Abstract
Unfixed, compressed acinar cells of rat pancreas, isolated by mechanical and enzymatic means, were examined by phase microscopy and photomicrographed using 35 mm film and electronic flash illumination. Similarly, observations were made on Walker carcinoma cells; in addition, these cells were treated with solutions containing either phosphatidase A or enzyme inhibitors. Acinar cells contained, besides nuclei, perinuclear droplets and secretion granules, various membranous and vacuolar structures. The basal cytoplasm showed parallel dark lines interpreted as endoplasmic reticulum. In some cells, fragmentation of the reticulum was followed by the direct incorporation of fragments into simple myelin figures. In other cells it appeared that phase-lucent linear structures and vacuoles were derived by dilatation of cisternae of the endoplasmic reticulum. Perinuclear fluid collections arose either by dilation of the perinuclear cisternae of the endoplasmic reticulum or by fluid dilatation of the nuclear envelope. Phosphatidase A disrupted early vacuoles of Walker carcinoma cells. From this and the direct involvement of elements of the endoplasmic reticulum in myelin figures, it was concluded that the membranes limiting the endoplasmic reticulum incorporate phosphatides in continuous layers. While many severely injured cells formed large vacuoles, others developed concentrically laminated myelin figures; it was concluded that both types of structure derived from phosphatides liberated intracellularly, the vacuoles by vesicular myelin figure formation.
Full Text
The Full Text of this article is available as a PDF (2.4 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- BUCHSBAUM R., KUNTZ J. A. The effects of certain stimulants and depresants on individual fibroblasts in a perfusion chamber. Ann N Y Acad Sci. 1954 Nov 17;58(7):1303–1310. doi: 10.1111/j.1749-6632.1954.tb45910.x. [DOI] [PubMed] [Google Scholar]
- DOERY H. M., PEARSON J. E. Haemolysins in venoms of Australian snakes. Observations on the haemolysins of the venoms of some Australian snakes and the separation of phospholipase A from the venom of Pseudechis porphyriacus. Biochem J. 1961 Apr;78:820–827. doi: 10.1042/bj0780820. [DOI] [PMC free article] [PubMed] [Google Scholar]
- EMMELOT P., BENEDETTI E. L. Changes in the fine structure of rat liver cells brought about by dimethylnitrosamine. J Biophys Biochem Cytol. 1960 Apr;7:393–396. doi: 10.1083/jcb.7.2.393. [DOI] [PMC free article] [PubMed] [Google Scholar]
- FAWCETT D. W., ITO S. Observations on the cytoplasmic membranes of testicular cells, examined by phase contrast and electron microscopy. J Biophys Biochem Cytol. 1958 Mar 25;4(2):135–142. doi: 10.1083/jcb.4.2.135. [DOI] [PMC free article] [PubMed] [Google Scholar]
- KUTSAKIS A., LATTA H. Cytotoxic effects of specific antiserum and 17-hydroxycorticosterone on cells in tissue culture. Lab Invest. 1957 Jan-Feb;6(1):12–27. [PubMed] [Google Scholar]
- MORGAN C., HOWE C., ROSE H. M. Structure and development of viruses as observed in the electron microscope. V. Western equine encephalomyelitis virus. J Exp Med. 1961 Jan 1;113:219–234. doi: 10.1084/jem.113.1.219. [DOI] [PMC free article] [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]
- PALADE G. E., SIEKEVITZ P. Liver microsomes; an integrated morphological and biochemical study. J Biophys Biochem Cytol. 1956 Mar 25;2(2):171–200. doi: 10.1083/jcb.2.2.171. [DOI] [PMC free article] [PubMed] [Google Scholar]
- PALADE G. E., SIEKEVITZ P. Pancreatic microsomes; an integrated morphological and biochemical study. J Biophys Biochem Cytol. 1956 Nov 25;2(6):671–690. doi: 10.1083/jcb.2.6.671. [DOI] [PMC free article] [PubMed] [Google Scholar]
- PALAY S. L., WISSIG S. L. Secretory granules and Nissl substance in fresh supraoptic neurones of the rabbit. Anat Rec. 1953 Jul;116(3):301–313. doi: 10.1002/ar.1091160307. [DOI] [PubMed] [Google Scholar]
- PORTER K. R. Observations on a submicroscopic basophilic component of cytoplasm. J Exp Med. 1953 May;97(5):727–750. doi: 10.1084/jem.97.5.727. [DOI] [PMC free article] [PubMed] [Google Scholar]
- REVEL J. P., ITO S., FAWCETT D. W. Electron micrographs of myelin figures of phospholipide simulating intracellular membranes. J Biophys Biochem Cytol. 1958 Jul 25;4(4):495–498. doi: 10.1083/jcb.4.4.495. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ROSE G. G., POMERAT C. M. Phase contrast observations of the endoplasmic reticulum in living tissue cultures. J Biophys Biochem Cytol. 1960 Oct;8:423–430. doi: 10.1083/jcb.8.2.423. [DOI] [PMC free article] [PubMed] [Google Scholar]
- STOECKENIUS W. An electron microscope study of myelin figures. J Biophys Biochem Cytol. 1959 May 25;5(3):491–500. doi: 10.1083/jcb.5.3.491. [DOI] [PMC free article] [PubMed] [Google Scholar]
- WEISS J. M. The ergastoplasm; its fine structure and relation to protein synthesis as studied with the electron microscope in the pancreas of the Swiss albino mouse. J Exp Med. 1953 Dec;98(6):607–618. doi: 10.1084/jem.98.6.607. [DOI] [PMC free article] [PubMed] [Google Scholar]
