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Changes in the lysosome structure during the formation of zoospores inTrebouxia potteri

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Summary

Changes in the lysosome structures were examined by electron microscopy during the formation of zoospores inTrebouxia potteri. Lysosomes in vegetative cells were homogeneously filled with electron-dense material. At the beginning of zoospore formation, lysosomes invaginated or evaginated to take up mitochondria, ER, or cytoplasmic ground plasma. The ingested organelles became disorganized within the lysosomes. During this disruption of these organelles, the lysosomal contents became heterogeneous, suggesting a decrease in the amount of enzymes within the lysosomes. Golgi bodies and ER seemed to be involved with the disruption of the organelles, probably supplying some substances necessary for the functioning of the lysosomes. Amount of electron-dense materials decreased and, finally, only one to three small spherical aggregates remained in the lysosomes. Then the lysosomes appeared to shrink via loss of watery substances or cutting off of electron-transparent regions. After these changes in lysosome structure, nuclei started to divide successively for formation of the zoospores. The possibility is proposed that the drastic cytoplasmic changes operated by lysosomes trigger the following morphogenetic events in the formation of zoospores.

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Abbreviations

ER:

endoplasmic reticulum

TGN:

trans Golgi network

References

  • Bainton D (1981) The discovery of lysosomes. J Cell Biol 91: 66s-76s

    PubMed  Google Scholar 

  • Berjak P (1972) Lysosomal compartmentation: ultrastructural aspects of the origin, development and function of vacuoles inLepidium sativum. Ann Bot 36: 73–81

    Google Scholar 

  • Chida Y, Ueda K (1991) Division of chloroplasts in a green alga,Trebouxia potteri. Ann Bot 67: 435–442

    Google Scholar 

  • Fineran BA (1972) Ultrastructure of vacuolar inclusions in root tips. Protoplasma 72: 1–18

    Google Scholar 

  • Gray RH, Brabec RK, Cox SG, Foster PW, Bernstein IA (1974) The ultrastructural localization of glucose-6-phosphatase and possible origin of concentric membranes of hepatic autophagic vacuoles. J Cell Biol 63: 120 a

    Google Scholar 

  • Hara-Nishimura I, Hayashi M, Nishimura M, Akazawa T (1987) Biogenesis of protein bodies by budding from vacuoles in developing pumpkin cotyledons. Protoplasma 136: 49–55

    Google Scholar 

  • Ichimura T (1971) Sexual cell division and conjugation-papilla formation in sexual reproduction ofClosterium strigosum. In: Nishizawa K et al (eds) Proceedings of the 7th International Seaweed Symposium. University of Tokyo Press, Tokyo, pp 208–214

    Google Scholar 

  • Leedale GF, Buetow DE (1976) Observations on cytolysome formation and other cytological phenomena in carbon-starvedEuglena gracilis. J Microsc Biol Cell 25: 149–154

    Google Scholar 

  • Locke M, McMahon JT (1971) The origin and fate of microbodies in the fat body of an insect. J Cell Biol 48: 61–78

    PubMed  Google Scholar 

  • Marty F (1970) Rôle du système membranaire vacuolarie dans la differéntiation des laticifères d'Euphorbia characians L. CR Acad Sci D 271: 2301–2304

    Google Scholar 

  • — (1978) Cytochemical studies on GERL, provacuoles, and vacuoles in root meristematic cells ofEuphorbia. Proc Natl Acad Sci USA 75: 852–856

    Google Scholar 

  • Marzella L, Ahlberg J, Glaumann H (1980) In vitro uptake of particles by lysosomes. Exp Cell Res 129: 460–466

    PubMed  Google Scholar 

  • Matile P (1975) The lytic compartment of plant cells. Springer, Wien New York [Alfert M et al (eds) Cell biology monographs, vol 1]

    Google Scholar 

  • — (1978) Biochemistry and function of vacuoles. Annu Rev Plant Physiol 29: 193–213

    Google Scholar 

  • Mayahara H, Chang JP (1978) Electron microscopic study of acid phosphatase activity in cultured human cystic fibrosis fibroblasts. Acta Histochem Cytochem 11: 449–459

    Google Scholar 

  • Mesquita JF (1972) Ultrastructure de formations comparables aux vacuoles autophagiques dans les cellules des racines de l'Allium cepa L. et duLupinus albus L. Cytologia 37: 95–110

    Google Scholar 

  • Nishimura M, Beevers H (1978) Hydrolases in vacuoles from castor bean endosperm. Plant Physiol 62: 44–48

    Google Scholar 

  • Noguchi T (1976) Phosphatase activities and osmium reduction in cell organelles ofMicrasterias americana. Protoplasma 87: 163–178

    PubMed  Google Scholar 

  • — (1990) Consumption of lipid granules and formation of vacuoles in the pollen tube ofTradescantia reflexa. Protoplasma 156: 19–28

    Google Scholar 

  • Novikoff AB, Shin WY (1978) Endoplasmic reticulum and autophagy in rat hepatocytes. Proc Natl Acad Sci USA 75: 5039–5042

    PubMed  Google Scholar 

  • Peoples MB, Beilharz VC, Waters SP, Simpson RJ, Dalling MJ (1980) Nitrogen redistribution during grain growth in wheat (Triticum sativum L.). II. Chloroplast senescence and the degradation of ribulose-1,5-bisphosphate carboxylase. Planta 149: 241–251

    Google Scholar 

  • Reunanen H, Hirsimäki P (1983) Studies on vinblastine-induced autophagocytosis in mouse liver. IV. Origin of membranes. Histochemistry 79: 59–67

    PubMed  Google Scholar 

  • Saito T, Ogawa K (1974) Lysosomal changes in rat hepatic parenchymal cells after glucagon administration. Acta Histochem Cytochem 7: 1–8

    Google Scholar 

  • Sakai M, Ogawa K (1984) Relationship between lysosomal wrapping mechanism (LWM) and cytoskeletal elements during autophagolysosome formation. Acta Histochem Cytochem 17: 1–14

    Google Scholar 

  • Smith RE, Farquhar MG (1966) Lysosome function in the regulation of the secretory process in cells of the anterior pituitary gland. J Cell Biol 31: 319–347

    Google Scholar 

  • Tan K, Ueda K (1978) Rapid degeneration of the protoplasm in artificially induced small cells ofMicrasterias crux melitensis. Protoplasma 97: 61–70

    Google Scholar 

  • Vaughn KC, Duke SO (1981) Evaginations from the plastid envelope: a method for transfer of substances from plastid to vacuole. Cytobios 32: 89–95

    Google Scholar 

  • Villiers TA (1971 a) Lysosomal activities of the vacuole in damaged and recovering plant cells. Nature New Biol 233: 57–58

    PubMed  Google Scholar 

  • — (1971 b) Cytology studies in dormancy. II. Pathological ageing changes during prolonged dormancy and recovery upon dormancy release. New Phytol 71: 145–152

    Google Scholar 

  • von Figura K, Hasilik A (1986) Lysosomal enzymes and their receptors. Annu Rev Biochem 55: 167–193

    PubMed  Google Scholar 

  • Vorbrodt A, Gruca S, Gruca-Krzyzowska S (1971) Cytochemical studies on the participation of endoplasmic reticulum in the formation of lysosomes (dense bodies) in rat hepatocytes. J Microscopie 12: 73–82

    Google Scholar 

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Chida, Y., Ueda, K. Changes in the lysosome structure during the formation of zoospores inTrebouxia potteri . Protoplasma 171, 19–27 (1992). https://doi.org/10.1007/BF01379276

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  • DOI: https://doi.org/10.1007/BF01379276

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