Abstract
Persistent infections of C6 rat astrocytoma cells with measles (subacute sclerosing panencephalitis [SSPE]) virus (C6/SSPE cells) or canine distemper virus (C6/CDV cells) cause a loss of endothelin-1 (ET-1) binding to its specific receptors (ETRA type) and subsequent ET-1-induced Ca2+ signaling. It was the aim of this study to investigate the underlying mechanism of this phenomenon in more detail. By using an RNase protection assay, it was found that ETRA mRNA disappears, whereas other cellular mRNA species, e.g., beta-actin mRNA, were not influenced. The data show that the loss of the ET-1 signaling pathway in C6/SSPE and C6/CDV cells is due to a receptor downregulation at the transcriptional level.
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- Andersson J., Ehrnst A., Larsson P. H., Hedlund K. O., Norrby E., Nybom R., Forsgren M., Olding-Stenquist E., Persson B. Visualization of defective measles virus particles in cerebrospinal fluid in subacute sclerosing panencephalitis. J Infect Dis. 1987 Dec;156(6):928–933. doi: 10.1093/infdis/156.6.928. [DOI] [PubMed] [Google Scholar]
- Barrett P. N., Koschel K. Effect of antibody-induced modulation of measles (SSPE) virus membrane proteins on beta-adrenergic receptor-mediated adenylate cyclase activity. Virology. 1983 Jun;127(2):299–308. doi: 10.1016/0042-6822(83)90145-9. [DOI] [PubMed] [Google Scholar]
- Benda P., Lightbody J., Sato G., Levine L., Sweet W. Differentiated rat glial cell strain in tissue culture. Science. 1968 Jul 26;161(3839):370–371. doi: 10.1126/science.161.3839.370. [DOI] [PubMed] [Google Scholar]
- Chen T. R. In situ detection of mycoplasma contamination in cell cultures by fluorescent Hoechst 33258 stain. Exp Cell Res. 1977 Feb;104(2):255–262. doi: 10.1016/0014-4827(77)90089-1. [DOI] [PubMed] [Google Scholar]
- Curran J., Boeck R., Kolakofsky D. The Sendai virus P gene expresses both an essential protein and an inhibitor of RNA synthesis by shuffling modules via mRNA editing. EMBO J. 1991 Oct;10(10):3079–3085. doi: 10.1002/j.1460-2075.1991.tb07860.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ginzburg I., de Baetselier A., Walker M. D., Behar L., Lehrach H., Frischauf A. M., Littauer U. Z. Brain tubulin and actin cDNA sequences: isolation of recombinant plasmids. Nucleic Acids Res. 1980 Aug 25;8(16):3553–3564. doi: 10.1093/nar/8.16.3553. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Halbach M., Koschel K. Impairment of hormone dependent signal transfer by chronic SSPE virus infection. J Gen Virol. 1979 Mar;42(3):615–619. doi: 10.1099/0022-1317-42-3-615. [DOI] [PubMed] [Google Scholar]
- Hummel K. B., Vanchiere J. A., Bellini W. J. Restriction of fusion protein mRNA as a mechanism of measles virus persistence. Virology. 1994 Aug 1;202(2):665–672. doi: 10.1006/viro.1994.1388. [DOI] [PubMed] [Google Scholar]
- Hyypiä T., Korkiamäki P., Vainionpä R. Replication of measles virus in human lymphocytes. J Exp Med. 1985 Jun 1;161(6):1261–1271. doi: 10.1084/jem.161.6.1261. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Koschel K., Brinckmann U., Hoyningen-Huene V. V. Measles virus antisense sequences specifically cure cells persistently infected with measles virus. Virology. 1995 Feb 20;207(1):168–178. doi: 10.1006/viro.1995.1063. [DOI] [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- Lin H. Y., Kaji E. H., Winkel G. K., Ives H. E., Lodish H. F. Cloning and functional expression of a vascular smooth muscle endothelin 1 receptor. Proc Natl Acad Sci U S A. 1991 Apr 15;88(8):3185–3189. doi: 10.1073/pnas.88.8.3185. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MacCumber M. W., Ross C. A., Snyder S. H. Endothelin in brain: receptors, mitogenesis, and biosynthesis in glial cells. Proc Natl Acad Sci U S A. 1990 Mar;87(6):2359–2363. doi: 10.1073/pnas.87.6.2359. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Malpartida F., Zalacaín M., Jiménez A., Davies J. Molecular cloning and expression in streptomyces lividans of a hygromycin B phosphotransferase gene from Streptomyces hygroscopicus. Biochem Biophys Res Commun. 1983 Nov 30;117(1):6–12. doi: 10.1016/0006-291x(83)91533-4. [DOI] [PubMed] [Google Scholar]
- Matsumoto H., Suzuki N., Onda H., Fujino M. Abundance of endothelin-3 in rat intestine, pituitary gland and brain. Biochem Biophys Res Commun. 1989 Oct 16;164(1):74–80. doi: 10.1016/0006-291x(89)91684-7. [DOI] [PubMed] [Google Scholar]
- Melton D. A., Krieg P. A., Rebagliati M. R., Maniatis T., Zinn K., Green M. R. Efficient in vitro synthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoter. Nucleic Acids Res. 1984 Sep 25;12(18):7035–7056. doi: 10.1093/nar/12.18.7035. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nudel U., Zakut R., Shani M., Neuman S., Levy Z., Yaffe D. The nucleotide sequence of the rat cytoplasmic beta-actin gene. Nucleic Acids Res. 1983 Mar 25;11(6):1759–1771. doi: 10.1093/nar/11.6.1759. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Simonson M. S., Dunn M. J. Cellular signaling by peptides of the endothelin gene family. FASEB J. 1990 Sep;4(12):2989–3000. doi: 10.1096/fasebj.4.12.2168326. [DOI] [PubMed] [Google Scholar]
- Stojilković S. S., Catt K. J. Neuroendocrine actions of endothelins. Trends Pharmacol Sci. 1992 Oct;13(10):385–391. doi: 10.1016/0165-6147(92)90118-p. [DOI] [PubMed] [Google Scholar]
- Tas P. W., Koschel K. Loss of the endothelin signal pathway in C6 rat glioma cells persistently infected with measles virus. Proc Natl Acad Sci U S A. 1991 Aug 1;88(15):6736–6739. doi: 10.1073/pnas.88.15.6736. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vainionpä R., Hyypiä T., Akerman K. E. Early signal transduction in measles virus-infected lymphocytes is unaltered, but second messengers activate virus replication. J Virol. 1991 Dec;65(12):6743–6748. doi: 10.1128/jvi.65.12.6743-6748.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Valsamakis A., Riviere Y., Oldstone M. B. Perturbation of differentiated functions in vivo during persistent viral infection. III. Decreased growth hormone mRNA. Virology. 1987 Feb;156(2):214–220. doi: 10.1016/0042-6822(87)90400-4. [DOI] [PubMed] [Google Scholar]
- Yanagisawa M., Kurihara H., Kimura S., Tomobe Y., Kobayashi M., Mitsui Y., Yazaki Y., Goto K., Masaki T. A novel potent vasoconstrictor peptide produced by vascular endothelial cells. Nature. 1988 Mar 31;332(6163):411–415. doi: 10.1038/332411a0. [DOI] [PubMed] [Google Scholar]
- Zinnheimer-Dreikorn J., Koschel K. P. Antigenic modulation of measles subacute sclerosing panencephalitis virus in a persistently infected rat glioma cell line by monoclonal anti-haemagglutinin antibodies. J Gen Virol. 1990 Jun;71(Pt 6):1391–1394. doi: 10.1099/0022-1317-71-6-1391. [DOI] [PubMed] [Google Scholar]