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The smooth muscle cell. III. Elastin synthesis in arterial smooth muscle cell culture

Primate arterial smooth muscle cells and skin fibroblasts were examined for their ability to synthesize elastin in culture. In the presence of the lathyrogen beta-aminopropionitrile, the smooth muscle cells incorporate [3H]lysine into a lysyl oxidase substrate that was present in the medium and asso...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1976
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2109664/
https://www.ncbi.nlm.nih.gov/pubmed/1030702
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description Primate arterial smooth muscle cells and skin fibroblasts were examined for their ability to synthesize elastin in culture. In the presence of the lathyrogen beta-aminopropionitrile, the smooth muscle cells incorporate [3H]lysine into a lysyl oxidase substrate that was present in the medium and associated with the cell layer. A component having a mol wt of 72,000 and an electrophoretic mobility similar to that of authentic tropoelastin was isolated from the labeled smooth muscle cells by coacervation and fractionation with organic solvents. In the absence of beta-aminopropionitrile, long-term cultures of smooth muscle cells incorporated [14C]lysine into desmosine and isodesmosine, the cross-link amino acids unique to elastin. In contrast, no desmosine formation occurred in the fibroblast cultures. These characteristics demonstrate that arterial smooth muscle cells are capable of synthesizing both soluble and cross-lined elastin in culture.
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spelling pubmed-21096642008-05-01 The smooth muscle cell. III. Elastin synthesis in arterial smooth muscle cell culture J Cell Biol Articles Primate arterial smooth muscle cells and skin fibroblasts were examined for their ability to synthesize elastin in culture. In the presence of the lathyrogen beta-aminopropionitrile, the smooth muscle cells incorporate [3H]lysine into a lysyl oxidase substrate that was present in the medium and associated with the cell layer. A component having a mol wt of 72,000 and an electrophoretic mobility similar to that of authentic tropoelastin was isolated from the labeled smooth muscle cells by coacervation and fractionation with organic solvents. In the absence of beta-aminopropionitrile, long-term cultures of smooth muscle cells incorporated [14C]lysine into desmosine and isodesmosine, the cross-link amino acids unique to elastin. In contrast, no desmosine formation occurred in the fibroblast cultures. These characteristics demonstrate that arterial smooth muscle cells are capable of synthesizing both soluble and cross-lined elastin in culture. The Rockefeller University Press 1976-03-01 /pmc/articles/PMC2109664/ /pubmed/1030702 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
The smooth muscle cell. III. Elastin synthesis in arterial smooth muscle cell culture
title The smooth muscle cell. III. Elastin synthesis in arterial smooth muscle cell culture
title_full The smooth muscle cell. III. Elastin synthesis in arterial smooth muscle cell culture
title_fullStr The smooth muscle cell. III. Elastin synthesis in arterial smooth muscle cell culture
title_full_unstemmed The smooth muscle cell. III. Elastin synthesis in arterial smooth muscle cell culture
title_short The smooth muscle cell. III. Elastin synthesis in arterial smooth muscle cell culture
title_sort smooth muscle cell. iii. elastin synthesis in arterial smooth muscle cell culture
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2109664/
https://www.ncbi.nlm.nih.gov/pubmed/1030702