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PMID: 3383243 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Dynamic behavior of endoplasmic reticulum in living cells.

Cell ·Vol. 54 ·No. 1 ·1988-07-01 ·Pages 37-46

Lee C, Chen LB

Abstract

Endoplasmic reticulum (ER) was studied by fluorescence microscopy of living CV-1 cells treated with the fluorescent carbocyanine dye DiOC6(3). Using video recording and image processing techniques, several distinct forms of highly localized movements of ER were documented, categorized, and analyzed in terms of mechanism and structural implications. These include tubule branching, ring closure, and sliding. These localized movements have been observed to generate the basic elements of ER: linear tubules, polygonal reticulum, and triple junctions. We propose that as such they act as the mechanism for constructing the polygonal lattice of interconnected membrane tubules that constitutes ER. The nature of these movements suggests possible involvement of the cytoskeleton, and, in view of the close correlations in the distributions of ER and microtubules, and the accompanying paper (Dabora and Sheetz), it is possible that microtubules may play a role in generating ER motility and in constructing and maintaining the ER network in living cells.

MeSH Terms
Animals Carbocyanines Cell Line Endoplasmic Reticulum/physiology,ultrastructure Fluorescent Dyes Image Processing, Computer-Assisted Intercellular Junctions/physiology,ultrastructure Microscopy, Fluorescence Microtubules/physiology,ultrastructure Videotape Recording
Chemicals
Carbocyanines Fluorescent Dyes 3,3'-dihexyl-2,2'-oxacarbocyanine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Lee C
Dana-Farber Cancer Institute, Boston, Massachusetts 02115.
Chen L B
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1988-07-01
Pages
37-46
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NCI NIH HHS · CA19589 · United States
NCI NIH HHS · CA22427 · United States
NIGMS NIH HHS · GM38318 · United States
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