Multivesicular bodies isolated from rat hepatocytes. Cytochemical evidence for transformation into secondary lysosomes by fusion with primary lysosomes - PubMed (original) (raw)
- PMID: 2430918
- DOI: 10.1007/BF00508427
Multivesicular bodies isolated from rat hepatocytes. Cytochemical evidence for transformation into secondary lysosomes by fusion with primary lysosomes
E Jost-Vu et al. Histochemistry. 1986.
Abstract
Plasma lipoproteins (and other ligands) are endocytosed by hepatocytes and appear in multivesicular bodies (MVBs) in the Golgi-lysosome region of the cell prior to their degradation. We have isolated MVB fractions from livers of estradiol-treated rats, permitting studies of their properties (Hornick et al. 1985). Here we report our cytochemical studies of lysosomal enzyme activity in partially and highly purified MVB fractions and in MVBs in hepatocytes in situ. Only about 15% of partially or highly purified MVBs were positive for acid phosphatase and arylsulfatase, consistent with the prelysosomal nature of this compartment. Partially purified MVB fractions contained small round vesicles, 70-120 nm in diameter, which stained intensely for these enzymes; occasionally these vesicles appeared to fuse with MVBs, suggesting that these structures are primary lysosomes. Such stained vesicles were rarely seen in highly purified MVB preparations. Acid phosphatase reaction product with cerium as capture reagent appeared as uniform precipitates surrounding endocytosed plasma lipoproteins in positively stained MVBs. Arylsulfatase reaction product, however, appeared as distinctive arc or plaque-like deposits just inside the MVB-limiting membrane, often in continuity with intense reaction product contained in a fusing primary lysosome. Similar putative primary lysosomes were occasionally observed in isolated, "intact" Golgi fractions from the same livers. Similar histochemical reactivities of MVBs and putative primary lysosomes were observed in thin sections of hepatocytes in situ. These observations support the conclusion that, in hepatocytes, MVBs represent the immediate prelysosomal compartment in the endocytic pathway of macromolecular catabolism, and suggest that MVBs are converted to secondary lysosomes by direct fusion with primary lysosomes arising from closely adjacent Golgi compartments.
Similar articles
- Isolation and characterization of multivesicular bodies from rat hepatocytes: an organelle distinct from secretory vesicles of the Golgi apparatus.
Hornick CA, Hamilton RL, Spaziani E, Enders GH, Havel RJ. Hornick CA, et al. J Cell Biol. 1985 May;100(5):1558-69. doi: 10.1083/jcb.100.5.1558. J Cell Biol. 1985. PMID: 3988801 Free PMC article. - Cytochemical staining of multivesicular body and golgi vesicles.
Friend DS. Friend DS. J Cell Biol. 1969 Apr;41(1):269-79. doi: 10.1083/jcb.41.1.269. J Cell Biol. 1969. PMID: 4180353 Free PMC article. - Ultrastructural localization of lysosomal enzymes in the egg cortex of Brachydanio.
Hart NH, Wolenski JS, Donovan MJ. Hart NH, et al. J Exp Zool. 1987 Oct;244(1):17-32. doi: 10.1002/jez.1402440104. J Exp Zool. 1987. PMID: 2826641 - Hepatocytic lipoprotein receptors and intracellular lipoprotein catabolism.
Havel RJ, Hamilton RL. Havel RJ, et al. Hepatology. 1988 Nov-Dec;8(6):1689-704. doi: 10.1002/hep.1840080637. Hepatology. 1988. PMID: 2847970 Review. - Biogenesis of lysosomes by endocytic flow of plasma membrane.
Morales CR, Zhao Q, Lefrancois S. Morales CR, et al. Biocell. 1999 Dec;23(3):149-60. Biocell. 1999. PMID: 10904540 Review.
Cited by
- Isolation and characterization of three endosomal fractions from the liver of estradiol-treated rats.
Belcher JD, Hamilton RL, Brady SE, Hornick CA, Jaeckle S, Schneider WJ, Havel RJ. Belcher JD, et al. Proc Natl Acad Sci U S A. 1987 Oct;84(19):6785-9. doi: 10.1073/pnas.84.19.6785. Proc Natl Acad Sci U S A. 1987. PMID: 3477810 Free PMC article. - Effect of colchicine on lysosomal structures in maturation-ameloblasts of the rat incisor.
Salama AH, Eisenmann DR, Zaki AE. Salama AH, et al. Cell Tissue Res. 1990 May;260(3):565-73. doi: 10.1007/BF00297237. Cell Tissue Res. 1990. PMID: 2164885 - Identification and distribution of proteins in isolated endosomal fractions of rat liver: involvement in endocytosis, recycling and transcytosis.
Pol A, Ortega D, Enrich C. Pol A, et al. Biochem J. 1997 Apr 15;323 ( Pt 2)(Pt 2):435-43. doi: 10.1042/bj3230435. Biochem J. 1997. PMID: 9163335 Free PMC article. - The cytoplasmic domain mediates localization of furin to the trans-Golgi network en route to the endosomal/lysosomal system.
Bosshart H, Humphrey J, Deignan E, Davidson J, Drazba J, Yuan L, Oorschot V, Peters PJ, Bonifacino JS. Bosshart H, et al. J Cell Biol. 1994 Sep;126(5):1157-72. doi: 10.1083/jcb.126.5.1157. J Cell Biol. 1994. PMID: 7914893 Free PMC article.
References
- J Cell Biol. 1971 Aug;50(2):498-515 - PubMed
- J Cell Biol. 1985 Apr;100(4):1235-47 - PubMed
- J Cell Biol. 1981 Dec;91(3 Pt 2):66s-76s - PubMed
- J Histochem Cytochem. 1977 Dec;25(12 ):1381-4 - PubMed
- J Biol Chem. 1979 Nov 25;254(22):11367-73 - PubMed