scholarly journals Ether anesthetics prevents touch-induced trigger hair calcium-electrical signals excite the Venus flytrap

2021 ◽  
Author(s):  
Soenke Scherzer ◽  
Shouguang Huang ◽  
Anda Iosip ◽  
Ines Fuchs ◽  
Ken Yokawa ◽  
...  

Plants do not have neurons but operate transmembrane ion channels and can get electrical excited by physical and chemical clues. Among them the Venus flytrap is characterized by its peculiar hapto-electric signaling. When insects collide with trigger hairs emerging the trap inner surface, the mechanical stimulus within the mechanosensory organ is translated into a calcium signal and an action potential (AP). Here we asked how the Ca2+ wave and AP is initiated in the trigger hair and how it is feed into systemic trap calcium-electrical networks. When Dionaea muscipula trigger hairs matures and develop hapto-electric excitability the mechanosensitive anion channel DmMSL10/FLYC1 and voltage dependent SKOR type Shaker K+ channel are expressed in the sheering stress sensitive podium. The podium of the trigger hair is interface to the flytrap`s prey capture and processing networks. In the excitable state touch stimulation of the trigger hair evokes a rise in the podium Ca2+ first and before the calcium signal together with an action potential travel all over the trap surface. In search for podium ion channels and pumps mediating touch induced Ca2+ transients, we, in mature trigger hairs firing fast Ca2+ signals and APs, found OSCA1.7 and GLR3.6 type Ca2+ channels and ACA2/10 Ca2+ pumps specifically expressed in the podium. Like trigger hair stimulation, glutamate application to the trap directly evoked a propagating Ca2+ and electrical event. Given that anesthetics affect K+ channels and glutamate receptors in the animal system we exposed flytraps to an ether atmosphere. As result propagation of touch and glutamate induced Ca2+ and AP long-distance signaling got suppressed, while the trap completely recovered excitability when ether was replaced by fresh air. In line with ether targeting a calcium channel addressing a Ca2+ activated anion channel the AP amplitude declined before the electrical signal ceased completely. Ether in the mechanosensory organ did neither prevent the touch induction of a calcium signal nor this post stimulus decay. This finding indicates that ether prevents the touch activated, glr3.6 expressing base of the trigger hair to excite the capture organ.

2021 ◽  
Author(s):  
Sönke Scherzer ◽  
Shouguang Huang ◽  
Anda Iosip ◽  
Ines Fuchs ◽  
Ken Yokawa ◽  
...  

Abstract Plants do not have neurons. Instead they operate transmembrane ion channels and can be electrically excited by physical and chemical clues. The Venus flytrap with its distinctive hapto-electric signaling is a prime example. When an insect collides with the trigger hairs emerging from the inner surface of the trap, the mechanical stimulus in the mechanosensory organ is translated into a calcium signal and an action potential (AP). Here we asked how a Ca 2+ wave and AP are initiated in the trigger hair and how these are fed into the systemic trap calcium-electric network. When the Dionaea muscipula trigger hair matures and develops hapto-electric excitability, the mechanosensitive anion channel DmMSL10 and voltage dependent SKOR type Shaker K + channel are expressed in the shear stress-sensitive podium, which interfaces with the flytrap’s prey capture and processing networks. In the excitable state, touch stimulation of the trigger hair first evokes a rise in the podium Ca 2+ , then the calcium signal together with an action potential, travel over the entire trap surface. Seeking the mechanisms that mediate touch-induced Ca 2+ transients in the mature trigger hairs, we show that OSCA1.7 and GLR3.6 type Ca 2+ channels and ACA2/10 Ca 2+ pumps are specifically expressed in the podium. In addition, we found that direct glutamate application to the trap evoked a propagating Ca 2+ and electrical event. Given that anesthetics affect K + channels and glutamate receptors in animal systems, we exposed flytraps to ether. An ether atmosphere suppressed the propagation of touch and glutamate-induced Ca 2+ and AP long-distance signaling, a response that was completely recovered when ether was replaced by fresh air. In line with ether targeting a calcium channel, so triggering a Ca 2+ activated anion channel, the AP amplitude declined before the electrical signal ceased completely. Ether in the mechanosensory organ neither prevented the touch induction of a calcium signal nor its post stimulus decay. This finding indicates that ether prevents the touch activated GLR3.6-expressing base of the trigger hair so exciting the capture organ.


Plants ◽  
2020 ◽  
Vol 9 (5) ◽  
pp. 587 ◽  
Author(s):  
Takuma Hagihara ◽  
Masatsugu Toyota

As sessile organisms, plants do not possess the nerves and muscles that facilitate movement in most animals. However, several plant species can move quickly in response to various stimuli (e.g., touch). One such plant species, Mimosa pudica L., possesses the motor organ pulvinus at the junction of the leaflet-rachilla, rachilla-petiole, and petiole-stem, and upon mechanical stimulation, this organ immediately closes the leaflets and moves the petiole. Previous electrophysiological studies have demonstrated that a long-distance and rapid electrical signal propagates through M. pudica in response to mechanical stimulation. Furthermore, the spatial and temporal patterns of the action potential in the pulvinar motor cells were found to be closely correlated with rapid movements. In this review, we summarize findings from past research and discuss the mechanisms underlying long-distance signal transduction in M. pudica. We also propose a model in which the action potential, followed by water flux (i.e., a loss of turgor pressure) in the pulvinar motor cells is a critical step to enable rapid movement.


BIOspektrum ◽  
2021 ◽  
Vol 27 (6) ◽  
pp. 601-603
Author(s):  
Michael M. Wudick

AbstractBeing sessile, plants are exposed to adverse stresses, including wounding by insects. Albeit lacking experimental evidence, one hypothesis predicted involvement of hydro-electric signals in wound signaling. Now, we could show that the mechanosensitive anion channel MSL10 is necessary for wound-induced long-distance signaling in plants. By linking mechano-sensing, ion fluxes, membrane depolarization and electrical signal propagation, MSL10 might integrate hydraulic and electric wound signals.


Plants ◽  
2021 ◽  
Vol 10 (2) ◽  
pp. 372
Author(s):  
Ekaterina Sukhova ◽  
Elena Akinchits ◽  
Sergey V. Gudkov ◽  
Roman Y. Pishchalnikov ◽  
Vladimir Vodeneev ◽  
...  

Variation potential (VP) is an important long-distance electrical signal in higher plants that is induced by local damages, influences numerous physiological processes, and participates in plant adaptation to stressors. The transmission of increased hydraulic pressure through xylem vessels is the probable mechanism of VP propagation in plants; however, the rates of the pressure transmission and VP propagation can strongly vary. We analyzed this problem on the basis of a simple mathematical model of the pressure distribution along a xylem vessel, which was approximated by a tube with a pressure gradient. It is assumed that the VP is initiated if the integral over pressure is more than a threshold one, taking into account that the pressure is transiently increased in the initial point of the tube and is kept constant in the terminal point. It was shown that this simple model can well describe the parameters of VP propagation in higher plants, including the increase in time before VP initiation and the decrease in the rate of VP propagation with an increase in the distance from the zone of damage. Considering three types of the pressure dynamics, our model predicts that the velocity of VP propagation can be stimulated by an increase in the length of a plant shoot and also depends on pressure dynamics in the damaged zone. Our results theoretically support the hypothesis about the impact of pressure variations in xylem vessels on VP propagation.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Anne Fabricant ◽  
Geoffrey Z. Iwata ◽  
Sönke Scherzer ◽  
Lykourgos Bougas ◽  
Katharina Rolfs ◽  
...  

AbstractUpon stimulation, plants elicit electrical signals that can travel within a cellular network analogous to the animal nervous system. It is well-known that in the human brain, voltage changes in certain regions result from concerted electrical activity which, in the form of action potentials (APs), travels within nerve-cell arrays. Electro- and magnetophysiological techniques like electroencephalography, magnetoencephalography, and magnetic resonance imaging are used to record this activity and to diagnose disorders. Here we demonstrate that APs in a multicellular plant system produce measurable magnetic fields. Using atomic optically pumped magnetometers, biomagnetism associated with electrical activity in the carnivorous Venus flytrap, Dionaea muscipula, was recorded. Action potentials were induced by heat stimulation and detected both electrically and magnetically. Furthermore, the thermal properties of ion channels underlying the AP were studied. Beyond proof of principle, our findings pave the way to understanding the molecular basis of biomagnetism in living plants. In the future, magnetometry may be used to study long-distance electrical signaling in a variety of plant species, and to develop noninvasive diagnostics of plant stress and disease.


2021 ◽  
Vol 72 (1) ◽  
pp. 75-83
Author(s):  
Zoltan Varga ◽  
Gabor Tajti ◽  
Gyorgy Panyi

AbstractSince the discovery of the Kv1.3 voltage-gated K+ channel in human T cells in 1984, ion channels are considered crucial elements of the signal transduction machinery in the immune system. Our knowledge about Kv1.3 and its inhibitors is outstanding, motivated by their potential application in autoimmune diseases mediated by Kv1.3 overexpressing effector memory T cells (e.g., Multiple Sclerosis). High affinity Kv1.3 inhibitors are either small organic molecules (e.g., Pap-1) or peptides isolated from venomous animals. To date, the highest affinity Kv1.3 inhibitors with the best Kv1.3 selectivity are the engineered analogues of the sea anemone peptide ShK (e.g., ShK-186), the engineered scorpion toxin HsTx1[R14A] and the natural scorpion toxin Vm24. These peptides inhibit Kv1.3 in picomolar concentrations and are several thousand-fold selective for Kv1.3 over other biologically critical ion channels. Despite the significant progress in the field of Kv1.3 molecular pharmacology several progressive questions remain to be elucidated and discussed here. These include the conjugation of the peptides to carriers to increase the residency time of the peptides in the circulation (e.g., PEGylation and engineering the peptides into antibodies), use of rational drug design to create novel peptide inhibitors and understanding the potential off-target effects of Kv1.3 inhibition.


Circulation ◽  
2020 ◽  
Vol 142 (Suppl_3) ◽  
Author(s):  
Junjun Li ◽  
Itsunari Minami ◽  
Shigeru Miyagawa ◽  
Xiang Qu ◽  
YING HUA ◽  
...  

Introduction: How to precisely evaluate response in newly developed medications in vitro may be a great concern in drug screening. We modified normal low-attachment culture dish and created closed-loop tissue ring from single hiPSC-CMs. We hypothesized that the re-entrant wave (ReW) could originate and pace the cardiac tissue ring, and the CMs under pacing could be matured and used for drug assessment. Methods: PDMS wells and pillars were mounted in low-attachment petri dishes (Figure 1A). 4 х 10 5 hiPSC-CMs were plated into the wells to form tissue ring where the ReW could spontaneously originate. After cultivation for 14 days, the hiPSC-CMs were evaluated by immunostaining and gene expression. Micro electrode array (MEA) were used to evaluating the CM response to different drugs. Results: The electrical signal recorded by MEA indicated that the ReWs could make the CMs beat at a much higher rate than the Control group (Figure 1B, 123.26 ± 10.36 bpm vs. 14.08 ± 4.53 bpm, p<0.0001). After 14 day culture, the ReW group demonstrated significantly higher expression of Troponin T (TnT2), myosin heavy chain 7 (β-MHC), and α-actinin. Interestingly, the α-actinin staining indicated alignment of CMs within the ReW group (Figure 1C). The CMs under ReW pacing showed robust response to several cardiac compounds including E4031, (hERG K+ channel blocker, Figure 1D and E), isoproterenol (β adrenoceptor agonist) and propranolol (beta-blocker). Both the field potential as well as the Ca 2+ transients showed correlated dose-dependent change and the recovering after washout of the drugs. Conclusions: The ReWs could spontaneously originate in the cultured cardiac tissue ring with enhancement of the maturation in the hiPSC-CMs and robust response to various drugs, indicating the system as a robust drug assessment system with multiple read-out methods.


Author(s):  
Rose Ellen Dixon ◽  
Manuel F. Navedo ◽  
Marc D Binder ◽  
L. Fernando Santana

Ion channels play a central role in the regulation of nearly every cellular process. Dating back to the classic 1952 Hodgkin-Huxley model of the generation of the action potential, ion channels have always been thought of as independent agents. A myriad of recent experimental findings exploiting advances in electrophysiology, structural biology, and imaging techniques, however, have posed a serious challenge to this long-held axiom as several classes of ion channels appear to open and close in a coordinated, cooperative manner. Ion channel cooperativity ranges from variable-sized oligomeric cooperative gating in voltage-gated, dihydropyridine-sensitive Cav1.2 and Cav1.3 channels to obligatory dimeric assembly and gating of voltage-gated Nav1.5 channels. Potassium channels, transient receptor potential channels, hyperpolarization cyclic nucleotide-activated channels, ryanodine receptors (RyRs), and inositol trisphosphate receptors (IP3Rs) have also been shown to gate cooperatively. The implications of cooperative gating of these ion channels range from fine tuning excitation-contraction coupling in muscle cells to regulating cardiac function and vascular tone, to modulation of action potential and conduction velocity in neurons and cardiac cells, and to control of pace-making activity in the heart. In this review, we discuss the mechanisms leading to cooperative gating of ion channels, their physiological consequences and how alterations in cooperative gating of ion channels may induce a range of clinically significant pathologies.


Science ◽  
1961 ◽  
Vol 133 (3456) ◽  
pp. 878-879 ◽  
Author(s):  
J. R. Di Palma ◽  
R. Mohl ◽  
W. Best

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