Mechanosensory ion channels in Chara: the influence of cell turgor pressure on touch-activated receptor potentials and action potentials

2001 ◽  
Vol 28 (7) ◽  
pp. 551 ◽  
Author(s):  
Virginia A. Shepherd ◽  
Teruo Shimmen ◽  
Mary J. Beilby

Chara cells produce receptor potentials (RPDs) in response to mechanical stimulation. We have used a mechanostimulatory device to compare characteristics of touch-activated RPDs and action potentials (APs) when cell turgor pressure was changed. The device delivered a series of mechanical stimulations of increasing energy (F0.5, F1, F2, F3, F4, F5 and F6). Cells were alternately stimulated in artificial pondwater (APW) and a sorbitol series, in long-term experiments, involving up to six solution changes. The calculated cell turgor pressures were about 0.6 MPa (APW), and 0.49 MPa, 0.37 MPa, 0.24 MPa and 0.12 MPa in 50, 100, 150 and 200 mM sorbitol–APW, respectively. In other experiments, cells were pre-conditioned in the sorbitol solutions, and then transferred to APW. All cells were allowed long recovery periods (40–60 min) after APs or solution transfers. Only small changes in cell conductance were observed in I–V and G–V analysis of unstimulated cells after reducing turgor pressure from 0.59 MPa to 0.24 MPa. In APW, the RPDs increased in amplitude and duration with increased stimulus energy until the threshold RPD was reached, and an AP was triggered, usually between stimulus F4 and F5. Cells with decreased turgor pressure became more sensitive to stimulation, giving threshold RPDs or APs with smaller stimulus (e.g. between F0.5 and F3). Conversely, an increase in cell turgor pressure (return to APW) led to a decrease in sensitivity to stimulus. When turgor pressure was greatly decreased (to 0.12 MPa), some cells became unresponsive or gave unusual responses. However, only the mechanical part of the touch response was affected by changing the cell turgor pressure. The mean amplitudes of the subthreshold and threshold RPD (that triggers the AP), and of the touch-activated APs, were independent of cell turgor pressure, although action potentials had smaller amplitude when turgor was reduced to about 0.12 MPa. The amplitude of the subthreshold RPD was close to 20 mV, and the amplitude of the threshold RPD was close to 50 mV, in all cells. If tension of the cell wall–plasma membrane–cytoskeleton complex decreased along with decreased cell turgor pressure, a given stimulus could stretch the complex to a greater extent, resulting in activation of more mechanosensory channels. The effect on the RPD of changes in cell turgor pressure is discussed in relation to the mechanical properties of the cell wall–plasma membrane–cytoskeleton complex.

2012 ◽  
Vol 63 (11) ◽  
pp. 4061-4069 ◽  
Author(s):  
B. Lu ◽  
J. Wang ◽  
Y. Zhang ◽  
H. Wang ◽  
J. Liang ◽  
...  

2021 ◽  
Author(s):  
Olivia Muriel ◽  
Laetitia Michon ◽  
Wanda Kukulski ◽  
Sophie G Martin

Cell-cell fusion is central to the process of fertilization for sexual reproduction. This necessitates the remodeling of peri-cellular matrix or cell wall material and the merging of plasma membranes. In walled fission yeast S. pombe, the fusion of P and M cells during sexual reproduction relies on the fusion focus, an actin structure that concentrates glucanase-containing secretory vesicles for local cell wall digestion necessary for membrane fusion. Here, we present a correlative light and electron microscopy (CLEM) quantitative study of a large dataset of 3D tomograms of the fusion site, which revealed the ultrastructure of the fusion focus as an actin-containing, vesicle-dense structure excluding other organelles. Unexpectedly, the data revealed asymmetries between the two gametes: M-cells exhibit a taut and convex plasma membrane that progressively protrudes into P-cells, which exhibit a more slack, wavy plasma membrane. These asymmetries are relaxed upon plasma membrane fusion, with observations of ramified pores that may result from multiple initiations or inhomogeneous expansion. We show that P-cells have a higher exo- to endocytosis ratio than M-cells, and that local reduction in exocytosis abrogates membrane waviness and compromises cell fusion significantly more in P- than M-cells. Reciprocally, reduction of turgor pressure specifically in M-cells prevents their protrusions into P-cells and delays cell fusion. Thus, asymmetric membrane conformations, which result from differential turgor pressure and exocytosis/endocytosis ratios between mating types, favor cell-cell fusion.


2014 ◽  
Vol 104 (9) ◽  
pp. 977-984 ◽  
Author(s):  
Hao-Xun Chang ◽  
Lou Ann Miller ◽  
Glen L. Hartman

Appressoria of some plant-pathogenic fungi accumulate turgor pressure that produces a mechanical force enabling the direct penetration of hyphae through the epidermis. Melanin functions as an impermeable barrier to osmolytes, which allows appressoria to accumulate high turgor pressure. Deficiency of melanin in appressoria reduces turgor pressure and compromises the infection process. In Phakopsora pachyrhizi, the soybean rust pathogen, the appressoria are hyaline. Our objective was to ensure the absence of a melanin layer specifically between the appressorial cell wall and plasma membrane, as well as to determine the turgor pressure of P. pachyrhizi appressoria. We demonstrated that two melanin biosynthesis inhibitors neither reduced turgor pressure nor compromised the infection process. Transmission electron microscopy also showed the absence of a melanin layer between the appressorial cell wall and plasma membrane. In addition, the turgor pressure of P. pachyrhizi appressoria was 5 to 6 MPa, based on extracellular osmolytes used to simulate different osmotic pressures. This is the first report showing that turgor pressure accumulation of P. pachyrhizi appressoria was independent of melanin.


2020 ◽  
Author(s):  
Marc Abella ◽  
Lynnel Andruck ◽  
Gabriele Malengo ◽  
Michal Skruzny

AbstractMechanical forces are integral to many cellular processes, including clathrin-mediated endocytosis, a principal membrane trafficking route into the cell. During endocytosis, forces provided by endocytic proteins and the polymerizing actin cytoskeleton reshape the plasma membrane into a vesicle. Assessing force requirements of endocytic membrane remodelling is essential for understanding endocytosis. Here, we determined forces applied during endocytosis using FRET-based tension sensors integrated into the major force-transmitting protein Sla2 in yeast. We measured force of approx. 10 pN transmitted over Sla2 molecule, hence a total force of 450-1300 pN required for endocytic vesicle formation. Importantly, decreasing cell turgor pressure and plasma membrane tension reduced force requirements of endocytosis. The measurements in hypotonic conditions and mutants lacking BAR-domain membrane scaffolds then showed the limits of the endocytic force-transmitting machinery. Our study provides force values and force profiles critical for understanding the mechanics of endocytosis and potentially other key cellular membrane-remodelling processes.


2014 ◽  
Vol 25 (5) ◽  
pp. 679-687 ◽  
Author(s):  
Roshni Basu ◽  
Emilia Laura Munteanu ◽  
Fred Chang

Yeast and other walled cells possess high internal turgor pressure that allows them to grow and survive in the environment. This turgor pressure, however, may oppose the invagination of the plasma membrane needed for endocytosis. Here we study the effects of turgor pressure on endocytosis in the fission yeast Schizosaccharomyces pombe by time-lapse imaging of individual endocytic sites. Decreasing effective turgor pressure by addition of sorbitol to the media significantly accelerates early steps in the endocytic process before actin assembly and membrane ingression but does not affect the velocity or depth of ingression of the endocytic pit in wild-type cells. Sorbitol also rescues endocytic ingression defects of certain endocytic mutants and of cells treated with a low dose of the actin inhibitor latrunculin A. Endocytosis proceeds after removal of the cell wall, suggesting that the cell wall does not contribute mechanically to this process. These studies suggest that endocytosis is governed by a mechanical balance between local actin-dependent inward forces and opposing forces from high internal turgor pressure on the plasma membrane.


2012 ◽  
Vol 198 (4) ◽  
pp. 637-656 ◽  
Author(s):  
Juan Carlos G. Cortés ◽  
Mamiko Sato ◽  
Javier Muñoz ◽  
M. Belén Moreno ◽  
Jose Angel Clemente-Ramos ◽  
...  

Fungal cytokinesis requires the assembly of a dividing septum wall. In yeast, the septum has to be selectively digested during the critical cell separation process. Fission yeast cell wall α(1-3)glucan is essential, but nothing is known about its localization and function in the cell wall or about cooperation between the α- and β(1-3)glucan synthases Ags1 and Bgs for cell wall and septum assembly. Here, we generate a physiological Ags1-GFP variant and demonstrate a tight colocalization with Bgs1, suggesting a cooperation in the important early steps of septum construction. Moreover, we define the essential functions of α(1-3)glucan in septation and cell separation. We show that α(1-3)glucan is essential for both secondary septum formation and the primary septum structural strength needed to support the physical forces of the cell turgor pressure during cell separation. Consequently, the absence of Ags1 and therefore α(1-3)glucan generates a special and unique side-explosive cell separation due to an instantaneous primary septum tearing caused by the turgor pressure.


2016 ◽  
Vol 80 (3) ◽  
pp. 779-791 ◽  
Author(s):  
Juan C. García Cortés ◽  
Mariona Ramos ◽  
Masako Osumi ◽  
Pilar Pérez ◽  
Juan Carlos Ribas

SUMMARYIn animal cells, cytokinesis requires the formation of a cleavage furrow that divides the cell into two daughter cells. Furrow formation is achieved by constriction of an actomyosin ring that invaginates the plasma membrane. However, fungal cells contain a rigid extracellular cell wall surrounding the plasma membrane; thus, fungal cytokinesis also requires the formation of a special septum wall structure between the dividing cells. The septum biosynthesis must be strictly coordinated with the deposition of new plasma membrane material and actomyosin ring closure and must occur in such a way that no breach in the cell wall occurs at any time. Because of the high turgor pressure in the fungal cell, even a minor local defect might lead to cell lysis and death. Here we review our knowledge of the septum structure in the fission yeastSchizosaccharomyces pombeand of the recent advances in our understanding of the relationship between septum biosynthesis and actomyosin ring constriction and how the two collaborate to build a cross-walled septum able to support the high turgor pressure of the cell. In addition, we discuss the importance of the septum biosynthesis for the steady ingression of the cleavage furrow.


Author(s):  
B.K. Ghosh

Periplasm of bacteria is the space outside the permeability barrier of plasma membrane but enclosed by the cell wall. The contents of this special milieu exterior could be regulated by the plasma membrane from the internal, and by the cell wall from the external environment of the cell. Unlike the gram-negative organism, the presence of this space in gram-positive bacteria is still controversial because it cannot be clearly demonstrated. We have shown the importance of some periplasmic bodies in the secretion of penicillinase from Bacillus licheniformis.In negatively stained specimens prepared by a modified technique (Figs. 1 and 2), periplasmic space (PS) contained two kinds of structures: (i) fibrils (F, 100 Å) running perpendicular to the cell wall from the protoplast and (ii) an array of vesicles of various sizes (V), which seem to have evaginated from the protoplast.


1993 ◽  
Vol 3 (5) ◽  
pp. 637-646 ◽  
Author(s):  
Jian-Kang Zhu ◽  
Jun Shi ◽  
Utpal Singh ◽  
Sarah E. Wyatt ◽  
Ray A. Bressan ◽  
...  

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