Abstract
The effects of the ionophoric antibiotic X537A on cell structure were studied with phase-contrast, fluorescence, and electron microscopy. X537A induced selective vacuolation of the Golgi apparatus of vascular and intestinal smooth muscle, epithelium, plasma cells, and cultured chick heart and guinea pig vascular smooth muscle cells. The swelling of the Golgi apparatus induced by X537A was reversible in the systems examined for reversibility: vascular smooth muscle and cultured chick heart. Myelin figures were common in the Golgi apparatus vacuolated by X537A. Fluorescence microscopy of cultured cells incubated with X537A showed the characteristic blue X537A fluorescence associated with lipid globules in the cultured cells. Incubation of cultured chick heart cells with X537A reduced the beating rate and, after 24-72 h, abolished the sarcomere pattern. The swelling of the Golgi membranes produced by X537A in cultured vascular smooth muscle was associated with inhibition of D-[6-3H]glucosamine and [35S]sulfate incorporation into glycosaminoglycans.
Full Text
The Full Text of this article is available as a PDF (6.9 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Beams H. W., Kessel R. G. The Golgi apparatus: structure and function. Int Rev Cytol. 1968;23:209–276. doi: 10.1016/s0074-7696(08)60273-9. [DOI] [PubMed] [Google Scholar]
- Bennett G., Leblond C. P., Haddad A. Migration of glycoprotein from the Golgi apparatus to the surface of various cell types as shown by radioautography after labelled fucose injection into rats. J Cell Biol. 1974 Jan;60(1):258–284. doi: 10.1083/jcb.60.1.258. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Caswell A. H., Pressman B. C. Kinetics of transport of divalent cations across sarcoplasmic reticulum vesicles induced by ionophores. Biochem Biophys Res Commun. 1972 Oct 6;49(1):292–298. doi: 10.1016/0006-291x(72)90043-5. [DOI] [PubMed] [Google Scholar]
- Chacko S. DNA synthesis, mitosis, and differentiation in cardiac myogenesis. Dev Biol. 1973 Nov;35(1):1–18. doi: 10.1016/0012-1606(73)90002-x. [DOI] [PubMed] [Google Scholar]
- Chacko S., Joseph X. The effect of 5-bromodeoxyuridine (BrdU) on cardiac muscle differentiation. Dev Biol. 1974 Oct;40(2):340–354. doi: 10.1016/0012-1606(74)90135-3. [DOI] [PubMed] [Google Scholar]
- Daniel J. C., Kosher R. A., Hamos J. E., Lash J. W. Influence of external potassium on the synthesis and deposition of matrix components by chondrocytes in vitro. J Cell Biol. 1974 Dec;63(3):843–854. doi: 10.1083/jcb.63.3.843. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Devine C. E., Somlyo A. V., Somlyo A. P. Sarcoplasmic reticulum and excitation-contraction coupling in mammalian smooth muscles. J Cell Biol. 1972 Mar;52(3):690–718. doi: 10.1083/jcb.52.3.690. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Entman M. L., Gillette P. C., Wallick E. T., Pressman B. C., Schwartz A. A study of calcium binding and uptake by isolated cardiac sarcoplasmic reticulum: the use of a new ionophore (X537A). Biochem Biophys Res Commun. 1972 Aug 21;48(4):847–853. doi: 10.1016/0006-291x(72)90685-7. [DOI] [PubMed] [Google Scholar]
- Entman M. L., Schwartz A. Calcium in the control of cardiac contraction and relaxation: the cardiac relaxing system (sarcoplasmic reticulum fragments) and the effects of ionophoric antibiotics. Recent Adv Stud Cardiac Struct Metab. 1974;4:437–450. [PubMed] [Google Scholar]
- Estrada S., Célis H., Calderón E., Gallo G., Montal M. Model translocators for divalent and monovalent ion transport in phospholipid membranes. II. The effects of ion translocator X-537A on the energy-conserving properties of mitochondrial membranes. J Membr Biol. 1974;18(3-4):201–218. doi: 10.1007/BF01870112. [DOI] [PubMed] [Google Scholar]
- Farquhar M. G., Bergeron J. J., Palade G. E. Cytochemistry of Golgi fractions prepared from rat liver. J Cell Biol. 1974 Jan;60(1):8–25. doi: 10.1083/jcb.60.1.8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fleischer B., Fleischer S. Preparation and characterization of golgi membranes from rat liver. Biochim Biophys Acta. 1970 Dec 1;219(2):301–319. doi: 10.1016/0005-2736(70)90209-9. [DOI] [PubMed] [Google Scholar]
- Jamieson J. D., Palade G. E. Intracellular transport of secretory proteins in the pancreatic exocrine cell. II. Transport to condensing vacuoles and zymogen granules. J Cell Biol. 1967 Aug;34(2):597–615. doi: 10.1083/jcb.34.2.597. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jamieson J. D., Palade G. E. Role of the Golgi complex in the intracellular transport of secretory proteins. Proc Natl Acad Sci U S A. 1966 Feb;55(2):424–431. doi: 10.1073/pnas.55.2.424. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jones A. W., Somlyo A. P., Somlyo A. V. Potassium accumulation in smooth muscle and associated ultrastructural changes. J Physiol. 1973 Jul;232(2):247–273. doi: 10.1113/jphysiol.1973.sp010268. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kletzien R. F., Perdue J. F. Sugar transport in chick embryo fibroblasts. I. A functional change in the plasma membrane associated with the rate of cell growth. J Biol Chem. 1974 Jun 10;249(11):3366–3374. [PubMed] [Google Scholar]
- Kushmerick M. J., Larson R. E., Davies R. E. The chemical energetics of muscle contraction. I. Activation heat, heat of shortening and ATP utilization for activation-relaxation processes. Proc R Soc Lond B Biol Sci. 1969 Dec 23;174(1036):293–313. doi: 10.1098/rspb.1969.0095. [DOI] [PubMed] [Google Scholar]
- Levy J. V., Cohen J. A., Inesi G. Contractile effects of a calcium ionophore. Nature. 1973 Apr 13;242(5398):461–463. doi: 10.1038/242461a0. [DOI] [PubMed] [Google Scholar]
- Lin D. C., Kun E. Mode of action of the antibiotic X-537A on mitochondrial glutamate oxidation. Biochem Biophys Res Commun. 1973 Feb 5;50(3):820–825. doi: 10.1016/0006-291x(73)91318-1. [DOI] [PubMed] [Google Scholar]
- Nameroff M., Holtzer H. The loss of phenotypic traits by differentiated cells. IV. Changes in polysaccharides produced by dividing chondrocytes. Dev Biol. 1967 Sep;16(3):250–281. doi: 10.1016/0012-1606(67)90026-7. [DOI] [PubMed] [Google Scholar]
- PALADE G. E., CLAUDE A. The nature of the Golgi apparatus; identification of the Golgi apparatus with a complex of myelin figures. J Morphol. 1949 Jul;85(1):71–111. doi: 10.1002/jmor.1050850104. [DOI] [PubMed] [Google Scholar]
- PALADE G. E., CLAUDE A. The nature of the Golgi apparatus; parallelism between intercellular myelin figures and Golgi apparatus in somatic cells. J Morphol. 1949 Jul;85(1):35–69. doi: 10.1002/jmor.1050850103. [DOI] [PubMed] [Google Scholar]
- Pelletier G. Autoradiographic studies of synthesis and intracellular migration of glycoproteins in the rat anterior pituitary gland. J Cell Biol. 1974 Jul;62(1):185–197. doi: 10.1083/jcb.62.1.185. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pressman B. C., De Guzman N. T. New ionophores for old organelles. Ann N Y Acad Sci. 1974 Feb 18;227:380–391. doi: 10.1111/j.1749-6632.1974.tb14401.x. [DOI] [PubMed] [Google Scholar]
- Pressman B. C. Properties of ionophores with broad range cation selectivity. Fed Proc. 1973 Jun;32(6):1698–1703. [PubMed] [Google Scholar]
- REVEL J. P., HAY E. D. AN AUTORADIOGRAPHIC AND ELECTRON MICROSCOPIC STUDY OF COLLAGEN SYNTHESIS IN DIFFERENTIATING CARTILAGE. Z Zellforsch Mikrosk Anat. 1963 Oct 8;61:110–144. doi: 10.1007/BF00341524. [DOI] [PubMed] [Google Scholar]
- Ross R., Klebanoff S. J. The smooth muscle cell. I. In vivo synthesis of connective tissue proteins. J Cell Biol. 1971 Jul;50(1):159–171. doi: 10.1083/jcb.50.1.159. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schaffer S. W., Safer B., Scarpa A., Williamson J. R. Mode of action of the calcium ionophores X-537A and A23187 on cardiac contractility. Biochem Pharmacol. 1974 May 1;23(11):1609–1617. doi: 10.1016/0006-2952(74)90373-6. [DOI] [PubMed] [Google Scholar]
- Somlyo A. P., Devine C. E., Somlyo A. V., Rice R. V. Filament organization in vertebrate smooth muscle. Philos Trans R Soc Lond B Biol Sci. 1973 Mar 15;265(867):223–229. doi: 10.1098/rstb.1973.0027. [DOI] [PubMed] [Google Scholar]
- Somlyo A. P., Somlyo A. V. Vascular smooth muscle. I. Normal structure, pathology, biochemistry, and biophysics. Pharmacol Rev. 1968 Dec;20(4):197–272. [PubMed] [Google Scholar]
- Somlyo A. P., Somlyo A. V. Vascular smooth muscle. II. Pharmacology of normal and hypotensive vessels. Pharmacol Rev. 1970 Jun;22(2):249–353. [PubMed] [Google Scholar]
- Somlyo A. V., Somlyo A. P. Strontium accumulation by sarcoplasmic reticulum and mitochondria in vascular smooth muscle. Science. 1971 Nov 26;174(4012):955–958. doi: 10.1126/science.174.4012.955. [DOI] [PubMed] [Google Scholar]
- Spurr A. R. A low-viscosity epoxy resin embedding medium for electron microscopy. J Ultrastruct Res. 1969 Jan;26(1):31–43. doi: 10.1016/s0022-5320(69)90033-1. [DOI] [PubMed] [Google Scholar]
- Weinstock M., Leblond C. P. Synthesis, migration, and release of precursor collagen by odontoblasts as visualized by radioautography after (3H)proline administration. J Cell Biol. 1974 Jan;60(1):92–127. doi: 10.1083/jcb.60.1.92. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Westley J. W., Oliveto E. P., Berger J., Evans R. H., Jr, Glass R., Stempel A., Toome V., Williams T. Chemical transformations of antibiotic X-537A and their effect on antibacterial activity. J Med Chem. 1973 Apr;16(4):397–403. doi: 10.1021/jm00262a020. [DOI] [PubMed] [Google Scholar]
- Whaley W. G., Dauwalder M., Kephart J. E. Golgi apparatus: influence on cell surfaces. Science. 1972 Feb 11;175(4022):596–599. doi: 10.1126/science.175.4022.596. [DOI] [PubMed] [Google Scholar]
- Whetsell W. O., Jr, Bunge R. P. Reversible alterations in the Golgi complex of cultured neurons treated with an inhibitor of active Na and K transport. J Cell Biol. 1969 Aug;42(2):490–500. doi: 10.1083/jcb.42.2.490. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Williamson J. R., Schaffer S. W., Scarpa A., Safer B. Investigation of the calcium cycle in perfused rat and frog hearts. Recent Adv Stud Cardiac Struct Metab. 1974;4:375–392. [PubMed] [Google Scholar]
