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. 1990 Nov 1;111(5):1811–1823. doi: 10.1083/jcb.111.5.1811

Isolation and preliminary characterization of the major membrane boundaries of the endocytic pathway in lymphocytes

PMCID: PMC2116323  PMID: 2121741

Abstract

Plasma membrane, coated pits, endosomes, and lysosomes were isolated from a mouse T lymphoma cell line using a density shift protocol in which these compartments were selectively loaded with gold conjugates. The plasma membrane was prepared after selective labeling for 1 h at 2 degrees C with gold-ricin and gave a yield of 40% according to enzymatic and antigenic markers. Endosomes were obtained by loading the cells for 2 h at 22 degrees C with gold complexed to an antimouse transferrin receptor mAb. Coated pits were isolated using a similar procedure, but after an incubation at 10 degrees C, which allowed deep invagination of the pits but prevented internalization. The yield (calculated using the recovery of [125I]transferrin) was 32% for endosomes and 10% for coated pits. Finally lysosomes were prepared by loading the cells for 18 h at 37 degrees C with gold low density lipoproteins (LDLs) followed by a 3-h chase at 37 degrees C with LDL alone. The final lysosome yield (based on the recovery of lysosomal enzymes) was 16%. Studies of the protein composition of these cellular compartments on two-dimensional gels showed that while some major proteins are present throughout the pathway, specific proteins can be identified in each of the isolated fractions. The greatest change in the pattern of protein constituents seen along the pathway was between endosomal and lysosomal preparations.

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Selected References

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  1. Adamski J., Sierralta W. D., Jungblut P. W. Harvesting and separation of two populations of lysosomes from porcine endometrium. Eur J Cell Biol. 1988 Feb;45(2):238–245. [PubMed] [Google Scholar]
  2. Ajioka R. S., Kaplan J. Intracellular pools of transferrin receptors result from constitutive internalization of unoccupied receptors. Proc Natl Acad Sci U S A. 1986 Sep;83(17):6445–6449. doi: 10.1073/pnas.83.17.6445. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Allan D., Crumpton M. J. Preparation and characterization of the plasma membrane of pig lymphocytes. Biochem J. 1970 Nov;120(1):133–143. doi: 10.1042/bj1200133. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Ames G. F., Nikaido K. Two-dimensional gel electrophoresis of membrane proteins. Biochemistry. 1976 Feb 10;15(3):616–623. doi: 10.1021/bi00648a026. [DOI] [PubMed] [Google Scholar]
  5. Beardmore J., Howell K. E., Miller K., Hopkins C. R. Isolation of an endocytic compartment from A431 cells using a density modification procedure employing a receptor-specific monoclonal antibody complexed with colloidal gold. J Cell Sci. 1987 May;87(Pt 4):495–506. doi: 10.1242/jcs.87.4.495. [DOI] [PubMed] [Google Scholar]
  6. Beaumelle B. D., Hopkins C. R. High-yield isolation of functionally competent endosomes from mouse lymphocytes. Biochem J. 1989 Nov 15;264(1):137–149. doi: 10.1042/bj2640137. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Benhamou N., Ouellette G. B. Ultrastructural localization of glycoconjugates in the fungus Ascocalyx abietina, the Scleroderris canker agent of conifers, using lectin-gold complexes. J Histochem Cytochem. 1986 Jul;34(7):855–867. doi: 10.1177/34.7.3519750. [DOI] [PubMed] [Google Scholar]
  8. Bourguignon L. Y., Suchard S. J., Nagpal M. L., Glenney J. R., Jr A T-lymphoma transmembrane glycoprotein (gp180) is linked to the cytoskeletal protein, fodrin. J Cell Biol. 1985 Aug;101(2):477–487. doi: 10.1083/jcb.101.2.477. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Brodsky F. M. Living with clathrin: its role in intracellular membrane traffic. Science. 1988 Dec 9;242(4884):1396–1402. doi: 10.1126/science.2904698. [DOI] [PubMed] [Google Scholar]
  10. Carlsson S. R., Roth J., Piller F., Fukuda M. Isolation and characterization of human lysosomal membrane glycoproteins, h-lamp-1 and h-lamp-2. Major sialoglycoproteins carrying polylactosaminoglycan. J Biol Chem. 1988 Dec 15;263(35):18911–18919. [PubMed] [Google Scholar]
  11. Carriere D., Arcier J. M., Derocq J. M., Fontaine C., Richer G. Antigenic modulation induced by four monoclonal antibodies adsorbed on gold particles (specificity anti-CD4, anti-CD5, anti-CD7, and anti-150-kDa antigen): relationship between modulation and cytotoxic activity of immunotoxins. Exp Cell Res. 1989 May;182(1):114–128. doi: 10.1016/0014-4827(89)90284-x. [DOI] [PubMed] [Google Scholar]
  12. Corte G., Calabi F., Damiani G., Bargellesi A., Tosi R., Sorrentino R. Human Ia molecules carrying DC1 determinants differ in both alpha- and beta-subunits from Ia molecules carrying DR determinants. Nature. 1981 Jul 23;292(5821):357–360. doi: 10.1038/292357a0. [DOI] [PubMed] [Google Scholar]
  13. Courtoy P. J., Quintart J., Baudhuin P. Shift of equilibrium density induced by 3,3'-diaminobenzidine cytochemistry: a new procedure for the analysis and purification of peroxidase-containing organelles. J Cell Biol. 1984 Mar;98(3):870–876. doi: 10.1083/jcb.98.3.870. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Daiss J. L., Roth T. F. Isolation of coated vesicles: comparative studies. Methods Enzymol. 1983;98:337–349. doi: 10.1016/0076-6879(83)98162-4. [DOI] [PubMed] [Google Scholar]
  15. Devaney E., Howell K. E. Immuno-isolation of a plasma membrane fraction from the Fao cell. EMBO J. 1985 Dec 1;4(12):3123–3130. doi: 10.1002/j.1460-2075.1985.tb04054.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Dickson R. B., Beguinot L., Hanover J. A., Richert N. D., Willingham M. C., Pastan I. Isolation and characterization of a highly enriched preparation of receptosomes (endosomes) from a human cell line. Proc Natl Acad Sci U S A. 1983 Sep;80(17):5335–5339. doi: 10.1073/pnas.80.17.5335. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Draye J. P., Courtoy P. J., Quintart J., Baudhuin P. Relations between plasma membrane and lysosomal membrane. 2. Quantitative evaluation of plasma membrane marker enzymes in the lysosomes. Eur J Biochem. 1987 Dec 30;170(1-2):405–411. doi: 10.1111/j.1432-1033.1987.tb13714.x. [DOI] [PubMed] [Google Scholar]
  18. Draye J. P., Quintart J., Courtoy P. J., Baudhuin P. Relations between plasma membrane and lysosomal membrane. 1. Fate of covalently labelled plasma membrane protein. Eur J Biochem. 1987 Dec 30;170(1-2):395–403. doi: 10.1111/j.1432-1033.1987.tb13713.x. [DOI] [PubMed] [Google Scholar]
  19. Enrich C., Bachs O., Evans W. H. A 115 kDa calmodulin-binding protein is located in rat liver endosome fractions. Biochem J. 1988 Nov 1;255(3):999–1005. doi: 10.1042/bj2550999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Ferber E., Resch K., Wallach D. F., Imm W. Isolation and characterization of lymphocyte plasma membranes. Biochim Biophys Acta. 1972 May 9;266(2):494–504. doi: 10.1016/0005-2736(72)90105-8. [DOI] [PubMed] [Google Scholar]
  21. GREENWOOD F. C., HUNTER W. M., GLOVER J. S. THE PREPARATION OF I-131-LABELLED HUMAN GROWTH HORMONE OF HIGH SPECIFIC RADIOACTIVITY. Biochem J. 1963 Oct;89:114–123. doi: 10.1042/bj0890114. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Geoghegan W. D., Ackerman G. A. Adsorption of horseradish peroxidase, ovomucoid and anti-immunoglobulin to colloidal gold for the indirect detection of concanavalin A, wheat germ agglutinin and goat anti-human immunoglobulin G on cell surfaces at the electron microscopic level: a new method, theory and application. J Histochem Cytochem. 1977 Nov;25(11):1187–1200. doi: 10.1177/25.11.21217. [DOI] [PubMed] [Google Scholar]
  23. Goldberg D. E., Kornfeld S. Evidence for extensive subcellular organization of asparagine-linked oligosaccharide processing and lysosomal enzyme phosphorylation. J Biol Chem. 1983 Mar 10;258(5):3159–3165. [PubMed] [Google Scholar]
  24. Griffiths G., Hoflack B., Simons K., Mellman I., Kornfeld S. The mannose 6-phosphate receptor and the biogenesis of lysosomes. Cell. 1988 Feb 12;52(3):329–341. doi: 10.1016/s0092-8674(88)80026-6. [DOI] [PubMed] [Google Scholar]
  25. Gruenberg J. E., Howell K. E. Reconstitution of vesicle fusions occurring in endocytosis with a cell-free system. EMBO J. 1986 Dec 1;5(12):3091–3101. doi: 10.1002/j.1460-2075.1986.tb04615.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Gupta D. K., Tartakoff A. M. A novel lectin-gold density perturbation eliminates plasma membrane contaminants from Golgi-enriched subcellular fractions. Eur J Cell Biol. 1989 Feb;48(1):64–70. [PubMed] [Google Scholar]
  27. HAVEL R. J., EDER H. A., BRAGDON J. H. The distribution and chemical composition of ultracentrifugally separated lipoproteins in human serum. J Clin Invest. 1955 Sep;34(9):1345–1353. doi: 10.1172/JCI103182. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Handley D. A., Arbeeny C. M., Witte L. D., Chien S. Colloidal gold--low density lipoprotein conjugates as membrane receptor probes. Proc Natl Acad Sci U S A. 1981 Jan;78(1):368–371. doi: 10.1073/pnas.78.1.368. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Harms E., Kartenbeck J., Darai G., Schneider J. Purification and characterization of human lysosomes from EB-virus transformed lymphoblasts. Exp Cell Res. 1981 Feb;131(2):251–266. doi: 10.1016/0014-4827(81)90230-5. [DOI] [PubMed] [Google Scholar]
  30. Hartree E. F. Determination of protein: a modification of the Lowry method that gives a linear photometric response. Anal Biochem. 1972 Aug;48(2):422–427. doi: 10.1016/0003-2697(72)90094-2. [DOI] [PubMed] [Google Scholar]
  31. Helmy S., Porter-Jordan K., Dawidowicz E. A., Pilch P., Schwartz A. L., Fine R. E. Separation of endocytic from exocytic coated vesicles using a novel cholinesterase mediated density shift technique. Cell. 1986 Feb 14;44(3):497–506. doi: 10.1016/0092-8674(86)90471-x. [DOI] [PubMed] [Google Scholar]
  32. Heuser J. Changes in lysosome shape and distribution correlated with changes in cytoplasmic pH. J Cell Biol. 1989 Mar;108(3):855–864. doi: 10.1083/jcb.108.3.855. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Hopkins C. R. Intracellular routing of transferrin and transferrin receptors in epidermoid carcinoma A431 cells. Cell. 1983 Nov;35(1):321–330. doi: 10.1016/0092-8674(83)90235-0. [DOI] [PubMed] [Google Scholar]
  34. Johnson G. L., Bourne H. R. Influence of cholera toxin on the regulation of adenylate cyclase by GTP. Biochem Biophys Res Commun. 1977 Sep 23;78(2):792–798. doi: 10.1016/0006-291x(77)90249-2. [DOI] [PubMed] [Google Scholar]
  35. Khan M. N., Savoie S., Bergeron J. J., Posner B. I. Characterization of rat liver endosomal fractions. In vivo activation of insulin-stimulable receptor kinase in these structures. J Biol Chem. 1986 Jun 25;261(18):8462–8472. [PubMed] [Google Scholar]
  36. 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]
  37. Lesley J., Domingo D. L., Schulte R., Trowbridge I. S. Effect of an anti-murine transferrin receptor-ricin A conjugate on bone marrow stem and progenitor cells treated in vitro. Exp Cell Res. 1984 Feb;150(2):400–407. doi: 10.1016/0014-4827(84)90583-4. [DOI] [PubMed] [Google Scholar]
  38. Marsh M., Schmid S., Kern H., Harms E., Male P., Mellman I., Helenius A. Rapid analytical and preparative isolation of functional endosomes by free flow electrophoresis. J Cell Biol. 1987 Apr;104(4):875–886. doi: 10.1083/jcb.104.4.875. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Merion M., Sly W. S. The role of intermediate vesicles in the adsorptive endocytosis and transport of ligand to lysosomes by human fibroblasts. J Cell Biol. 1983 Mar;96(3):644–650. doi: 10.1083/jcb.96.3.644. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Merisko E. M., Farquhar M. G., Palade G. E. Coated vesicle isolation by immunoadsorption on Staphylococcus aureus cells. J Cell Biol. 1982 Mar;92(3):846–857. doi: 10.1083/jcb.92.3.846. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Mersel M., Lelong I., Hindelang C., Sarlieve L., Vincendon G. Isolation of plasma membranes from neurons grown in primary culture. Anal Biochem. 1987 Nov 1;166(2):246–252. doi: 10.1016/0003-2697(87)90571-9. [DOI] [PubMed] [Google Scholar]
  42. O'Farrell P. H. High resolution two-dimensional electrophoresis of proteins. J Biol Chem. 1975 May 25;250(10):4007–4021. [PMC free article] [PubMed] [Google Scholar]
  43. O'Farrell P. Z., Goodman H. M., O'Farrell P. H. High resolution two-dimensional electrophoresis of basic as well as acidic proteins. Cell. 1977 Dec;12(4):1133–1141. doi: 10.1016/0092-8674(77)90176-3. [DOI] [PubMed] [Google Scholar]
  44. Omary M. B., Trowbridge I. S. Disposition of T200 glycoprotein in the plasma membrane of a murine lymphoma cell line. J Biol Chem. 1980 Feb 25;255(4):1662–1669. [PubMed] [Google Scholar]
  45. Pastan I., Willingham M. C., FitzGerald D. J. Immunotoxins. Cell. 1986 Dec 5;47(5):641–648. doi: 10.1016/0092-8674(86)90506-4. [DOI] [PubMed] [Google Scholar]
  46. Pearse B. M. Receptors compete for adaptors found in plasma membrane coated pits. EMBO J. 1988 Nov;7(11):3331–3336. doi: 10.1002/j.1460-2075.1988.tb03204.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Sahagian G. G., Neufeld E. F. Biosynthesis and turnover of the mannose 6-phosphate receptor in cultured Chinese hamster ovary cells. J Biol Chem. 1983 Jun 10;258(11):7121–7128. [PubMed] [Google Scholar]
  48. Schmid S. L., Fuchs R., Male P., Mellman I. Two distinct subpopulations of endosomes involved in membrane recycling and transport to lysosomes. Cell. 1988 Jan 15;52(1):73–83. doi: 10.1016/0092-8674(88)90532-6. [DOI] [PubMed] [Google Scholar]
  49. Shibata Y., Abiko Y., Arii H., Sone M., Takiguchi H. Rapid procedure for preparation of macrophage plasma membrane. Int J Biochem. 1987;19(6):489–493. doi: 10.1016/0020-711x(87)90131-5. [DOI] [PubMed] [Google Scholar]
  50. Simmons B. M., Stahl P. D., Russell J. H. Mannose receptor-mediated uptake of ricin toxin and ricin A chain by macrophages. Multiple intracellular pathways for a chain translocation. J Biol Chem. 1986 Jun 15;261(17):7912–7920. [PubMed] [Google Scholar]
  51. Slot J. W., Geuze H. J. A new method of preparing gold probes for multiple-labeling cytochemistry. Eur J Cell Biol. 1985 Jul;38(1):87–93. [PubMed] [Google Scholar]
  52. Till M. A., Zolla-Pazner S., Gorny M. K., Patton J. S., Uhr J. W., Vitetta E. S. Human immunodeficiency virus-infected T cells and monocytes are killed by monoclonal human anti-gp41 antibodies coupled to ricin A chain. Proc Natl Acad Sci U S A. 1989 Mar;86(6):1987–1991. doi: 10.1073/pnas.86.6.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Watts C., Davidson H. W. Endocytosis and recycling of specific antigen by human B cell lines. EMBO J. 1988 Jul;7(7):1937–1945. doi: 10.1002/j.1460-2075.1988.tb03031.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Wileman T., Harding C., Stahl P. Receptor-mediated endocytosis. Biochem J. 1985 Nov 15;232(1):1–14. doi: 10.1042/bj2320001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. van Deurs B., Pedersen L. R., Sundan A., Olsnes S., Sandvig K. Receptor-mediated endocytosis of a ricin-colloidal gold conjugate in vero cells. Intracellular routing to vacuolar and tubulo-vesicular portions of the endosomal system. Exp Cell Res. 1985 Aug;159(2):287–304. doi: 10.1016/s0014-4827(85)80003-3. [DOI] [PubMed] [Google Scholar]
  56. van Deurs B., Petersen O. W., Olsnes S., Sandvig K. The ways of endocytosis. Int Rev Cytol. 1989;117:131–177. doi: 10.1016/s0074-7696(08)61336-4. [DOI] [PubMed] [Google Scholar]
  57. van den Bosch R. A., du Maine A. P., Geuze H. J., van der Ende A., Strous G. J. Recycling of 5'-nucleotidase in a rat hepatoma cell line. EMBO J. 1988 Nov;7(11):3345–3351. doi: 10.1002/j.1460-2075.1988.tb03206.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. von Figura K., Hasilik A. Lysosomal enzymes and their receptors. Annu Rev Biochem. 1986;55:167–193. doi: 10.1146/annurev.bi.55.070186.001123. [DOI] [PubMed] [Google Scholar]

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