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PMID: 4169965 Published · ppublish English Journal Article

The response of cultured mammalian cells to diphtheria toxin. II. The resistant cell: enhancement of toxin action by poly-L-ornithine.

The Journal of experimental medicine ·Vol. 127 ·No. 3 ·1968-03-01 ·Pages 541-54

Moehring JM, Moehring TJ

Abstract

We have investigated the response of the resistant mouse L cell to diphtheria toxin. Intact cells and cell-free systems were studied. It was determined that the cell-free system is as sensitive to toxin as those from sensitive reticulocyte, HeLa, and KB cells previously studied. Poly-L-ornithine, reported to stimulate macromolecular uptake, enhanced toxin activity under conditions which also stimulated acid phosphatase activity. Resistance, in the L cell, appears to be linked to the cell membrane and the process of macromolecular uptake, and not to any intrinsic property of either the polyribosomes or associated protein synthesizing factors. Because of the unique way in which diphtheria toxin inhibits protein synthesis, the ability of poly-L-ornthine to enhance this action provides convincing evidence that poly-L-ornithine stimulates a true absorption of macromolecules and not just increased surface adsorption.

MeSH Terms
Acid Phosphatase Amino Acids/metabolism Animals Carbon Isotopes Cell-Free System Culture Media Diphtheria Toxin/pharmacology HeLa Cells Histocytochemistry In Vitro Techniques L Cells Mice Microscopy, Phase-Contrast Ornithine/pharmacology Puromycin/pharmacology Ribonucleases/pharmacology Ribosomes/metabolism Staining and Labeling Valine/metabolism
Chemicals
Amino Acids Carbon Isotopes Culture Media Diphtheria Toxin Puromycin Ornithine Ribonucleases Acid Phosphatase Valine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Moehring J M
Moehring T J
References (8)
8 references, click to expand
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1968-03-01
Pages
541-54
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2138456
Subset
IM
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