Abstract
The dependence of cytoplasmic membranes upon the nucleus was studied by examining enucleated amebae with the electron microscope at intervals up to 1 wk after enucleation. Amebae were cut into two approximately equal parts, and the fine structure of the enucleated portions was compared with that of the nucleated parts and starved whole cells which had been maintained under the same conditions. Golgi bodies were diminished in size 1 day after enucleation and were not detected in cells enucleated for more than 2 days. The endoplasmic reticulum of enucleated cells appeared to increase in amount and underwent changes in its morphology. The sparsely scattered short tubules of granular endoplasmic reticulum present in unmanipulated amebae from stock cultures were replaced in 1–3-day enucleates by long narrow cisternae. In 3–7-day enucleates, similar cisternae of granular endoplasmic reticulum encircled areas of cytoplasm partially or completely. It was estimated that in most cases hundreds of these areas encircled by two rough membranes were formed per enucleated cell. The number of ribosomes studding the surface of the endoplasmic reticulum decreased progressively with time after enucleation. In contrast, the membranes of nucleated parts and starved whole cells did not undergo these changes. The possible identification of membrane-encircled areas as cytolysomes and their mode of formation are considered. Implications of the observations regarding nuclear regulation of the form of the Golgi apparatus and the endoplasmic reticulum are discussed.
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Selected References
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- ASHFORD T. P., PORTER K. R. Cytoplasmic components in hepatic cell lysosomes. J Cell Biol. 1962 Jan;12:198–202. doi: 10.1083/jcb.12.1.198. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BRACHET J. New observations on biochemical interactions between nucleus and cytoplasm in Amoeba and Acetabularia. Exp Cell Res. 1959;Suppl 6:78–96. [PubMed] [Google Scholar]
- BRACHET J. Recherches sur les interactions biochimiques entre le noyau et le cytoplasme chez les organismes unicellulaires. I. Amoeba proteus. Biochim Biophys Acta. 1955 Oct;18(2):247–268. doi: 10.1016/0006-3002(55)90063-9. [DOI] [PubMed] [Google Scholar]
- BRANDES D., BERTINI F. ROLE OF GOLGI APPARATUS IN THE FORMATION OF CYTOLYSOMES. Exp Cell Res. 1964 Jun;35:194–197. doi: 10.1016/0014-4827(64)90081-3. [DOI] [PubMed] [Google Scholar]
- De Duve C., Wattiaux R. Functions of lysosomes. Annu Rev Physiol. 1966;28:435–492. doi: 10.1146/annurev.ph.28.030166.002251. [DOI] [PubMed] [Google Scholar]
- ELLIOTT A. M., BAK I. J. THE FATE OF MITOCHONDRIA DURING AGING IN TETRAHYMENA PYRIFORMIS. J Cell Biol. 1964 Jan;20:113–129. doi: 10.1083/jcb.20.1.113. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ERICSSON J. L., TRUMP B. F., WEIBEL J. ELECTRON MICROSCOPIC STUDIES OF THE PROXIMAL TUBULE OF THE RAT KIDNEY. II. CYTOSEGRESOMES AND CYTOSOMES: THEIR RELATIONSHIP TO EACH OTHER AND TO THE LYSOSOME CONCEPT. Lab Invest. 1965 Jul;14:1341–1365. [PubMed] [Google Scholar]
- GIBOR A., GRANICK S. PLASTIDS AND MITOCHONDRIA: INHERITABLE SYSTEMS. Science. 1964 Aug 14;145(3633):890–897. doi: 10.1126/science.145.3635.890. [DOI] [PubMed] [Google Scholar]
- HRUBAN Z., SWIFT H., WISSLER R. W. Analog-induced inclusions in pancreatic acinar cells. J Ultrastruct Res. 1962 Oct;7:273–285. doi: 10.1016/s0022-5320(62)90023-0. [DOI] [PubMed] [Google Scholar]
- LUCK D. F. FORMATION OF MITOCHONDRIA IN NEUROSPORA CRASSA. A STUDY BASED ON MITOCHONDRIAL DENSITY CHANGES. J Cell Biol. 1965 Mar;24:461–470. doi: 10.1083/jcb.24.3.461. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LUCK D. J. Formation of mitochondria in Neurospora crassa. A quantitative radioautographic study. J Cell Biol. 1963 Mar;16:483–499. doi: 10.1083/jcb.16.3.483. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MAZIA D., PRESCOTT D. M. The role of the nucleus in protein synthesis in Amoeba. Biochim Biophys Acta. 1955 May;17(1):23–34. doi: 10.1016/0006-3002(55)90316-4. [DOI] [PubMed] [Google Scholar]
- MILLER F., PALADE G. E. LYTIC ACTIVITIES IN RENAL PROTEIN ABSORPTION DROPLETS. AN ELECTRON MICROSCOPICAL CYTOCHEMICAL STUDY. J Cell Biol. 1964 Dec;23:519–552. doi: 10.1083/jcb.23.3.519. [DOI] [PMC free article] [PubMed] [Google Scholar]
- NAPOLITANO L. CYTOLYSOMES IN METABOLICALLY ACTIVE CELLS. J Cell Biol. 1963 Aug;18:478–481. doi: 10.1083/jcb.18.2.478. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ROTH L. E., DANIELS E. W. Infective organisms in the cytoplasm of Amoeba proteus. J Biophys Biochem Cytol. 1961 Feb;9:317–323. doi: 10.1083/jcb.9.2.317. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ROTH T. F., PORTER K. R. YOLK PROTEIN UPTAKE IN THE OOCYTE OF THE MOSQUITO AEDES AEGYPTI. L. J Cell Biol. 1964 Feb;20:313–332. doi: 10.1083/jcb.20.2.313. [DOI] [PMC free article] [PubMed] [Google Scholar]
- TRUMP B. F., GOLDBLATT P. J., STOWELL R. E. An electron microscopic study of early cytoplasmic alterations in hepatic parenchymal cells of mouse liver during necrosis in vitro (autolysis). Lab Invest. 1962 Nov;11:986–1015. [PubMed] [Google Scholar]
- VENABLE J. H., COGGESHALL R. A SIMPLIFIED LEAD CITRATE STAIN FOR USE IN ELECTRON MICROSCOPY. J Cell Biol. 1965 May;25:407–408. doi: 10.1083/jcb.25.2.407. [DOI] [PMC free article] [PubMed] [Google Scholar]
