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L-proline is an essential amino acid for hepatocyte growth in culture.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 1984 Aug 16; Vol. 122 (3), pp. 884-91. - Publication Year :
- 1984
-
Abstract
- For improvement of the culture conditions of adult rat hepatocytes in primary culture in collagen coated dishes, effects of various commercial culture media on the induction of replicative DNA synthesis of the cells stimulated by insulin plus epidermal growth factor were studied. Proline-deficient media, such as Leibovitz's L-15, Eagle's minimal essential medium and Dulbecco's modified minimal essential medium, did not induce DNA synthesis in hepatocytes, whereas proline-rich media, such as Williams medium E, McCoy's 5A and Ham's F-12, induced markedly hepatocyte proliferation. Moreover, when the proline-deficient media were supplemented with L-proline, the cells synthesized DNA in response to the two hormones. Cis-4-hydroxyl-L-proline strongly inhibited the induction of DNA synthesis, without affecting protein synthesis of the cells or showing any cytotoxicity. This inhibition was recovered completely by adding excess proline to the medium. Addition of other amino acids not present in the medium did not promote DNA synthesis. These findings indicate that L-proline is essential for induction of hepatocyte proliferation in culture, through its affect on synthesis of intracellular collagen.
- Subjects :
- Animals
Cell Division drug effects
Cells, Cultured
Culture Media
DNA Replication
Epidermal Growth Factor pharmacology
Hydroxyproline pharmacology
Insulin pharmacology
Kinetics
Liver drug effects
Liver metabolism
Male
Proline metabolism
Rats
Rats, Inbred Strains
Liver cytology
Proline pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0006-291X
- Volume :
- 122
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 6383376
- Full Text :
- https://doi.org/10.1016/0006-291x(84)91173-2