Close Temporal Relationship between Oscillating Cytosolic K+ and Growth in Root Hairs of Arabidopsis

Root hair elongation relies on polarized cell expansion at the growing tip. As a major osmotically active ion, potassium is expected to be continuously assimilated to maintain cell turgor during hair tip growth. However, due to the lack of practicable detection methods, the dynamics and physiological role of K+ in hair growth are still unclear. In this report, we apply the small-molecule fluorescent K+ sensor NK3 in Arabidopsis root hairs for the first time. By employing NK3, oscillating cytoplasmic K+ dynamics can be resolved at the tip of growing root hairs, similar to the growth oscillation pattern. Cross-correlation analysis indicates that K+ oscillation leads the growth oscillations by approximately 1.5 s. Artificially increasing cytoplasmic K+ level showed no significant influence on hair growth rate, but led to the formation of swelling structures at the tip, an increase of cytosolic Ca2+ level and microfilament depolymerization, implying the involvement of antagonistic regulatory factors (e.g., Ca2+ signaling) in the causality between cytoplasmic K+ and hair growth. These results suggest that, in each round of oscillating root hair elongation, the oscillatory cell expansion accelerates on the heels of cytosolic K+ increment, and decelerates with the activation of antagonistic regulators, thus forming a negative feedback loop which ensures the normal growth of root hairs.

Osmophoresis - a possible mechanism for vesicle trafficking in tip-growing cells

A mechanism for polarized transport of vesicles by means of osmotic propulsions is proposed and substantiated for tip-growing cells. An analysis is presented which shows that in pollen tubes the gradient of cytosolic water potential can drive vesicle movement either in the anterograde or retrograde direction, depending on the vesicle position, its radius and the phase of growth oscillation. The importance of transcellular water flow for cytoskeletal dynamics and cell motility is highlighted.

Growth oscillation in larger foraminifera

This work shows the potential for applying three-dimensional biometry to studying cell growth in larger benthic foraminifera. The volume of each test chamber was measured from the three-dimensional model obtained by means of computed tomography. Analyses of cell growth based on the sequence of chamber volumes revealed constant and significant oscillations for all investigated specimens, characterized by periods of approximately 15, 30, 90, and 360 days. Possible explanations for these periods are connected to tides, lunar cycles, and seasonality. The potential to record environmental oscillations or fluctuations during the lifetime of larger foraminifera is pivotal for reconstructing short-term paleoenvironmental variations or for gaining insight into the influence of tides or tidal current on the shallow-water benthic fauna in both recent and fossil environments.

Growth, oscillation and collapse of vortex cavitation bubbles

The growth, oscillation and collapse of vortex cavitation bubbles are examined using both two- and three-dimensional numerical models. As the bubble changes volume within the core of the vortex, the vorticity distribution of the surrounding flow is modified, which then changes the pressures at the bubble interface. This interaction can be complex. In the case of cylindrical cavitation bubbles, the bubble radius will oscillate as the bubble grows or collapses. The period of this oscillation is of the order of the vortex time scale, τV = 2πrc/uθ, max, where rc is the vortex core radius and uθ, max is its maximum tangential velocity. However, the period, oscillation amplitude and final bubble radius are sensitive to variations in the vortex properties and the rate and magnitude of the pressure reduction or increase. The growth and collapse of three-dimensional bubbles are reminiscent of the two-dimensional bubble dynamics. But, the axial and radial growth of the vortex bubbles are often strongly coupled, especially near the axial extents of the bubble. As an initially spherical nucleus grows into an elongated bubble, it may take on complex shapes and have volume oscillations that also scale with τV. Axial flow produced at the ends of the bubble can produce local pinching and fission of the elongated bubble. Again, small changes in flow parameters can result in substantial changes to the detailed volume history of the bubbles.

Oscillatory ROP GTPase Activation Leads the Oscillatory Polarized Growth of Pollen Tubes

Oscillation regulates a wide variety of processes ranging from chemotaxis in Dictyostelium through segmentation in vertebrate development to circadian rhythms. Most studies on the molecular mechanisms underlying oscillation have focused on processes requiring a rhythmic change in gene expression, which usually exhibit a periodicity of >10 min. Mechanisms that control oscillation with shorter periods (<10 min), presumably independent of gene expression changes, are poorly understood. Oscillatory pollen tube tip growth provides an excellent model to investigate such mechanisms. It is well established that ROP1, a Rho-like GTPase from plants, plays an essential role in polarized tip growth in pollen tubes. In this article, we demonstrate that tip-localized ROP1 GTPase activity oscillates in the same frequency with growth oscillation, and leads growth both spatially and temporally. Tip growth requires the coordinate action of two ROP1 downstream pathways that promote the accumulation of tip-localized Ca2+and actin microfilaments (F-actin), respectively. We show that the ROP1 activity oscillates in a similar phase with the apical F-actin but apparently ahead of tip-localized Ca2+. Furthermore, our observations support the hypothesis that the oscillation of tip-localized ROP activity and ROP-dependent tip growth in pollen tubes is modulated by the two temporally coordinated downstream pathways, an early F-actin assembly pathway and a delayed Ca2+gradient-forming pathway. To our knowledge, our report is the first to demonstrate the oscillation of Rho GTPase signaling, which may be a common mechanism underlying the oscillation of actin-dependent processes such as polar growth, cell movement, and chemotaxis.