Skip to main content
Log in

Root contraction in hyacinth IV. Orientation of cellulose microfibrils in radial longitudinal and transverse cell walls

  • Published:
Protoplasma Aims and scope Submit manuscript

Summary

Cellulose microfibrils (MFs) were visualized on the inner surface of root cortex cell walls ofHyacinthus orientalis L. using a replica technique. Microfibril orientation was determined in radial longitudinal and transverse cell walls of the root tip, uncontracted, contracting, and fully contracted regions of the root. In longitudinal walls, the innermost MFs were ordered and parallel to one another and were oriented transversely, axially or obliquely, depending upon the developmental stage of the region. In transverse walls MFs in a single layer formed crisscross or ordered parallel arrays, depending upon the region. Parallel arrays were oriented either parallel, perpendicular, or oblique to the radius of the root. Inner walls of certain cells in the contracting region had MFs which appeared interrupted over their lengths. In general, these findings parallel earlier immunofluorescence and electron microscopic observations of changing cortical microtubule (MT) orientation accompanying root contraction. The major exception to MT-MF congruence occurred in cells of the actively contracting region. In middle and outer cell layers, MFs appeared short and partially obscured, while MTs in these cells occurred in conspicuous laterally aggregated strands parallel to one another over the length of the cells or were absent. This alteration in MF-MT parallelism may be related to the reorientation in cell growth occurring in the contractile zone or to the collapse of specific cells during the process of root contraction.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

MF:

microfibril

MT:

microtubule

References

  • Cyr RJ, Lin B-L, Jernstedt JA (1988) Root contraction in hyacinth. II. Changes in tubulin levels, microtubule number and orientation associated with differential cell expansion. Planta 174: 446–452

    Google Scholar 

  • Gunning BES, Hardham AR (1982) Microtubules. Annu Rev Plant Physiol 33: 651–698

    Google Scholar 

  • Hardham AR (1982) Regulation of polarity in tissues and organs. In: Lloyd CW (ed) The cytoskeleton in plant growth and development. Academic Press, London, pp 377–403

    Google Scholar 

  • Hogetsu T (1986) Orientation of wall microfibril deposition in root cells ofPisum sativum L. var Alaska. Plant Cell Physiol 27: 947–951

    Google Scholar 

  • —, Oshima Y (1986) Immunofluorescence microscopy of microtubule arrangement in root cells ofPisum sativum L. var Alaska. Plant Cell Physiol 27: 939–945

    Google Scholar 

  • Jernstedt JA (1984) Root contraction in hyacinth. I. Effects of IAA on differential cell expansion. Amer J Bot 71: 1080–1089

    Google Scholar 

  • Lang JM, Eisinger WR, Green PB (1982) Effects of ethylene on the orientation of microtubules and cellulose microfibrils of pea epicotyl cells with polylamellate cell walls. Protoplasma 110: 5–14

    Google Scholar 

  • Lin B-L, Jernstedt JA (1987) Microtubule organization in root cortical cells ofHyacinthus orientalis. Protoplasma 141: 13–23

    Google Scholar 

  • Lloyd CW (1984) Toward a dynamic helical model for the influence of microtubules on wall patterns in plants. Int Rev Cytol 86: 1–51

    Google Scholar 

  • — (1987) The plant cytoskeleton: the impact of fluorescence microscopy. Annu Rev Plant Physiol 38: 119–139

    Google Scholar 

  • —, Barlow PW (1982) The coordination of cell division and elongation: the role of the cytoskeleton. In: Lloyd CW (ed) The cytoskeleton in plant growth and development. Academic Press, London, pp 103–228

    Google Scholar 

  • Marchant HJ (1982) The establishment and maintenance of plant cell shape by microtubules. In: Lloyd CW (ed) The cytoskeleton in plant growth and development. Academic Press, London, pp 295–319

    Google Scholar 

  • Mita I, Shibaoka H (1984 a) Effects of root excision on swelling of leaf sheath cells and on the arrangement of cortical microtubules in onion seedlings. Plant Cell Physiol 25: 1521–1529

    Google Scholar 

  • — — (1984 b) Effects of S-3307, an inhibitor of gibberellin biosynthesis, on swelling of leaf sheath cells and on the arrangement of cortical microtubules in onion seedlings. Plant Cell Physiol 25: 1531–1539

    Google Scholar 

  • — — (1984 c) Gibberellin stabilizes microtubules in onion leaf sheath cells. Protoplasma 119: 100–109

    Google Scholar 

  • Mueller SC, Brown RM Jr (1982) The control of cellulose microfibril deposition in the cell wall of higher plants. I. Can directed membrane flow orient cellulose microfibrils? Indirect evidence from freeze-fractured plasma membranes of maize and pine seedlings. Planta 154: 489–500

    Google Scholar 

  • Preston RD (1988) Cellulose-microfibril-orienting mechanisms in plant cell walls. Planta 174: 67–74

    Google Scholar 

  • Quader H (1986) Cellulose microfibril orientation inOocystis solitaria: proof that microtubules control the alignment of the terminal complexes. J Cell Sci 83: 223–234

    PubMed  Google Scholar 

  • Richmond PA (1983) Patterns of cellulose microfibril deposition and rearrangement inNitella: in vivo analysis by a birefringence index. J Appl Polym Sci: Appl Polym Symp 37: 107–122

    Google Scholar 

  • —, Métraux J-P (1984) Cellulose synthesis inhibition, cell expansion, and patterns of cell wall deposition inNitella internodes. In: Dugger WM, Bartnicki-Garcia S (eds) Structure, function, and biosynthesis of plant cell walls. Proceedings of the Seventh Annual Symposium in Botany, University of California, Riverside, pp 475–476

    Google Scholar 

  • Roberts IN, Lloyd CW, Roberts K (1985) Ethylene-induced microtubule reorientations: mediation by helical arrays. Planta 164: 439–447

    Google Scholar 

  • Smith-Huerta NL, Jernstedt JA (1989) Root contraction in hyacinth III. Orientation of cortical microtubules visualized by immunofluorescence microscopy. Protoplasma 151: 1–10

    Google Scholar 

  • Sterling C (1972) Mechanism of root contraction inGladiolus. Ann Bot 36 (ns): 599–603

    Google Scholar 

  • Taiz L (1984) Plant cell expansion: regulation of cell wall mechanical properties. Annu Rev Plant Physiol 35: 585–657

    Google Scholar 

  • Traas JA, Braat P, Derksen JW (1984) Changes in microtubule arrays during the differentiation of cortical root cells ofRaphanus sativus. Eur J Cell Biol 34: 229–238

    PubMed  Google Scholar 

  • Wick SM (1985) Immunofluorescence microscopy of tubulin and microtubule arrays in plant cells. III. Transition between mitotic/cytokinetic and interphase microtubule arrays. Cell Biol Int Rep 9: 357–371

    PubMed  Google Scholar 

  • —, Seagull RW, Osborn M, Weber K, Gunning BES (1981) Immunofluorescence microscopy of organized microtubule arrays in structurally stabilized meristematic plant cells. J Cell Biol 89: 685–690

    PubMed  Google Scholar 

  • Wilson K, Honey JN (1966) Root contraction inHyacinthus orientalis. Ann Bot 30: 47–61

    Google Scholar 

  • Zamski E, Ucko O, Koller D (1983) The mechanism of root contraction inGymnarrhena micranatha, a desert plant. New Phytol 95: 29–35

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Smith-Huerta, N.L., Jernstedt, J.A. Root contraction in hyacinth IV. Orientation of cellulose microfibrils in radial longitudinal and transverse cell walls. Protoplasma 154, 161–171 (1990). https://doi.org/10.1007/BF01539844

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01539844

Keywords

Navigation