Abstract
HRP has been used as a cytochemical marker for a sterelogic analysis of pinocytic vesicles and secondary lysosomes in cultivated macrophages and L cells. Evidence is presented that the diaminobenzidine technique (a) detects all vaculoes containing encyme and (b) distinguishes between incoming pinocytic vesicles and those which have fused with pre- existing lysosomes to form secondary lososomes. The HRP reactive pinocytic vesicle spaces fills completely within 5 min after exposure to enzyme, while the secondary lysosome compartment is saturated in 45-- 60 min. The size distribution of sectioned (profile) vaculoe diameters was measured at equilibrium and converted to actual (spherical) dimensions using a technique modified from Dr. S. D. Wicksell. The most important findings in this study have to do with the rate at which pinocytosed fluid and surface membrane move into the cell and on their subsequent fate. Each minute macrophages form at least 125 pinocytic vesicles having a fractional vol of 0.43% of the cell's volume and a fractional area of 3.1% of the cell's surface area. The fractional volume and surface area flux rates for L cells were 0.05% and 0.8% per minute respectively. Macrophages and L cells thus interiorize the equivalent of their cell surface area every 33 and 125 min. During a 3- period, the size of the secondary lysosome compartment remains constant and represents 2.5% of the cell volume and 18% of the surface area. Each hour, therefore, the volume and surface area of incoming vesicles is 10 times greater than the dimensions of the secondary lysosomes in both macrophages and L cells. This implies a rapid reduction in vesicle size during the formation of the secondary lysosome and the egress of pinocytosed fluid from the vacuole and the cell. In addition, we postulate that membrane components of the vacuole are subsequently recycled back to the cell surface.
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- Abrahams S. J., Holtzman E. Secretion and endocytosis in insulin-stimulated rat adrenal medulla cells. J Cell Biol. 1973 Feb;56(2):540–558. doi: 10.1083/jcb.56.2.540. [DOI] [PMC free article] [PubMed] [Google Scholar]
- COHN Z. A., BENSON B. THE DIFFERENTIATION OF MONONUCLEAR PHAGOCYTES. MORPHOLOGY, CYTOCHEMISTRY, AND BIOCHEMISTRY. J Exp Med. 1965 Jan 1;121:153–170. doi: 10.1084/jem.121.1.153. [DOI] [PMC free article] [PubMed] [Google Scholar]
- CURRAN P. F., MACINTOSH J. R. A model system for biological water transport. Nature. 1962 Jan 27;193:347–348. doi: 10.1038/193347a0. [DOI] [PubMed] [Google Scholar]
- Ceccarelli B., Hurlbut W. P., Mauro A. Depletion of vesicles from frog neuromuscular junctions by prolonged tetanic stimulation. J Cell Biol. 1972 Jul;54(1):30–38. doi: 10.1083/jcb.54.1.30. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cohn Z. A., Benson B. The in vitro differentiation of mononuclear phagocytes. 3. The reversibility of granule and hydrolytic enzyme formation and the turnover of granule constituents. J Exp Med. 1965 Sep 1;122(3):455–466. doi: 10.1084/jem.122.3.455. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cohn Z. A., Ehrenreich B. A. The uptake, storage, and intracellular hydrolysis of carbohydrates by macrophages. J Exp Med. 1969 Jan 1;129(1):201–225. doi: 10.1084/jem.129.1.201. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cohn Z. A., Fedorko M. E., Hirsch J. G. The in vitro differentiation of mononuclear phagocytes. V. The formation of macrophage lysosomes. J Exp Med. 1966 Apr 1;123(4):757–766. doi: 10.1084/jem.123.4.757. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DIAMOND J. M. THE MECHANISM OF ISOTONIC WATER TRANSPORT. J Gen Physiol. 1964 Sep;48:15–42. doi: 10.1085/jgp.48.1.15. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ELIAS H. Contributions to the geometry of sectioning. III. Spheres in masses. Z Wiss Mikrosk. 1954 Oct;62(1):32–40. [PubMed] [Google Scholar]
- Edelson P. J., Cohn Z. A. Effects of concanavalin A on mouse peritoneal macrophages. I. Stimulation of endocytic activity and inhibition of phago-lysosome formation. J Exp Med. 1974 Nov 1;140(5):1364–1386. doi: 10.1084/jem.140.5.1364. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ehrenreich B. A., Cohn Z. A. Fate of hemoglobin pincytosed by macrophages in vitro. J Cell Biol. 1968 Jul;38(1):244–248. doi: 10.1083/jcb.38.1.244. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ehrenreich B. A., Cohn Z. A. The fate of peptides pinocytosed by macrophages in vitro. J Exp Med. 1969 Jan 1;129(1):227–245. doi: 10.1084/jem.129.1.227. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ehrenreich B. A., Cohn Z. A. The uptake and digestion of iodinated human serum albumin by macrophages in vitro. J Exp Med. 1967 Nov 1;126(5):941–958. doi: 10.1084/jem.126.5.941. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Elias H., Hennig A., Schwartz D. E. Stereology: applications to biomedicalresearch. Physiol Rev. 1971 Jan;51(1):158–200. doi: 10.1152/physrev.1971.51.1.158. [DOI] [PubMed] [Google Scholar]
- Franke W. W., Herth W. Morphological evidence for de novo formation of plasma membrane from coated vesicles in exponentially growing cultured plant cells. Exp Cell Res. 1974 Dec;89(2):447–451. doi: 10.1016/0014-4827(74)90821-0. [DOI] [PubMed] [Google Scholar]
- Friend D. S., Farquhar M. G. Functions of coated vesicles during protein absorption in the rat vas deferens. J Cell Biol. 1967 Nov;35(2):357–376. doi: 10.1083/jcb.35.2.357. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gordon S., Todd J., Cohn Z. A. In vitro synthesis and secretion of lysozyme by mononuclear phagocytes. J Exp Med. 1974 May 1;139(5):1228–1248. doi: 10.1084/jem.139.5.1228. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Henning R., Kaulen H. D., Stoffel W. Biochemical analysis of the pinocytotic process. I. Isolation and chemical composition of the lysosomal and the plasma membrane of the rat liver cell. Hoppe Seylers Z Physiol Chem. 1970 Oct;351(10):1191–1199. doi: 10.1515/bchm2.1970.351.2.1191. [DOI] [PubMed] [Google Scholar]
- Henning R., Stoffel W. Glycosphingolipids in lysosomal membranes. Hoppe Seylers Z Physiol Chem. 1973 Jul;354(7):760–770. doi: 10.1515/bchm2.1973.354.2.760. [DOI] [PubMed] [Google Scholar]
- Heuser J. E., Reese T. S. Evidence for recycling of synaptic vesicle membrane during transmitter release at the frog neuromuscular junction. J Cell Biol. 1973 May;57(2):315–344. doi: 10.1083/jcb.57.2.315. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hirsch J. G., Fedorko M. E., Cohn Z. A. Vesicle fusion and formation at the surface of pinocytic vacuoles in macrophages. J Cell Biol. 1968 Sep;38(3):629–632. doi: 10.1083/jcb.38.3.629. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hirsch J. G., Fedorko M. E. Ultrastructure of human leukocytes after simultaneous fixation with glutaraldehyde and osmium tetroxide and "postfixation" in uranyl acetate. J Cell Biol. 1968 Sep;38(3):615–627. doi: 10.1083/jcb.38.3.615. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hubbard A. L., Cohn Z. A. Externally disposed plasma membrane proteins. II. Metabolic fate of iodinated polypeptides of mouse L cells. J Cell Biol. 1975 Feb;64(2):461–479. doi: 10.1083/jcb.64.2.461. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kaulen H. D., Henning R., Stoffel W. Biochemical analsis of the inocytotic process. II. Comparison of some enzymes of the lysosomal nd the plasma membrane of the rat liver cel. Hoppe Seylers Z Physiol Chem. 1970 Dec;351(12):1555–1563. doi: 10.1515/bchm2.1970.351.2.1555. [DOI] [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- Loud A. V. A quantitative stereological description of the ultrastructure of normal rat liver parenchymal cells. J Cell Biol. 1968 Apr;37(1):27–46. doi: 10.1083/jcb.37.1.27. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Orci L., Malaisse-Lagae F., Ravazzola M., Amherdt M., Renold A. E. Exocytosis-endocytosis coupling in the pancreatic beta cell. Science. 1973 Aug 10;181(4099):561–562. doi: 10.1126/science.181.4099.561. [DOI] [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]
- Schulman J. D., Bradley K. H. The metabolism of amino acids, peptides, and disulfides in lysosomes of fibroblasts cultured from normal individuals and those with cystinosis. J Exp Med. 1970 Dec 1;132(6):1090–1104. doi: 10.1084/jem.132.6.1090. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sheffield J. B. Studies on aggregation of embryonic cells: initial cell adhesions and the formation of intercellular junctions. J Morphol. 1970 Nov;132(3):245–263. doi: 10.1002/jmor.1051320302. [DOI] [PubMed] [Google Scholar]
- Steinman R. M., Cohn Z. A. The interaction of soluble horseradish peroxidase with mouse peritoneal macrophages in vitro. J Cell Biol. 1972 Oct;55(1):186–204. doi: 10.1083/jcb.55.1.186. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Steinman R. M., Silver J. M., Cohn Z. A. Pinocytosis in fibroblasts. Quantitative studies in vitro. J Cell Biol. 1974 Dec;63(3):949–969. doi: 10.1083/jcb.63.3.949. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tartakoff A., Greene L. J., Palade G. E. Studies on the guinea pig pancreas. Fractionation and partial characterization of exocrine proteins. J Biol Chem. 1974 Dec 10;249(23):7420–7431. [PubMed] [Google Scholar]
- Tsan M. F., Berlin R. D. Effect of phagocytosis on membrane transport of nonelectrolytes. J Exp Med. 1971 Oct 1;134(4):1016–1035. doi: 10.1084/jem.134.4.1016. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Unkeless J. C., Gordon S., Reich E. Secretion of plasminogen activator by stimulated macrophages. J Exp Med. 1974 Apr 1;139(4):834–850. doi: 10.1084/jem.139.4.834. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wagner R., Rosenberg M., Estensen R. Endocytosis in Chang liver cells. Quantitation by sucrose- 3 H uptake and inhibition by cytochalasin B. J Cell Biol. 1971 Sep;50(3):804–817. doi: 10.1083/jcb.50.3.804. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Warren L., Glick M. C. Membranes of animal cells. II. The metabolism and turnover of the surface membrane. J Cell Biol. 1968 Jun;37(3):729–746. doi: 10.1083/jcb.37.3.729. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Werb Z., Cohn Z. A. Cholesterol metabolism in the macrophage. II. Alteration of subcellular exchangeable cholesterol compartments and exchange in other cell types. J Exp Med. 1971 Dec 1;134(6):1570–1590. doi: 10.1084/jem.134.6.1570. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Werb Z., Cohn Z. A. Plasma membrane synthesis in the macrophage following phagocytosis of polystyrene latex particles. J Biol Chem. 1972 Apr 25;247(8):2439–2446. [PubMed] [Google Scholar]
- Wills E. J., Davies P., Allison A. C., Haswell A. D. Cytochalasin B fails to inhibit pinocytosis by macrophages. Nat New Biol. 1972 Nov 8;240(97):58–60. doi: 10.1038/newbio240058a0. [DOI] [PubMed] [Google Scholar]
- von Figura K., Kresse H. Quantitative aspects of pinocytosis and the intracellular fate of N-acetyl-alpha-D-glucosaminidase in Sanfilippo B fibroblasts. J Clin Invest. 1974 Jan;53(1):85–90. doi: 10.1172/JCI107563. [DOI] [PMC free article] [PubMed] [Google Scholar]