid inspection of the tridimensional organization of intracellular lumens and intercellular cysts even when they are located in cell multilayers.
topic W
uid nat_lic_papers_NLZ18786893X