Coordinate control by vitamin A of keratin gene expression in human keratinocytes

• Published in: The Journal of biological chemistry Vol. 260; no. 26; pp. 14026 - 14029
• Main Authors: Gilfix, B M, Eckert, R L
• Format: Journal Article
• Language: English
• Published: Bethesda, MD Elsevier Inc 15.11.1985; American Society for Biochemistry and Molecular Biology
• Subjects: Analytical, structural and metabolic biochemistry; Benzoates - pharmacology; Biological and medical sciences; Cell Line; DNA; Epidermis - metabolism; Fetus; Fundamental and applied biological sciences. Psychology; Gene Expression Regulation - drug effects; Holoproteins; Humans; Keratins - genetics; Keratins - metabolism; Kinetics; Nucleic Acid Hybridization; Other proteins; Proteins; Retinoids; RNA, Messenger - metabolism; Trachea; Vitamin A - pharmacology; Human; Cell culture; Keratin; Regulation(control); Gene; Epidermis; Keratinocyte; Gene expression; Trachea; Retinol
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/S0021-9258(17)38679-9

In the present study, we examine the effects of vitamin A on keratin protein and mRNA levels in human keratinocytes. In epidermal keratinocytes, the levels of keratins 5, 6, 14, and 17 decrease and keratins 13 and 19 increase in response to increasing concentrations of a potent synthetic trans-retinoic acid analog, arotinoid Ro 13-6298. In tracheal keratinocytes, a similar suppression is observed for keratins 5, 6, 14, 17, and 18 and an increase in keratin 19. Both induction and suppression responses show identical kinetics and both processes are half-maximal at 5 nM arotinoid and maximal at 10 nM. Utilizing cDNAs specific for keratins 5, 6, 13, and 19, we demonstrate that the mRNA levels for these keratins change coordinately with the corresponding amount of keratin protein, indicating that the control of keratin protein expression most likely resides at the level of mRNA synthesis and/or degradation. The identical kinetics for all of the responses, both inductive and suppressive, suggests that a common mechanism controls the expression of these genes. These results indicate that vitamin A produces more sweeping changes in keratinocyte function than previously appreciated in that many and perhaps all keratins are modulated by vitamin A. Moreover, these responses are 10- to 100-fold less sensitive to retinoid than the process of envelope formation, suggesting that at least two sets of processes with different sensitivities to vitamin A are present in keratinocytes.