Literature DB >> 11541080

Centrifugation causes adaptation of microfilaments: studies on the transport of statoliths in gravity sensing Chara rhizoids.

M Braun1, A Sievers.   

Abstract

The actin cytoskeleton is involved in the positioning of statoliths in tip growing Chara rhizoids. The balance between the acropetally acting gravity force and the basipetally acting net outcome of cytoskeletal force results in the dynamically stable position of the statoliths 10-30 micrometers above the cell tip. A change of the direction and/or the amount of one of these forces in a vertically growing rhizoid results in a dislocation of statoliths. Centrifugation was used as a tool to study the characteristics of the interaction between statoliths and microfilaments (MFs). Acropetal and basipetal accelerations up to 6.5 g were applied with the newly constructed slow-rotating-centrifuge-microscope (NIZEMI). Higher accelerations were applied by means of a conventional centrifuge, namely acropetally 10-200 g and basipetally 10-70 g. During acropetal accelerations (1.4-6g), statoliths were displaced to a new stable position nearer to the cell vertex (12-6.5 micrometers distance to the apical cell wall, respectively), but they did not sediment on the apical cell wall. The original position of the statoliths was reestablished within 30 s after centrifugation. Sedimentation of statoliths and reduction of the growth rates of the rhizoids were observed during acropetal accelerations higher than 50 g. When not only the amount but also the direction of the acceleration were changed in comparison to the natural condition, i.e., during basipetal accelerations (1.0-6.5 g), statoliths were displaced into the subapical zone (up to 90 micrometers distance to the apical cell wall); after 15-20 min the retransport of statoliths to the apex against the direction of acceleration started. Finally, the natural position in the tip was reestablished against the direction of continuous centrifugation. Retransport was observed during accelerations up to 70 g. Under the 1 g condition that followed the retransported statoliths showed an up to 5-fold increase in sedimentation time onto the lateral cell wall when placed horizontally. During basipetal centrifugations > or = 70 g all statoliths entered the basal vacuolar part of the rhizoid where they were cotransported in the streaming cytoplasm. It is concluded that the MF system is able to adapt to higher mass accelerations and that the MF system of the polarly growing rhizoid is polarly organized.

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Year:  1993        PMID: 11541080     DOI: 10.1007/bf01404042

Source DB:  PubMed          Journal:  Protoplasma        ISSN: 0033-183X            Impact factor:   3.356


  22 in total

1.  Oriented movement of statoliths studied in a reduced gravitational field during parabolic flights of rockets.

Authors:  D Volkmann; B Buchen; Z Hejnowicz; M Tewinkel; A Sievers
Journal:  Planta       Date:  1991       Impact factor: 4.116

2.  Statoliths and microfilaments in plant cells.

Authors:  A Sievers; S Kruse; L L Kuo-Huang; M Wendt
Journal:  Planta       Date:  1989-09       Impact factor: 4.116

3.  Regulation of the position of statoliths in Chara rhizoids.

Authors:  Z Hejnowicz; A Sievers
Journal:  Protoplasma       Date:  1981       Impact factor: 3.356

4.  Myosin and Ca2+-sensitive streaming in the alga Chara: detection of two polypeptides reacting with a monoclonal anti-myosin and their localization in the streaming endoplasm.

Authors:  F Grolig; R E Williamson; J Parke; C Miller; B H Anderton
Journal:  Eur J Cell Biol       Date:  1988-10       Impact factor: 4.492

5.  [An attempt at a causal analysis of the geotropical reaction chain in the Chara rhizoid].

Authors:  A Sievers; K Schröter
Journal:  Planta       Date:  1971-12       Impact factor: 4.116

6.  The rates of formation and dissociation of actin-myosin complexes. Effects of solvent, temperature, nucleotide binding and head-head interactions.

Authors:  S B Marston
Journal:  Biochem J       Date:  1982-05-01       Impact factor: 3.857

7.  Statoliths pull on microfilaments: experiments under microgravity.

Authors:  B Buchen; M Braun; Z Hejnowicz; A Sievers
Journal:  Protoplasma       Date:  1993       Impact factor: 3.356

8.  Propulsion of organelles isolated from Acanthamoeba along actin filaments by myosin-I.

Authors:  R J Adams; T D Pollard
Journal:  Nature       Date:  1986 Aug 21-27       Impact factor: 49.962

9.  Mechanism of retraction of the trailing edge during fibroblast movement.

Authors:  W T Chen
Journal:  J Cell Biol       Date:  1981-07       Impact factor: 10.539

10.  Direct proof that the primary site of action of cytochalasin on cell motility processes is actin.

Authors:  H Ohmori; S Toyama; S Toyama
Journal:  J Cell Biol       Date:  1992-02       Impact factor: 10.539

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  16 in total

1.  Association of spectrin-like proteins with the actin-organized aggregate of endoplasmic reticulum in the Spitzenkörper of gravitropically tip-growing plant cells.

Authors:  M Braun
Journal:  Plant Physiol       Date:  2001-04       Impact factor: 8.340

2.  The response to gravity is correlated with the number of statoliths in Chara rhizoids.

Authors:  J Z Kiss
Journal:  Plant Physiol       Date:  1994       Impact factor: 8.340

3.  Variation in velocity of cytoplasmic streaming and gravity effect in characean internodal cells measured by laser-Doppler-velocimetry.

Authors:  D Ackers; Z Hejnowicz; A Sievers
Journal:  Protoplasma       Date:  1994       Impact factor: 3.356

4.  Negative gravitropism in Chara protonemata: a model integrating the opposite gravitropic responses of protonemata and rhizoids.

Authors:  D Hodick
Journal:  Planta       Date:  1994-11       Impact factor: 4.116

5.  The density of apical cells of dark-grown protonemata of the moss Ceratodon purpureus.

Authors:  J M Schwuchow; V D Kern; T Wagner; F D Sack
Journal:  Protoplasma       Date:  2000       Impact factor: 3.356

6.  Anomalous gravitropic response of Chara rhizoids during enhanced accelerations.

Authors:  M Braun
Journal:  Planta       Date:  1996-07       Impact factor: 4.116

7.  Hypergravity can reduce but not enhance the gravitropic response of Chara globularis protonemata.

Authors:  D Hodick; A Sievers
Journal:  Protoplasma       Date:  1998       Impact factor: 3.356

Review 8.  Rhizoids and protonemata of characean algae: model cells for research on polarized growth and plant gravity sensing.

Authors:  M Braun; C Limbach
Journal:  Protoplasma       Date:  2006-12-16       Impact factor: 3.356

9.  Halotolerance is enhanced in carrot callus by sensing hypergravity: influence of calcium modulators and cytochalasin D.

Authors:  G F E Scherer
Journal:  Protoplasma       Date:  2006-12-16       Impact factor: 3.356

10.  Suborganellar localisation and effect of light on Helianthus tuberosus chloroplast transglutaminases and their substrates.

Authors:  L Dondini; S Del Duca; L Dall'Agata; R Bassi; M Gastaldelli; M Della Mea; A Di Sandro; I Claparols; D Serafini-Fracassini
Journal:  Planta       Date:  2003-03-14       Impact factor: 4.116

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