Lentil root statoliths reach a stable state in microgravity

• Published in: Planta 2000-08, Vol.211 (3), p.396-405
• Main Authors: Driss-Ecole, Dominique, Jeune, Bernard, Prouteau, Monique, Julianus, Philippe, Perbal, Gérald
• Format: Article
• Language: English
• Subjects: Actins; Agronomy. Soil science and plant productions; Amyloplasts; Biological and medical sciences; Cell walls; Centrifugation; Cytochalasins; Economic plant physiology; Fabaceae - cytology; Fabaceae - growth & development; Fabaceae - physiology; Fundamental and applied biological sciences. Psychology; Lentils; Microfilaments; Microgravity; Movements; Plant physiology and development; Plant roots; Plant Roots - cytology; Plant Roots - physiology; Plant Roots - ultrastructure; Plants, Medicinal; Seedlings; Space Flight; Space life sciences; Time Factors; Tropism and nastic movements; Weightlessness
• ISSN: 0032-0935; 1432-2048
• DOI: 10.1007/s004250000298

The kinetics of the movement of statoliths in gravity-perceiving root cap cells of Lens culinaris L. and the force responsible for it have been analysed under 1 g and under microgravity conditions (S/MM-03 mission of Spacehab 1996). At the beginning of the experiment in space, the amyloplasts were grouped at the distal pole of the statocytes by a root-tip-directed 1-g centrifugal acceleration. The seedlings were then placed in microgravity for increasing periods of time (13, 29, 46 or 122 min) and chemically fixed. During the first 29 min of microgravity there were local displacements (mean velocity: 0.154 μm min-1) of some amyloplasts (first at the front of the group and then at the rear). Nevertheless, the group of amyloplasts tended to reconstitute. After 122 min in microgravity the bulk of amyloplasts had almost reached the proximal pole where further movement was blocked by the nucleus. After a longer period in microgravity (4 h; experiment carried out 1994 during the IML 2 mission) the statoliths reached a stable position due to the fact that they were stopped by the nucleus. The position was similar to that observed in roots grown continuously in microgravity. Treatment with cytochalasin D (CD) did not stop the movement of the amyloplasts but slowed down the velocity of their displacement (0.019 μm min-1). Initial movement patterns were the same as in control roots in water. Comparisons of mean velocities of amyloplast movements in roots in space and in inverted roots on earth showed that the force responsible for the movement in microgravity (Fc) was about 86% less (Fc = 0.016 pN) than the gravity force (Fg = 0.11 pN). Treatment with CD reduced Fc by two-thirds. The apparent viscosity of the statocyte cytoplasm was found to be 1 Pa s or 3.3 Pa s for control roots or CD treated roots, respectively. Brownian motion or elastic forces due to endoplasmic reticulum membranes do not cause the movement of the amyloplasts in microgravity. It concluded that the force transporting the statoliths caused by the actomyosin system.