Abstract
The dynamics of plasma membrane retrieval has been studied in the pancreatic acinar carcinoma in order to determine if neoplastic cells exhibiting a heterogeneity of cytodifferentiation states retain the capacity to interiorize and recycle plasma membrane. To this end, the plasma membranes of neoplastic pancreatic acinar cells were labeled with radioiodinated cationic ferritin (125I-CF), and the fate of the tracer was monitored by quantitative electron microscopic autoradiography. The undifferentiated granule-deficient cells of the tumor internalized membrane-bound 125I-CF and sequestered it predominantly in lysosomes. By contrast, the differentiated granule-rich cells internalized significantly more membrane-bound 125I-CF, and the tracer was localized in secretory granules and in lysosomes. The data suggest that neoplastic cells retain the capability of retrieving plasma membrane and that the dynamics of the process is correlated with the state of cytodifferentiation of the neoplastic cells.
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- Becich M. J., Bendayan M., Reddy J. K. Intracellular transport and storage of secretory proteins in relation to cytodifferentiation in neoplastic pancreatic acinar cells. J Cell Biol. 1983 Apr;96(4):949–960. doi: 10.1083/jcb.96.4.949. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Becich M. J., Reddy J. K. Separation and characterization of neoplastic cell subpopulations of a transplantable rat pancreatic acinar carcinoma. Cancer Res. 1982 Sep;42(9):3729–3740. [PubMed] [Google Scholar]
- Ceccarelli B., Hurlbut W. P., Mauro A. Turnover of transmitter and synaptic vesicles at the frog neuromuscular junction. J Cell Biol. 1973 May;57(2):499–524. doi: 10.1083/jcb.57.2.499. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Farquhar M. G. Recovery of surface membrane in anterior pituitary cells. Variations in traffic detected with anionic and cationic ferritin. J Cell Biol. 1978 Jun;77(3):R35–R42. doi: 10.1083/jcb.77.3.r35. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Geuze J. J., Kramer M. F. Function of coated membranes and multivesicular bodies during membrane regulation in stimulated exocrine pancreas cells. Cell Tissue Res. 1974;156(1):1–20. doi: 10.1007/BF00220098. [DOI] [PubMed] [Google Scholar]
- Gonatas J., Stieber A., Olsnes S., Gonatas N. K. Pathways involved in fluid phase and adsorptive endocytosis in neuroblastoma. J Cell Biol. 1980 Dec;87(3 Pt 1):579–588. doi: 10.1083/jcb.87.3.579. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hansen L. J., Reddy M. K., Reddy J. K. Comparison of secretory protein and membrane composition of secretory granules isolated from normal and neoplastic pancreatic acinar cells of rats. Proc Natl Acad Sci U S A. 1983 Jul;80(14):4379–4383. doi: 10.1073/pnas.80.14.4379. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Herzog V., Farquhar M. G. Luminal membrane retrieved after exocytosis reaches most golgi cisternae in secretory cells. Proc Natl Acad Sci U S A. 1977 Nov;74(11):5073–5077. doi: 10.1073/pnas.74.11.5073. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Herzog V., Miller F. Membrane retrieval in epithelial cells of isolated thyroid follicles. Eur J Cell Biol. 1979 Aug;19(3):203–215. [PubMed] [Google Scholar]
- Herzog V., Reggio H. Pathways of endocytosis from luminal plasma membrane in rat exocrine pancreas. Eur J Cell Biol. 1980 Jun;21(2):141–150. [PubMed] [Google Scholar]
- Holtzman E., Teichberg S., Abrahams S. J., Citkowitz E., Crain S. M., Kawai N., Peterson E. R. Notes on synaptic vesicles and related structures, endoplasmic reticulum, lysosomes and peroxisomes in nervous tissue and the adrenal medulla. J Histochem Cytochem. 1973 Apr;21(4):349–385. doi: 10.1177/21.4.349. [DOI] [PubMed] [Google Scholar]
- Hubbard A. L., Cohn Z. A. The enzymatic iodination of the red cell membrane. J Cell Biol. 1972 Nov;55(2):390–405. doi: 10.1083/jcb.55.2.390. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jamieson J. D., Palade G. E. Synthesis, intracellular transport, and discharge of secretory proteins in stimulated pancreatic exocrine cells. J Cell Biol. 1971 Jul;50(1):135–158. doi: 10.1083/jcb.50.1.135. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kanwar Y. S., Farquhar M. G. Anionic sites in the glomerular basement membrane. In vivo and in vitro localization to the laminae rarae by cationic probes. J Cell Biol. 1979 Apr;81(1):137–153. doi: 10.1083/jcb.81.1.137. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Meldolesi J. Dynamics of cytoplasmic membranes in guinea pig pancreatic acinar cells. I. Synthesis and turnover of membrane proteins. J Cell Biol. 1974 Apr;61(1):1–13. doi: 10.1083/jcb.61.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Novikoff A. B., Mori M., Quintana N., Yam A. Studies of the secretory process in the mammalian exocrine pancreas. I. The condensing vacuoles. J Cell Biol. 1977 Oct;75(1):148–165. doi: 10.1083/jcb.75.1.148. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Oliver C., Hand A. R. Uptake and fate of luminally administered horseradish peroxidase in resting and isoproterenol-stimulated rat parotid acinar cells. J Cell Biol. 1978 Jan;76(1):207–229. doi: 10.1083/jcb.76.1.207. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ottosen P. D., Courtoy P. J., Farquhar M. G. Pathways followed by membrane recovered from the surface of plasma cells and myeloma cells. J Exp Med. 1980 Jul 1;152(1):1–19. doi: 10.1084/jem.152.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Reddy J. K., Rao M. S. Transplantable pancreatic carcinoma of the rat. Science. 1977 Oct 7;198(4312):78–80. doi: 10.1126/science.897688. [DOI] [PubMed] [Google Scholar]
- Reddy J. K., Rao M. S., Warren J. R., Qureshi S. A., Christensen E. I. Differentiation and DNA synthesis in pancreatic acinar carcinoma of rat. Cancer Res. 1980 Oct;40(10):3443–3454. [PubMed] [Google Scholar]
- Rosenzweig L. J., Kanwar Y. S. Dopamine internalization by and intracellular distribution within prolactin cells and somatotrophs of the rat anterior pituitary as determined by quantitative electron microscopic autoradiography. Endocrinology. 1982 Dec;111(6):1817–1829. doi: 10.1210/endo-111-6-1817. [DOI] [PubMed] [Google Scholar]
- Steinman R. M., Mellman I. S., Muller W. A., Cohn Z. A. Endocytosis and the recycling of plasma membrane. J Cell Biol. 1983 Jan;96(1):1–27. doi: 10.1083/jcb.96.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Theodosis D. T., Dreifuss J., Harris M. C., Orci L. Secretion-related uptake of horseradish peroxidase in neurohypophysial axons. J Cell Biol. 1976 Aug;70(2 Pt 1):294–303. doi: 10.1083/jcb.70.2.294. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wallach D., Kirshner N., Schramm M. Non-parallel transport of membrane proteins and content proteins during assembly of the secretory granule in rat parotid gland. Biochim Biophys Acta. 1975 Jan 14;375(1):87–105. doi: 10.1016/0005-2736(75)90074-7. [DOI] [PubMed] [Google Scholar]







