Abstract
Treatment of hepatocyte-hepatoma hybrid cells with Clostridium botulinum C2 toxin led to a 167% increase in monomeric globular actin (G-actin) and to a 57% decrease in filamentous actin (F-actin) within 2 h. Simultaneously, the level of actin mRNA was specifically decreased to 49% and actin synthesis was significantly diminished. In contrast, treatment of hybrid cells with phalloidin led to a decrease in G-actin to 55% and to a reciprocal increase in actin mRNA to 244% and an increase in actin synthesis. These alterations of actin synthesis depending on the G-actin/F-actin ratio corresponded to the autoregulation of actin synthesis observed in primary cultures of rat hepatocytes. Microinjection of C2 toxin or of phalloidin into hepatocyte-hepatoma hybrid cells had the same effects on actin synthesis as incubation with either toxin in the culture medium. Microinjection of nonpolymerizable ADP-ribosylated G-actin into hepatocyte-hepatoma hybrid cells specifically decreased the incorporation of [35S]methionine into newly synthesized actin within 1 h. This decrease continued for at least 19 h. Microinjection of ADP-ribosylated actin led to rounding of cells and obvious disaggregation of actin filaments, which might be due to capping of actin filaments by the ADP-ribosylated actin. Because stabilization of actin filaments by phalloidin before microinjection of ADP-ribosylated actin also resulted in decreased actin synthesis, the concentration of monomeric G-actin seems to be responsible for the regulation of actin synthesis in hepatocyte-hepatoma hybrid cells, which can be regarded as immortalized hepatocytes.
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- Aktories K., Bärmann M., Ohishi I., Tsuyama S., Jakobs K. H., Habermann E. Botulinum C2 toxin ADP-ribosylates actin. Nature. 1986 Jul 24;322(6077):390–392. doi: 10.1038/322390a0. [DOI] [PubMed] [Google Scholar]
- Aktories K., Reuner K. H., Presek P., Bärmann M. Botulinum C2 toxin treatment increases the G-actin pool in intact chicken cells: a model for the cytopathic action of actin-ADP-ribosylating toxins. Toxicon. 1989;27(9):989–993. doi: 10.1016/0041-0101(89)90149-9. [DOI] [PubMed] [Google Scholar]
- Aktories K., Wegner A. ADP-ribosylation of actin by clostridial toxins. J Cell Biol. 1989 Oct;109(4 Pt 1):1385–1387. doi: 10.1083/jcb.109.4.1385. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bershadsky A. D., Glück U., Denisenko O. N., Sklyarova T. V., Spector I., Ben-Ze'ev A. The state of actin assembly regulates actin and vinculin expression by a feedback loop. J Cell Sci. 1995 Mar;108(Pt 3):1183–1193. doi: 10.1242/jcs.108.3.1183. [DOI] [PubMed] [Google Scholar]
- Blikstad I., Carlsson L. On the dynamics of the microfilament system in HeLa cells. J Cell Biol. 1982 Apr;93(1):122–128. doi: 10.1083/jcb.93.1.122. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Blikstad I., Markey F., Carlsson L., Persson T., Lindberg U. Selective assay of monomeric and filamentous actin in cell extracts, using inhibition of deoxyribonuclease I. Cell. 1978 Nov;15(3):935–943. doi: 10.1016/0092-8674(78)90277-5. [DOI] [PubMed] [Google Scholar]
- Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1016/0003-2697(76)90527-3. [DOI] [PubMed] [Google Scholar]
- Cao L. G., Babcock G. G., Rubenstein P. A., Wang Y. L. Effects of profilin and profilactin on actin structure and function in living cells. J Cell Biol. 1992 Jun;117(5):1023–1029. doi: 10.1083/jcb.117.5.1023. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cao L. G., Fishkind D. J., Wang Y. L. Localization and dynamics of nonfilamentous actin in cultured cells. J Cell Biol. 1993 Oct;123(1):173–181. doi: 10.1083/jcb.123.1.173. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chomczynski P., Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem. 1987 Apr;162(1):156–159. doi: 10.1006/abio.1987.9999. [DOI] [PubMed] [Google Scholar]
- Cleveland D. W., Pittenger M. F., Feramisco J. R. Elevation of tubulin levels by microinjection suppresses new tubulin synthesis. Nature. 1983 Oct 20;305(5936):738–740. doi: 10.1038/305738a0. [DOI] [PubMed] [Google Scholar]
- Cooper J. A., Bryan J., Schwab B., 3rd, Frieden C., Loftus D. J., Elson E. L. Microinjection of gelsolin into living cells. J Cell Biol. 1987 Mar;104(3):491–501. doi: 10.1083/jcb.104.3.491. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cooper J. A. Effects of cytochalasin and phalloidin on actin. J Cell Biol. 1987 Oct;105(4):1473–1478. doi: 10.1083/jcb.105.4.1473. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cooper J. A. The role of actin polymerization in cell motility. Annu Rev Physiol. 1991;53:585–605. doi: 10.1146/annurev.ph.53.030191.003101. [DOI] [PubMed] [Google Scholar]
- Feldmann G. The cytoskeleton of the hepatocyte. Structure and functions. J Hepatol. 1989 May;8(3):380–386. doi: 10.1016/0168-8278(89)90038-x. [DOI] [PubMed] [Google Scholar]
- Füchtbauer A., Jockusch B. M., Maruta H., Kilimann M. W., Isenberg G. Disruption of microfilament organization after injection of F-actin capping proteins into living tissue culture cells. 1983 Jul 28-Aug 3Nature. 304(5924):361–364. doi: 10.1038/304361a0. [DOI] [PubMed] [Google Scholar]
- Graessmann A., Graessmann M., Mueller C. Microinjection of early SV40 DNA fragments and T antigen. Methods Enzymol. 1980;65(1):816–825. doi: 10.1016/s0076-6879(80)65076-9. [DOI] [PubMed] [Google Scholar]
- Heacock C. S., Bamburg J. R. The quantitation of G- and F-actin in cultured cells. Anal Biochem. 1983 Nov;135(1):22–36. doi: 10.1016/0003-2697(83)90725-x. [DOI] [PubMed] [Google Scholar]
- Hooser S. B., Beasley V. R., Waite L. L., Kuhlenschmidt M. S., Carmichael W. W., Haschek W. M. Actin filament alterations in rat hepatocytes induced in vivo and in vitro by microcystin-LR, a hepatotoxin from the blue-green alga, Microcystis aeruginosa. Vet Pathol. 1991 Jul;28(4):259–266. doi: 10.1177/030098589102800401. [DOI] [PubMed] [Google Scholar]
- Katz N. R., Giffhorn S. Glucose- and insulin-independent induction of ATP citrate lyase in primary cultures of rat hepatocytes. Biochem J. 1983 Apr 15;212(1):65–71. doi: 10.1042/bj2120065. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Katz N., Immenschuh S., Gerbracht U., Eigenbrodt E., Föllmann W., Petzinger E. Hormone-sensitive carbohydrate metabolism in rat hepatocyte-hepatoma hybrid cells. Eur J Cell Biol. 1992 Feb;57(1):117–123. [PubMed] [Google Scholar]
- Kreis T. E., Geiger B., Schlessinger J. Mobility of microinjected rhodamine actin within living chicken gizzard cells determined by fluorescence photobleaching recovery. Cell. 1982 Jul;29(3):835–845. doi: 10.1016/0092-8674(82)90445-7. [DOI] [PubMed] [Google Scholar]
- Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
- Leavitt J., Ng S. Y., Aebi U., Varma M., Latter G., Burbeck S., Kedes L., Gunning P. Expression of transfected mutant beta-actin genes: alterations of cell morphology and evidence for autoregulation in actin pools. Mol Cell Biol. 1987 Jul;7(7):2457–2466. doi: 10.1128/mcb.7.7.2457. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lloyd C., Schevzov G., Gunning P. Transfection of nonmuscle beta- and gamma-actin genes into myoblasts elicits different feedback regulatory responses from endogenous actin genes. J Cell Biol. 1992 May;117(4):787–797. doi: 10.1083/jcb.117.4.787. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Müller H., von Eichel-Streiber C., Habermann E. Morphological changes of cultured endothelial cells after microinjection of toxins that act on the cytoskeleton. Infect Immun. 1992 Jul;60(7):3007–3010. doi: 10.1128/iai.60.7.3007-3010.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Neuhaus J. M., Wanger M., Keiser T., Wegner A. Treadmilling of actin. J Muscle Res Cell Motil. 1983 Oct;4(5):507–527. doi: 10.1007/BF00712112. [DOI] [PubMed] [Google Scholar]
- Ohishi I., Iwasaki M., Sakaguchi G. Purification and characterization of two components of botulinum C2 toxin. Infect Immun. 1980 Dec;30(3):668–673. doi: 10.1128/iai.30.3.668-673.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Petzinger E., Föllmann W., Blumrich M., Walther P., Hentschel J., Bette P., Maurice M., Feldmann G. Immortalization of rat hepatocytes by fusion with hepatoma cells. I. Cloning of a hepatocytoma cell line with bile canaliculi. Eur J Cell Biol. 1994 Aug;64(2):328–338. [PubMed] [Google Scholar]
- Pollard T. D., Cooper J. A. Actin and actin-binding proteins. A critical evaluation of mechanisms and functions. Annu Rev Biochem. 1986;55:987–1035. doi: 10.1146/annurev.bi.55.070186.005011. [DOI] [PubMed] [Google Scholar]
- Polokoff M. A., Everson G. T. Hepatocyte-hepatoma cell hybrids. Characterization and demonstration of bile acid synthesis. J Biol Chem. 1986 Mar 25;261(9):4085–4089. [PubMed] [Google Scholar]
- Rao K. M., Betschart J. M., Virji M. A. Hormone-induced actin polymerization in rat hepatoma cells and human leucocytes. Biochem J. 1985 Sep 15;230(3):709–714. doi: 10.1042/bj2300709. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Reuner K. H., Presek P., Boschek C. B., Aktories K. Botulinum C2 toxin ADP-ribosylates actin and disorganizes the microfilament network in intact cells. Eur J Cell Biol. 1987 Feb;43(1):134–140. [PubMed] [Google Scholar]
- Reuner K. H., Schlegel K., Just I., Aktories K., Katz N. Autoregulatory control of actin synthesis in cultured rat hepatocytes. FEBS Lett. 1991 Jul 29;286(1-2):100–104. doi: 10.1016/0014-5793(91)80950-8. [DOI] [PubMed] [Google Scholar]
- Reuner K. H., Wiederhold M., Dunker P., Just I., Bohle R. M., Kröger M., Katz N. Autoregulation of actin synthesis in hepatocytes by transcriptional and posttranscriptional mechanisms. Eur J Biochem. 1995 May 15;230(1):32–37. doi: 10.1111/j.1432-1033.1995.0032i.x. [DOI] [PubMed] [Google Scholar]
- Serpinskaya A. S., Denisenko O. N., Gelfand V. I., Bershadsky A. D. Stimulation of actin synthesis in phalloidin-treated cells. Evidence for autoregulatory control. FEBS Lett. 1990 Dec 17;277(1-2):11–14. doi: 10.1016/0014-5793(90)80797-m. [DOI] [PubMed] [Google Scholar]
- Sklyarova T., Kostyukovski V., Sharov V., Prisyazhnoy V., Denisenko O. Alterations in protein synthesis induced by C2 toxin in 3T3 cells. FEBS Lett. 1995 Apr 24;363(3):273–276. doi: 10.1016/0014-5793(95)00329-8. [DOI] [PubMed] [Google Scholar]
- Snabes M. C., Boyd A. E., 3rd, Pardue R. L., Bryan J. A DNase I binding/immunoprecipitation assay for actin. J Biol Chem. 1981 Jun 25;256(12):6291–6295. [PubMed] [Google Scholar]
- Spudich J. A., Watt S. The regulation of rabbit skeletal muscle contraction. I. Biochemical studies of the interaction of the tropomyosin-troponin complex with actin and the proteolytic fragments of myosin. J Biol Chem. 1971 Aug 10;246(15):4866–4871. [PubMed] [Google Scholar]
- Stacey D. W., Allfrey V. G. Microinjection studies of duck globin messenger RNA translation in human and avian cells. Cell. 1976 Dec;9(4 Pt 2):725–732. doi: 10.1016/0092-8674(76)90136-7. [DOI] [PubMed] [Google Scholar]
- Stiles B. G., Wilkins T. D. Purification and characterization of Clostridium perfringens iota toxin: dependence on two nonlinked proteins for biological activity. Infect Immun. 1986 Dec;54(3):683–688. doi: 10.1128/iai.54.3.683-688.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Suttorp N., Polley M., Seybold J., Schnittler H., Seeger W., Grimminger F., Aktories K. Adenosine diphosphate-ribosylation of G-actin by botulinum C2 toxin increases endothelial permeability in vitro. J Clin Invest. 1991 May;87(5):1575–1584. doi: 10.1172/JCI115171. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Symons M. H., Mitchison T. J. Control of actin polymerization in live and permeabilized fibroblasts. J Cell Biol. 1991 Aug;114(3):503–513. doi: 10.1083/jcb.114.3.503. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Theodoropoulos P. A., Stournaras C., Stoll B., Markogiannakis E., Lang F., Gravanis A., Häussinger D. Hepatocyte swelling leads to rapid decrease of the G-/total actin ratio and increases actin mRNA levels. FEBS Lett. 1992 Oct 26;311(3):241–245. doi: 10.1016/0014-5793(92)81111-x. [DOI] [PubMed] [Google Scholar]
- Wegner A., Aktories K. ADP-ribosylated actin caps the barbed ends of actin filaments. J Biol Chem. 1988 Sep 25;263(27):13739–13742. [PubMed] [Google Scholar]
- Wegner A. Head to tail polymerization of actin. J Mol Biol. 1976 Nov;108(1):139–150. doi: 10.1016/s0022-2836(76)80100-3. [DOI] [PubMed] [Google Scholar]
- Wiener J., Loud A. V., Kimberg D. V., Spiro D. A quantitative description of cortisone-induced alterations in the ultrastructure of rat liver parenchmal cells. J Cell Biol. 1968 Apr;37(1):47–61. doi: 10.1083/jcb.37.1.47. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wysolmerski R. B., Lagunoff D. Inhibition of endothelial cell retraction by ATP depletion. Am J Pathol. 1988 Jul;132(1):28–37. [PMC free article] [PubMed] [Google Scholar]
