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Cell shaping and microtubules in developing mesophyll of wheat (Triticum aestivum L.)

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Summary

Differentiated mesophyll cells ofTriticum aestivum (cv. Star) exhibit a lobed outline resembling tube-shaped balloons with almost regularly spaced constrictions. It was shown that these constrictions are probably the result of hoops of wall reinforcements laid down during early stages of cell expansion. It appears that these hoops prevent expansion in the corresponding regions and thus give rise to the peculiar cell shape. The comparatively thin cell walls of the bulges are uniformly reinforced after the lobed shape is established.

By using immunofluorescence techniques a change in the pattern of cortical microtubule arrangement was observed which corresponded to the pattern of cell wall deposition. Discrete bands of microtubules were found beneath the sites of hoop reinforcement. These bands disintegrated during late stages of cell expansion with microtubules fanning out into the almost empty regions of the bulges.

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Abbreviations

DMSO:

dimethyl sulfoxid

EGTA:

ethylene glycol bis-(β-aminoethyl ether) N,N,N′,N′-tetraacetic acid

FITC:

fluorescein isothiocyanat

MSB:

microtubule stabilizing buffer

PBS:

phosphate buffered saline

PIPES:

1,4-piperazine diethanesulfonic acid

PMSF:

phenylmethyl sulfonylfluoride

References

  • Falconer MM, Seagull RW (1985) Xylogenesis in tissue culture: taxol effects on microtubule reorientation and lateral association in differentiating cells. Protoplasma 128: 157–166

    Google Scholar 

  • Gerstenberger P, Leins P (1978) Rasterelektronenmikroskopische Untersuchungen an Blütenknospen vonPhysalis philadelphica (Solanaceae). Anwendung einer neuen Präparationsmethode. Ber Deutsch Bot Ges 91: 381–387

    Google Scholar 

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

    Google Scholar 

  • Hardham AR, Gunning BES (1979) Interpolation of microtubules into cortical arrays during cell elongation and differentiation in roots ofAzolla pinnata. J Cell Sci 37: 411–442

    Google Scholar 

  • Hepler PK, Fosket DE (1971) The role of microtubules in vessel member differentiation inColeus. Protoplasma 72: 213–236

    Google Scholar 

  • —, Palevitz BA (1974) Microtubules and microfilaments. Ann Rev Plant Physiol 25: 309–362

    Google Scholar 

  • Iwata K, Hogetsu T (1988) Arrangement of cortical microtubules inAvena coleoptiles and mesocotyls andPisum epicotyls. Plant Cell Physiol 29: 807–815

    Google Scholar 

  • Kobayashi H, Fukuda H, Shibaoka H (1988) Interrelation between the spatial disposition of actin filaments and microtubules during the differentiation of tracheary elements in culturedZinnia cells. Protoplasma 143: 29–37

    Google Scholar 

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

    Google Scholar 

  • —, Wells B (1985) Microtubules are at the tips of root hairs and form helical patterns corresponding to inner wall fibrils. J Cell Sci 75: 225–238

    Google Scholar 

  • Mayer RJ, Walker JH (1987) Immunochemical methods in cell and molecular biology. Academic Press, London San Diego

    Google Scholar 

  • Palevitz BA, Hepler PK (1976) Cellulose microfibril orientation and cell shaping in developing guard cells ofAllium: the role of microtubules and ion accumulation. Planta 132: 71–93

    Google Scholar 

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

    Google Scholar 

  • Quader H, Deichgräber G, Schnepf E (1986) The cytoskeleton ofCobaea seed hairs: patterning during cell-wall differentiation. Planta 168: 1–10

    Google Scholar 

  • Seagull RW (1989) The plant cytoskeleton. CRC Crit Rev Plant Sci 8: 131–167

    Google Scholar 

  • Schneider B, Herth W (1986) Distribution of plasma membrane rosettes and kinetics of cellulose formation in xylem development of higher plants. Protoplasma 131: 142–152

    Google Scholar 

  • Schnepf E (1973) Microtubulus-Anordnung und -Umordnung, Wandbildung und Zellmorphogenese in jungenSphagnum-Blättchen. Protoplasma 78: 145–173

    Google Scholar 

  • Sinnott EW, Bloch R (1945) The cytoplasmic basis of intercellular patterns in vascular differentiation. Am J Bot 32: 151–156

    Google Scholar 

  • Valk HC van der, Blaas J, Eck JW van, Verhoeven HA (1988) Vital DNA staining of agarose-embedded protoplasts and cell suspensions ofNicotiana plumbaginifolia. Plant Cell Rep 7: 489–492

    Google Scholar 

  • Wernicke W, Milkovits L (1984) Developmental gradients in wheat leaves-response of leaf segements in different genotypes cultured in vitro. J Plant Physiol 115: 49–58

    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 

  • —, 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

    Google Scholar 

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Jung, G., Wernicke, W. Cell shaping and microtubules in developing mesophyll of wheat (Triticum aestivum L.). Protoplasma 153, 141–148 (1990). https://doi.org/10.1007/BF01353998

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  • DOI: https://doi.org/10.1007/BF01353998

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