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PMID: 13664683 Published · ppublish English Journal Article

The relation between protein synthesis and lipide accumulation in L strain cells and Ehrlich ascites cells.

The Journal of biophysical and biochemical cytology ·Vol. 5 ·No. 3 ·1959-05-25 ·Pages 421-31

KING DW, SOCOLOW EL, BENSCH KG

Abstract

It has long been known that fat accumulates in old injured cells both in tissue culture and in many mammalian disease states. The use of L cells grown in suspension tissue culture permitted the opportunity to study conditions in which lipide accumulation could be retarded or accelerated. These cultures exhibit a three-phase growth curve which is similar to that previously found with bacteria and consists of a lag period, logarithmic growth period, and stationary period. Daily aliquots were removed from cultures going through these phases and protein and cholesterol content correlated with cell division. It was found that L cells gradually accumulated lipide in the cell concurrent with retardation of cell division and protein synthesis. Conversely old lipide-laden cells, placed in fresh media and encouraged to active division with net protein synthesis progressed from a high to a low lipide/cell ratio over a period of 2 to 4 days. An amino acid analogue p-fluorophenylalanine and a mitotic inhibitor, colchicine, also markedly increased the lipide/cell ratio. Similar results were found in in vitro experiments with Ehrlich ascites cells.

Keywords
LIPIDS/metabolism NEOPLASMS/metabolism PROTEINS/metabolism
MeSH Terms
Animals Ascites Cell Division Cholesterol L Cells Lipid Metabolism Mice Neoplasms/metabolism Protein Biosynthesis Proteins/metabolism
Chemicals
Proteins Cholesterol
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
KING D W
SOCOLOW E L
BENSCH K G
References (22)
22 references, click to expand
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Article Info
Journal
The Journal of biophysical and biochemical cytology
Abbr.
J Biophys Biochem Cytol
ISSN
0095-9901
Published
1959-05-25
Pages
421-31
Language
English
Region
United States
NLM ID
17840020R
PMCID
PMC2224672
Subset
OM
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