Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1984 Sep 1;99(3):909–917. doi: 10.1083/jcb.99.3.909

Membrane-bound and fluid-phase macromolecules enter separate prelysosomal compartments in absorptive cells of suckling rat ileum

PMCID: PMC2113398  PMID: 6470044

Abstract

The absorptive cell of the suckling rat ileum is specialized for the uptake and digestion of milk macromolecules from the intestinal lumen. The apical cytoplasm contains an extensive tubulocisternal system, a variety of vesicles and multivesicular bodies (MVB), and a giant phagolysosomal vacuole where digestion is completed. To determine if sorting of membrane-bound and fluid-phase macromolecules occurs in this elaborate endocytic system, we infused adsorptive and soluble tracers into ligated intestinal loops in vivo and examined their fates. Lysosomal compartments were identified by acid phosphatase histochemistry. Native ferritin and two ferritin-lectin conjugates that do not bind to ileal membranes (Con A, UEAI) served as soluble tracers. Horseradish peroxidase binds to ileal membranes and thus was not useful as a fluid-phase tracer in this system. Cationized ferritin and a lectin that binds to terminal B-D-galactosyl sites on ileal membranes (Ricinus communis agglutinin [RCAI]-ferritin) were used as tracer ligands. All tracers entered the wide apical invaginations of the luminal cell surface and were transported intracellularly. Membrane- bound tracers were found in coated pits and vesicles, and throughout the tubulocisternal system (where cationized ferritin is released from the membrane) and later, in large clear vesicles and MVB. In contrast, fluid-phase tracers appeared within 5 min in vesicles of various sizes and were not transported through the tubulocisternae, rather, they were concentrated in a separate population of vesicles of increasing size that contained amorphous dense material. Large clear vesicles, large dense vesicles, and MVB eventually fused with the giant supranuclear vacuole. Acid phosphatase activity was present in MVB and in the giant vacuole but was not present in most large vesicles or in the tubulocisternae. These results demonstrate that membrane-bound and soluble protein are transported to a common lysosomal destination via separate intracellular routes involving several distinct prelysosomal compartments.

Full Text

The Full Text of this article is available as a PDF (1.5 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Abrahamson D. R., Rodewald R. Evidence for the sorting of endocytic vesicle contents during the receptor-mediated transport of IgG across the newborn rat intestine. J Cell Biol. 1981 Oct;91(1):270–280. doi: 10.1083/jcb.91.1.270. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Brown M. S., Anderson R. G., Goldstein J. L. Recycling receptors: the round-trip itinerary of migrant membrane proteins. Cell. 1983 Mar;32(3):663–667. doi: 10.1016/0092-8674(83)90052-1. [DOI] [PubMed] [Google Scholar]
  3. CLARK S. L., Jr The ingestion of proteins and colloidal materials by columnar absorptive cells of the small intestine in suckling rats and mice. J Biophys Biochem Cytol. 1959 Jan 25;5(1):41–50. doi: 10.1083/jcb.5.1.41. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Cornell R., Padykula H. A. A cytological study of intestinal absorption in the suckling rat. Am J Anat. 1969 Jul;125(3):291–315. doi: 10.1002/aja.1001250304. [DOI] [PubMed] [Google Scholar]
  5. Danon D., Goldstein L., Marikovsky Y., Skutelsky E. Use of cationized ferritin as a label of negative charges on cell surfaces. J Ultrastruct Res. 1972 Mar;38(5):500–510. doi: 10.1016/0022-5320(72)90087-1. [DOI] [PubMed] [Google Scholar]
  6. Galloway C. J., Dean G. E., Marsh M., Rudnick G., Mellman I. Acidification of macrophage and fibroblast endocytic vesicles in vitro. Proc Natl Acad Sci U S A. 1983 Jun;80(11):3334–3338. doi: 10.1073/pnas.80.11.3334. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Geuze H. J., Slot J. W., Strous G. J., Schwartz A. L. The pathway of the asialoglycoprotein-ligand during receptor-mediated endocytosis: a morphological study with colloidal gold/ligand in the human hepatoma cell line, Hep G2. Eur J Cell Biol. 1983 Nov;32(1):38–44. [PubMed] [Google Scholar]
  8. Goldstein J. L., Anderson R. G., Brown M. S. Coated pits, coated vesicles, and receptor-mediated endocytosis. Nature. 1979 Jun 21;279(5715):679–685. doi: 10.1038/279679a0. [DOI] [PubMed] [Google Scholar]
  9. 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]
  10. Gonatas N. K., Kim S. U., Stieber A., Avrameas S. Internalization of lectins in neuronal GERL. J Cell Biol. 1977 Apr;73(1):1–13. doi: 10.1083/jcb.73.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Graham R. C., Jr, Karnovsky M. J. The early stages of absorption of injected horseradish peroxidase in the proximal tubules of mouse kidney: ultrastructural cytochemistry by a new technique. J Histochem Cytochem. 1966 Apr;14(4):291–302. doi: 10.1177/14.4.291. [DOI] [PubMed] [Google Scholar]
  12. Graney D. O. The uptake of ferritin by ileal absorptive cells in suckling rats. An electron microscope study. Am J Anat. 1968 Sep;123(2):227–254. doi: 10.1002/aja.1001230202. [DOI] [PubMed] [Google Scholar]
  13. Helenius A., Marsh M. Endocytosis of enveloped animal viruses. Ciba Found Symp. 1982;(92):59–76. doi: 10.1002/9780470720745.ch4. [DOI] [PubMed] [Google Scholar]
  14. Herman B., Albertini D. F. A time-lapse video image intensification analysis of cytoplasmic organelle movements during endosome translocation. J Cell Biol. 1984 Feb;98(2):565–576. doi: 10.1083/jcb.98.2.565. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Kerjaschki D., Noronha-Blob L., Sacktor B., Farquhar M. G. Microdomains of distinctive glycoprotein composition in the kidney proximal tubule brush border. J Cell Biol. 1984 Apr;98(4):1505–1513. doi: 10.1083/jcb.98.4.1505. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Knutton S., Limbrick A. R., Robertson J. D. Regular structures in membranes. I. Membranes in the endocytic complex of ileal epithelial cells. J Cell Biol. 1974 Sep;62(3):679–694. doi: 10.1083/jcb.62.3.679. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Marsh M., Helenius A. Adsorptive endocytosis of Semliki Forest virus. J Mol Biol. 1980 Sep 25;142(3):439–454. doi: 10.1016/0022-2836(80)90281-8. [DOI] [PubMed] [Google Scholar]
  18. Maxfield F. R. Weak bases and ionophores rapidly and reversibly raise the pH of endocytic vesicles in cultured mouse fibroblasts. J Cell Biol. 1982 Nov;95(2 Pt 1):676–681. doi: 10.1083/jcb.95.2.676. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Opresko L., Wiley H. S., Wallace R. A. Differential postendocytotic compartmentation in Xenopus oocytes is mediated by a specifically bound ligand. Cell. 1980 Nov;22(1 Pt 1):47–57. doi: 10.1016/0092-8674(80)90153-1. [DOI] [PubMed] [Google Scholar]
  20. 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]
  21. Robertson J. D., Knutton S., Limbrick A. R., Jakoi E. R., Zampighi G. Regular structures in unit membranes. III. Further observations on the particulate component of the suckling rat ileum endocytic membrane complex. J Cell Biol. 1976 Jul;70(1):112–122. doi: 10.1083/jcb.70.1.112. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Rodewald R., Abrahamson D. R. Receptor-mediated transport of IgG across the intestinal epithelium of the neonatal rat. Ciba Found Symp. 1982;(92):209–232. doi: 10.1002/9780470720745.ch11. [DOI] [PubMed] [Google Scholar]
  23. Rodewald R. Distribution of immunoglobulin G receptors in the small intestine of the young rat. J Cell Biol. 1980 Apr;85(1):18–32. doi: 10.1083/jcb.85.1.18. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Shibata Y., Arima T., Arima T., Yamamoto T. Regular structures on the microvillar surface membrane of ileal epithelial cells in suckling rat intestine. J Ultrastruct Res. 1983 Oct;85(1):70–81. doi: 10.1016/s0022-5320(83)90117-x. [DOI] [PubMed] [Google Scholar]
  25. Silverstein S. C., Steinman R. M., Cohn Z. A. Endocytosis. Annu Rev Biochem. 1977;46:669–722. doi: 10.1146/annurev.bi.46.070177.003321. [DOI] [PubMed] [Google Scholar]
  26. Skutelsky E., Danon D. Redistribution of surface anionic sites on the luminal front of blood vessel endothelium after interaction with polycationic ligand. J Cell Biol. 1976 Oct;71(1):232–241. doi: 10.1083/jcb.71.1.232. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Stahl P., Schlesinger P. H., Sigardson E., Rodman J. S., Lee Y. C. Receptor-mediated pinocytosis of mannose glycoconjugates by macrophages: characterization and evidence for receptor recycling. Cell. 1980 Jan;19(1):207–215. doi: 10.1016/0092-8674(80)90402-x. [DOI] [PubMed] [Google Scholar]
  28. Staley T. E., Corley L. D., Bush L. J., Jones E. W. The ultrastructure of neonatal calf intestine and absorption of heterologous proteins. Anat Rec. 1972 Mar;172(3):559–579. doi: 10.1002/ar.1091720310. [DOI] [PubMed] [Google Scholar]
  29. Steinman R. M., Brodie S. E., Cohn Z. A. Membrane flow during pinocytosis. A stereologic analysis. J Cell Biol. 1976 Mar;68(3):665–687. doi: 10.1083/jcb.68.3.665. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. 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]
  31. Tycko B., Maxfield F. R. Rapid acidification of endocytic vesicles containing alpha 2-macroglobulin. Cell. 1982 Mar;28(3):643–651. doi: 10.1016/0092-8674(82)90219-7. [DOI] [PubMed] [Google Scholar]
  32. Walker W. A., Isselbacher K. J. Uptake and transport of macromolecules by the intestine. Possible role in clinical disorders. Gastroenterology. 1974 Sep;67(3):531–550. [PubMed] [Google Scholar]
  33. Willingham M. C., Pastan I. The receptosome: an intermediate organelle of receptor mediated endocytosis in cultured fibroblasts. Cell. 1980 Aug;21(1):67–77. doi: 10.1016/0092-8674(80)90115-4. [DOI] [PubMed] [Google Scholar]
  34. Willingham M. C., Yamada S. S. A mechanism for the destruction of pinosomes in cultured fibroblasts. Piranhalysis. J Cell Biol. 1978 Aug;78(2):480–487. doi: 10.1083/jcb.78.2.480. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Wissig S. L., Graney D. O. Membrane modifications in the apical endocytic complex of ileal epithelial cells. J Cell Biol. 1968 Dec;39(3):564–579. doi: 10.1083/jcb.39.3.564. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Worthington B. B., Graney D. O. Uptake of Adenovirus by intestinal absorptive cells of the suckling rat. I. The neonatal ileum. Anat Rec. 1973 Jan;175(1):37–61. doi: 10.1002/ar.1091750105. [DOI] [PubMed] [Google Scholar]
  37. Zeitlin P. L., Hubbard A. L. Cell surface distribution and intracellular fate of asialoglycoproteins: a morphological and biochemical study of isolated rat hepatocytes and monolayer cultures. J Cell Biol. 1982 Mar;92(3):634–647. doi: 10.1083/jcb.92.3.634. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES