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Chicken oocyte growth: receptor-mediated yolk deposition

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Abstract

During the rapid final stage of growth, chicken oocytes take up massive amounts of plasma components and convert them to yolk. The oocyte expresses a receptor that binds both major yolk lipoprotein precursors, vitellogenin (VTG) and very low density lipoprotein (VLDL). In the present study, in vivo transport tracing methodology, isolation of coated vesicles, ligand- and immuno-blotting, and ultrastructural immunocytochemistry were used for the analysis of receptor-mediated yolk formation. The VTG/VLDL receptor was identified in coated profiles in the oocyte periphery, in isolated coated vesicles, and within vesicular compartments both outside and inside membrane-bounded yolk storage organelles (yolk spheres). VLDL particles colocalized with the receptor, as demonstrated by ultrastructural visualization of VLDL-gold following intravenous administration, as well as by immunocytochemical analysis with antibodies to VLDL. Lipoprotein particles were shown to reach the oocyte surface by passage across the basement membrane, which possibly plays an active and selective role in yolk precursor accessibility to the oocyte surface, and through gaps between the follicular granulosa cells. Following delivery of ligands from the plasma membrane into yolk spheres, proteolytic processing of VTG and VLDL by cathepsin D appears to correlate with segregation of receptors and ligands which enter disparate sub-compartments within the yolk spheres. In small, quiescent oocytes, the VTG/VLDL receptor was localized to the central portion of the cell. At onset of the rapid growth phase, it appears that this pre-existing pool of receptors redistributes to the peripheral region, thereby initiating yolk formation. Such a redistribution mechanism would obliterate the need for de novo synthesis of receptors when the oocyte's energy expenditure is to be utilized for plasma membrane synthesis, establishment and maintenance of intracellular topography and yolk formation, and preparation for ovulation.

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References

  • Barakat HA, St Clair R (1985) Characterization of plasma lipoproteins of grain- and cholesterol-fed White Carneau and Show Racer pigeons. J Lipid Res 26:1252–1268

    Google Scholar 

  • Barber DL, Sanders EJ, Aebersold R, Schneider WJ (1991) The receptor for yolk lipoprotein deposition in the chicken oocyte. J Biol Chem 266:18761–18770

    Google Scholar 

  • Beisiegel U, Schneider WJ, Goldstein JL, Anderson RGW, Brown MS (1981) Monoclonal antibodies to the LDL receptor as probes for study of receptor-mediated endocytosis and the genetics of familial hypercholesterolemia. J Biol Chem 256:11923–11931

    Google Scholar 

  • Bellairs R, Backhouse M, Evans RJ (1972) A correlated chemical and morphological study of egg yolk and its constituents. Micron 3:328–346

    Google Scholar 

  • Bendayan M, Stephens N (1984) Double labelling cytochemistry applying the protein A-gold technique. In: Polak JM, Varndell IM (eds) Immunolabelling for electron microscopy. Elsevier, Amsterdam, pp 143–154

    Google Scholar 

  • Brown MS, Goldstein JL (1986) A receptor-mediated pathway for cholesterol homeostasis. Science 232:34–47

    Google Scholar 

  • Camejo G, Rosengren B, Olson U, Lopez F, Olofson S-O, Westerlund C, Bondjers G (1990) Molecular basis of the association of arterial proteoglycans with low density lipoproteins: its effect on the structures of the lipoprotein particle. Eur Heart J 11 [Suppl E]:164–173

    Google Scholar 

  • Davidson EH (1986) Gene activity in early development. Academic Press, London, pp 1–670

    Google Scholar 

  • Deeley RG, Mullinix KP, Wetekam K, Kronenberg HM, Meyers M, Eldridge JD, Goldberger RF (1975) Vitellogenin synthesis in the avian liver Vitellogenin is the precursor of the egg yolk phosphoproteins. J Biol Chem 250:9060–9066

    Google Scholar 

  • Dumont JN (1978) Oogenesis in Xenopus laevis (Daudin). VI. The route of injected tracer transport in the follicle and developing oocyte. J Exp Zool 204:193–218

    Google Scholar 

  • Evans AJ, Perry MM, Gilbert AB (1979) The demonstration of very low density lipoprotein in the basal lamina of the granulosa layer in the hen's ovarian follicle. Biochim Biophys Acta 573:184–195

    Google Scholar 

  • Fraker PJ, Speck JC (1978) Protein and cell membrane iodinations with a sparingly soluble chloroamide, 1.3.4.6-tetra-chloro-3a, 6a-diphenylglycoluril. Biochem Biophys Res Commun 80:849–857

    Google Scholar 

  • George R, Barber DL, Schneider WJ (1987) Characterization of the chicken oocyte receptor for low and very low density lipoproteins. J Biol Chem 262:16838–16847

    Google Scholar 

  • Goldstein JL, Brown MS, Anderson RGW, Russell DW, Schneider WJ (1985) Receptor-mediated endocytosis: Concepts emerging from the LDL receptor system. Annu Rev Cell Biol 1:1–39

    Google Scholar 

  • Griffin HD, Perry MM, Gilbert AB (1984) Yolk formation. In: Freeman BM (ed) Physiology and biochemistry of the domestic fowl. Academic Press, London, pp 345–380

    Google Scholar 

  • Hayashi K, Nimpf J, Schneider WJ (1989a) Chicken oocytes and fibroblasts express different apolipoprotein-B-specific receptors. J Biol Chem 264:3131–3139

    Google Scholar 

  • Hayashi K, Ando S, Stifani S, Schneider WJ (1989b) A novel sterol-regulated surface protein on chicken fibroblasts. J Lipid Res 30:1421–1428

    Google Scholar 

  • Hermier D, Forgez P, Chapman MJ (1985) A density gradient study of the lipoprotein and apolipoprotein distribution in the chicken, Gallus domesticus. Biochem Biophys Acta 836:105–118

    Google Scholar 

  • Herz J, Hamann U, Rogne S, Myklebost O, Gausepohl H, Stanley KK (1988) Surface location and high affinity for calcium of a 500 kD membrane protein closely related to the LDL-receptor suggest a physiological role as lipoprotein receptor. EMBO J 7:4119–4127

    Google Scholar 

  • Jones DG, Briles WE, Schjeide OA (1975) A mutation restricting ovulation in chickens. Poultry Sci 54:1780–1783

    Google Scholar 

  • Mahley RW (1988) Apolipoprotein E: cholesterol transport protein with expanding role in cell biology. Science 240:622–630

    Google Scholar 

  • McGibbon WH (1977) Evidence that the restricted ovulator gene (ro) in the chicken is sex-linked (abstr). Genetics 86:43

    Google Scholar 

  • Nandi PK, Irace G, Jaarsveld PP van, Lippoldt RE, Edelhoch H (1982) Instability of coated vesicles in concentrated sucrose solution. Proc Natl Acad Sci USA 79:5881–5885

    Google Scholar 

  • Nimpf J, George R, Schneider WJ (1988) Apolipoprotein specificity of the chicken oocyte receptor for low and very low density lipoproteins: lack of recognition of apolipoprotein VLDL-II. J Lipid Res 29:657–667

    Google Scholar 

  • Nimpf J, Radosavljevic MJ, Schneider WJ (1989a) Oocytes from the mutant Restricted Ovulator hen lack receptor for very low density lipoprotein. J Biol Chem 264:1393–1398

    Google Scholar 

  • Nimpf J, Radosavljevic M, Schneider WJ (1989b) Specific postendocytic proteolysis of apolipoprotein-B in oocytes does not abolish receptor recognition. Proc Natl Acad Sci USA 86:906–919

    Google Scholar 

  • Opresko LK, Karpf RA (1987) Specific proteolysis regulates fusion between endocytic compartments in Xenopus oocytes. Cell 51:557–568

    Google Scholar 

  • Opresko LK, Wiley HS (1987a) Receptor-mediated endocytosis in Xenopus oocytes. I. Characterization of the vitellogenin receptor system. J Biol Chem 262:4109–4115

    Google Scholar 

  • Opresko LK, Wiley HS (1987b) Receptor-mediated endocytosis in Xenopus oocytes. II. Evidence for two novel mechanisms of hormonal regulation. J Biol Chem 262:4116–4123

    Google Scholar 

  • Pearse BMF (1978) On the structural and functional components of coated vesicles. J Mol Biol 126:803–812

    Google Scholar 

  • Pearse BMF (1982) Coated vesicles from human placenta carry ferritin, transferrin, and immunoglobulin G. Proc natl Acad Sci USA 79:451–455

    Google Scholar 

  • Pearse BMF, Robinson MS (1990) Clathrin, adaptors and sorting. Annu Rev Cell Biol 6:151–171

    Google Scholar 

  • Perry MM, Gilbert AB (1979) Yolk transport in the ovarian follicle of the hen (Gallus domesticus): lipoprotein-like particles at the periphery of the oocyte in the rapid growth phase. J Cell Sci 39:257–272

    Google Scholar 

  • Perry MM, Gilbert AB (1985) The structure of yellow yolk in the domestic fowl. J Ultrastruct Res 90:313–322

    Google Scholar 

  • Retzek H, Steyrer E, Sanders EJ, Nimpf J, Schneider WJ (1992) Cathepsin D: a key enzyme for yolk formation in the chicken oocyte. DNA Cell Biol 11:661–672

    Google Scholar 

  • Roach PD, Zollinger M, Noel S-P (1987) Detection of low density lipoprotein (LDL) receptor on nitrocellulose paper with colloidal gold-LDL conjugates. J Lipid Res 28:1515–1521

    Google Scholar 

  • Schneider WJ, Carroll R, Severson DL, Nimpf J (1990) Apolipoprotein VLDL-II inhibits lipolysis of triglyceride-rich lipoproteins in the laying hen. J Lipid Res 31:507–513

    Google Scholar 

  • Steyrer E, Barber DL, Schneider WJ (1990) Evolution of lipoprotein receptors. J Biol Chem 265:19575–19581

    Google Scholar 

  • Stifani S, George R, Schneider WJ (1988) Solubilization and characterization of the chicken oocyte vitellogenin receptor. Biochem J 250:467–475

    Google Scholar 

  • Stifani S, Barber DL, Nimpf J, Schneider WJ (1990) A single chicken oocyte plasma membrane protein mediates uptake of very low density lipoprotein and vitellogenin. Proc Natl Acad Sci USA 87:1955–1959

    Google Scholar 

  • Stifani S, Barber DL, Aebersold R, Steyrer E, Shen X, Nimpf J, Schneider WJ (1991) The laying hen expresses two different low density lipoprotein receptor-related proteins. J Biol Chem 266:19079–19087

    Google Scholar 

  • Timpl R, Paulsson M, Dziadek M, Fujiwara S (1987) Basement membranes. Methods Enzymol 145:363–391

    Google Scholar 

  • Wall DA, Meleka I (1985) An unusual lysosome compartment involved in vitellogenin endocytosis by Xenopus oocytes. J Cell Biol 101:1651–1664

    Google Scholar 

  • Wall DA, Patel S (1987) The intracellular fate of vitellogenin in Xenopus oocytes is determined by its extracellular concentration during endocytosis. J Biol Chem 262:14779–14789

    Google Scholar 

  • White HB, Merrill AH (1988) Riboflavin-binding proteins. Annu Rev Nutr 8:279–299

    Google Scholar 

  • Woods JW, Woodward MP, Roth TF (1978) Common features of coated vesicles from dissimilar tissues: composition and structure. J Cell Sci 30:87–97

    Google Scholar 

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Shen, X., Steyrer, E., Retzek, H. et al. Chicken oocyte growth: receptor-mediated yolk deposition. Cell Tissue Res 272, 459–471 (1993). https://doi.org/10.1007/BF00318552

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