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Vascular differentiation in the root cortex of peas: Premitotic stages of cytoplasmic reactivation

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Summary

Premitotic stages of experimentally induced vascular differentiation were investigated by confocal laser scanning-fluorescence and electron microscopy. Activation of former quiescent and highly vacuolated cortex cells, observed in living and in fixed tissue, involves a centripetal movement of the nucleus along newly-formed, thick cytoplasmic strands. These traverse the large vacuoles with angles different from the former polar axis, thereby anticipating the orientation of later developing phragmosomes, future divisions, and the course of wound-vascular elements.

A premitotic increase in cellular activity is reflected by the number of mitochondria, rough ER-cisternae, active dictyosomes and dense cytoplasm as well as by shape of nuclei and development of “nucleolar vacuoles”. Microtubules occur in parallel arrays running through the transvacuolar strands and radiating from the nucleus towards the cell wall. They might be responsible for the centripetal movement of the nucleus through the vacuole and/or might participate on the orientation of the plane of a future division. Preprophase bands were not detected in cortex cells of the investigated root region, which prior to wounding were already fully elongated.

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Abbreviations

DiOC:

3,3′-dihexyloxacarbocyanine iodide

LSM:

confocal laserscanning microscope

MSB:

microtubule-stabilizing buffer

References

  • Aloni R, Wolf A (1984) Suppressed buds embedded in the bark across the bole and the occurrence of their circular vessels inFicus religiosa. Am J Bot 71: 1060–1066

    Google Scholar 

  • Bakhuizen R, Spronsen PC van, Sluiman-den Hertog FAJ, Venverloo CJ, Goosen-de Roo L (1985) Nuclear envelope radiating microtubules in plant cells during interphase mitosis transition. Protoplasma 128: 43–51

    Google Scholar 

  • Behnke H-D, Schulz A (1980) Fine structure, pattern of division, and course of wound phloem inColeus blumei. Planta 150: 357–365

    Google Scholar 

  • Gersani M (1985) Appearance of new transport capacity in wounded plants. J Exp Bot 36: 1809–1816

    Google Scholar 

  • Goosen-de Roo L, Bakhuizen R, Spronsen PC van, Libbenga KR (1984) The presence of extended phragmosomes containing cytoskeletal elements in fusiform cambial cells ofFraxinus excelsior L. Protoplasma 122: 145–152

    Google Scholar 

  • Gunning BES (1982) The cytokinetic apparatus: its development and spatial regulation. In:Lloyd (ed) The cytoskeleton. Academic Press, London, pp 229–292

    Google Scholar 

  • Hardham AR, McCully M (1982 a) Reprogramming of cells following wounding in pea (Pisum sativum L.) roots. I. Cell division and differentiation of new vascular elements. Protoplasma 112: 143–151

    Google Scholar 

  • — (1982 b) Reprogramming of cells following wounding in pea (Pisum sativum L.) roots. II. The effects of caffeine and colchicine on the development of new vascular elements. Protoplasma 112: 152–166

    Google Scholar 

  • Heslop-Harrison J, Heslop-Harrison Y (1970) Evaluation of pollen viability by enzymatically induced fluorescence; intracellular hydrolysis of fluorescein diacetate. Stain Techn 45: 115–120

    Google Scholar 

  • Karnovski MJ (1965) A formaldehyde-glutaraldehyde fixative of high osmolality for use in electron microscopy. J Cell Biol 27: 137A-138A

    Google Scholar 

  • Kirschner H, Sachs T (1978) Cytoplasmic reorientation: An early stage of vascular differentiation. Isr J Bot 27: 131–137

    Google Scholar 

  • Matzke MA, Matzke AJM (1986) Visualization of mitochondria and nuclei in living plant cells by the use of a potential-sensitive fluorescent dye. Plant Cell Envir 9: 73–77

    Google Scholar 

  • Pickett-Heaps JD, Northcote DH (1966) Cell division in the formation of the stomatal complex of the young leaves of wheat. J Cell Sci 1: 121–128

    Google Scholar 

  • Quader H, Schnepf E (1986) Endoplasmic reticulum and cytoplasmic streaming: Fluorescence microscopical observations in adaxial epidermis cells of onion bulb scales. Protoplasma 131: 250–252

    Google Scholar 

  • Quader H, Hofmann A, Schnepf E (1987) Shape and movement of the endoplasmic reticulum in onion bulb epidermis cells: possible involvement of actin. Eur J Cell Biol 44: 17–26

    Google Scholar 

  • Rana MA, Gahan PB (1983) A quantitative cytochemical study of determination for xylem-element formation in response to wounding in roots ofPisum sativum L. Planta 157: 307–316

    Google Scholar 

  • Robbertse PJ, McCully M (1979) Regeneration of vascular tissue in wounded pea roots. Planta 145: 167–173

    Google Scholar 

  • Sachs T (1975) The induction of transport channels by auxin. Planta 127: 201–206

    Google Scholar 

  • — (1981) Polarity changes and tissue organization in plants. In:Schweiger HG (ed) International cell biology 1980/81. Springer, Heidelberg, pp 489–496

    Google Scholar 

  • — (1984) Axiality and polarity in vascular plants. In:Barlow PW, Carr DJ (eds) Positional controls in plant development. Cambridge University Press, Cambridge New York New Rochelle Melbourne Sydney, pp 193–224

    Google Scholar 

  • —,Cohen D (1982) Circular vessels and the control of vascular differentiation in plants. Differentiation 21: 22–26

    Google Scholar 

  • Schmiedel G, Schnepf E (1979) Side branch formation and orientation in the caulonema of the moss,Funaria hygrometrica: Normal development and fine structure. Protoplasma 100, 367–383

    Google Scholar 

  • Schnepf E, Traitteur R von (1973) Über die traumatotaktische Bewegung der Zellkerne inTradescantia-Blättern. Z Pflanzenphysiol 69: 181–184

    Google Scholar 

  • Schulz A (1986) Wound phloem in transition to bundle phloem in primary roots ofPisum sativum L.: I. Development of bundle-leaving wound-sieve tubes. Protoplasma 130: 12–26

    Google Scholar 

  • — (1987) Sieve element differentiation and fluoresceine translocation in wound-phloem of pea roots after complete severance of the stele. Planta 170: 289–299

    Google Scholar 

  • Sinnott EW, Bloch R (1941) Division in vacuolate plant cells. Am J Bot 28: 225–232

    Google Scholar 

  • Venverloo CJ, Hovenkamp PH, Weeda AJ, Libbenga KR (1980) Cell divisions inNautilocalyx explants I. Phragmosome, preprophase band and plane of division. Z Pflanzenphysiol 100: 161–174

    Google Scholar 

  • White JG, Amos WB, Fordham M (1987) An evaluation of confocal versus conventional imaging of biological structures by fluorescence light microscopy. J Cell Biol 105: 41–48

    Google Scholar 

  • Wick SM, Duniec J (1983): Immunofluorescence microscopy of tubulin and microtubule arrays in plant cells. I. Preprophase band development and concomitant appearance of nuclear envelope-associated tubulin. J Cell Biol 97: 235–243

    Google Scholar 

  • — (1984) Immunofluorescence microscopy of tubulin and microtubule arrays in plant cells. II. Transition between Preprophase band and the mitotic spindle. Protoplasma 122: 45–55

    Google Scholar 

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Schulz, A. Vascular differentiation in the root cortex of peas: Premitotic stages of cytoplasmic reactivation. Protoplasma 143, 176–187 (1988). https://doi.org/10.1007/BF01291162

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