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The endoplasmic reticulum (ER) is the reservoir for calcium in cells. Luminal calcium levels are determined by calcium-sensing proteins that trigger calcium dynamics in response to calcium fluctuations. Here we report that Selenoprotein N (SEPN1) is a type II transmembrane protein that senses ER calcium fluctuations by binding this ion through a luminal EF-hand domain. In vitro and in vivo experiments show that via this domain, SEPN1 responds to diminished luminal calcium levels, dynamically changing its oligomeric state and enhancing its redox-dependent interaction with cellular partners, including the ER calcium pump sarcoplasmic/endoplasmic reticulum calcium ATPase (SERCA). Importantly, single amino acid substitutions in the EF-hand domain of SEPN1 identified as clinical variations are shown to impair its calcium-binding and calciumdependent structural changes, suggesting a key role of the EFhand domain in SEPN1 function. In conclusion, SEPN1 is a ER calcium sensor that responds to luminal calcium depletion, changing its oligomeric state and acting as a reductase to refill ER calcium stores.

Involution of the mammary gland after lactation is a dramatic example of coordinated cell death. Weaning causes distension of the alveolar structures due to the accumulation of milk, which, in turn, activates STAT3 and initiates a caspase-independent but lysosome-dependent cell death (LDCD) pathway. Although the importance of STAT3 and LDCD in early mammary involution is well established, it has not been entirely clear how milk stasis activates STAT3. In this report, we demonstrate that protein levels of the PMCA2 calcium pump are significantly downregulated within 2–4 h of experimental milk stasis. Reductions in PMCA2 expression correlate with an increase in cytoplasmic calcium in vivo as measured by multiphoton intravital imaging of GCaMP6f fluorescence. These events occur concomitant with the appearance of nuclear pSTAT3 expression but prior to significant activation of LDCD or its previously implicated mediators such as LIF, IL6, and TGFβ3, all of which appear to be upregulated by increased intracellular calcium. We further demonstrate that increased intracellular calcium activates STAT3 by inducing degradation of its negative regulator, SOCS3. We also observed that milk stasis, loss of PMCA2 expression and increased intracellular calcium levels activate TFEB, an important regulator of lysosome biogenesis through a process involving inhibition of CDK4/6 and cell cycle progression. In summary, these data suggest that intracellular calcium serves as an important proximal biochemical signal linking milk stasis to STAT3 activation, increased lysosomal biogenesis, and lysosome-mediated cell death.

Many stresses are associated with increased accumulation of reactive oxygen species (ROS) and polyamines (PAs). PAs act as ROS scavengers, but export of putrescine and/or PAs to the apoplast and their catabolization by amine oxidases gives rise to H 2 O 2 and other ROS, including hydroxyl radicals (•OH). PA catabolization-based signalling in apoplast is implemented in plant development and programmed cell death and in plant responses to a variety of biotic and abiotic stresses. Central to ROS signalling is the induction of Ca 2+ influx across the plasma membrane. Different ion conductances may be activated, depending on ROS, plant species, and tissue. Both H 2 O 2 and •OH can activate hyperpolarization-activated Ca 2+ -permeable channels. •OH is also able to activate both outward K + current and weakly voltage-dependent conductance (ROSIC), with a variable cation-to-anion selectivity and sensitive to a variety of cation and anion channel blockers. Unexpectedly, PAs potentiated •OH-induced K + efflux in vivo, as well as ROSIC in isolated protoplasts. This synergistic effect is restricted to the mature root zone and is more pronounced in salt-sensitive cultivars compared with salt-tolerant ones. ROS and PAs suppress the activity of some constitutively expressed K + and non-selective cation channels. In addition, both •OH and PAs activate plasma membrane Ca 2+ -ATPase and affect H + pumping. Overall, •OH and PAs may provoke a substantial remodelling of cation and anion conductance at the plasma membrane and affect Ca 2+ signalling.

Four plasma membrane calcium ATPases in Arabidopsis, ACA8, ACA10, ACA12, and ACA13, have overlapping and differential roles in vegetative growth, reproductive development, stomatal movement control, and disease resistance. Abstract Plant cells have multiple plasma membrane (PM)-localized calcium ATPases (ACAs) pumping calcium ions out of the cytosol. Although the involvement of some of these ACAs in plant growth and immunity has been reported, their individual and combined functions have not been fully examined. Here, we analysed the effects of single and combined mutations of four ACA genes, ACA8, ACA10, ACA12, and ACA13, in a number of processes. We found that these four genes had both overlapping and differential involvements in vegetative growth, inflorescence growth, seeds setting, disease resistance and stomatal movement. Disruption of any of these four genes reduces seed setting, indicating their contribution to the overall fitness of the plants. While ACA10 and ACA8 play major roles in vegetative growth and immunity, ACA13 and ACA12 are also involved in these processes especially when the function of ACA10 and/or ACA8 is compromised. The loss of ACA13 and ACA10 function in combination with a reduction in function of ACA8 leads to seedling death at bolting, revealing the essential role of their collective function in plant growth. Taken together, this study indicates a highly tuned calcium system involving these PM-localized calcium pumps in plant growth and environmental responses.

Summary 275 I. Introduction 276 II. Ca²⁺ signalling pathways 276 III. Shaping Ca²⁺ signatures 278 IV. Ca²⁺ influx channels 278 V. Ca²⁺ influx channels as modulators of Ca²⁺ signatures 281 VI. Ca²⁺ efflux transporters 282 VII. Ca²⁺ efflux transporters as modulators of Ca²⁺ signatures 284 VIII. The shaping of noncytosolic Ca²⁺ signatures 285 IX. Future insights into the role of Ca²⁺ oscillators from modelling studies 287 X. Conclusions and perspectives 288 Acknowledgements 288 References 288 In numerous plant signal transduction pathways, Ca²⁺ is a versatile second messenger which controls the activation of many downstream actions in response to various stimuli. There is strong evidence to indicate that information encoded within these stimulus-induced Ca²⁺ oscillations can provide signalling specificity. Such Ca²⁺ signals, or 'Ca²⁺ signatures', are generated in the cytosol, and in noncytosolic locations including the nucleus and chloroplast, through the coordinated action of Ca²⁺ influx and efflux pathways. An increased understanding of the functions and regulation of these various Ca²⁺ transporters has improved our appreciation of the role these transporters play in specifically shaping the Ca²⁺ signatures. Here we review the evidence which indicates that Ca²⁺ channel, Ca²⁺-ATPase and Ca²⁺ exchanger isoforms can indeed modulate specific Ca²⁺ signatures in response to an individual signal.

In this study, the mechanism recruited by exogenous melatonin application at 100 μM for alleviating chilling injury in tomato fruits during cold storage was investigated. Alleviating chilling injury in tomato fruits in response to exogenous melatonin application at 100 μM may ascribe to providing sufficient intracellular ATP occur by higher H-ATPase, Ca-ATPase, cytochrome c oxidase (CCO), and succinate dehydrogenase (SDH) enzymes activity during cold storage. Also, higher unsaturated/saturated fatty acids (unSFA/SFA) ratio owing to higher linoleic and linolenic acids accumulation coincides with lower palmitic, stearic and oleic acids accumulation may be responsible for alleviating chilling injury in tomato fruits in response to exogenous melatonin application at 100 μM, which may occur by higher fatty acid desaturase 3 and 7 ( FAD3 and FAD7) genes expression accompanying by lower phospholipase D (PLD) and lipoxygenase (LOX) genes expression and enzymes activity, in addition to providing sufficient intracellular ATP. Therefore, exogenous melatonin application may be a beneficial postharvest procedure for alleviating chilling injury in tomato fruits during cold storage.

Calcium ions (Ca2+) serve as a crucial signaling mechanism in almost all cells. The buffers are proteins that bind free Ca2+ to reduce the cell’s Ca2+ concentration. The most studies reported in the past on calcium signaling in various cells have considered the buffer concentration as constant in the cell. However, buffers also diffuse and their concentration varies dynamically in the cells. Almost no work has been reported on interdependent calcium and buffer dynamics in the cells. In the present study, a model is proposed for inter-dependent spatio-temporal dynamics of calcium and buffer by coupling reaction–diffusion equations of Ca2+ and buffer in a hepatocyte cell. Boundary and initial conditions are framed based on the physiological state of the cell. The effect of various parameters viz. inositol 1,4,5-triphosphate receptor (IP3R), diffusion coefficient, SERCA pump and ryanodine receptor (RyR) on spatio-temporal dynamics of calcium and buffer regulating diacylglycerol (DAG) in a normal and obese hepatocyte cell has been studied using finite element simulation. From the results, it is concluded that the dynamics of calcium and buffer impact each other significantly along the spatio-temporal dimensions, thereby affecting the regulation of all the processes including DAG in a hepatocyte cell. The proposed model is more realistic than the existing ones, as the interdependent system dynamics of calcium and buffer have different regulatory impacts as compared to the individual and independent dynamics of these signaling processes in a hepatocyte cell.

Presenilin mutations are the main cause of familial Alzheimer's disease (FAD). Presenilins also play a key role in Ca²⁺ homeostasis, and their FAD-linked mutants affect cellular Ca²⁺ handling in several ways. We previously have demonstrated that FAD-linked presenilin 2 (PS2) mutants decrease the Ca²⁺ content of the endoplasmic reticulum (ER) by inhibiting sarcoendoplasmic reticulum Ca²⁺-ATPase (SERCA) activity and increasing ER Ca²⁺ leak. Here we focus on the effect of presenilins on mitochondrial Ca²⁺ dynamics. By using genetically encoded Ca²⁺ indicators specifically targeted to mitochondria (aequorin- and GFP-based probes) in SH-SY5Y cells and primary neuronal cultures, we show that overexpression or down-regulation of PS2, but not of presenilin 1 (PS1), modulates the Ca²⁺ shuttling between ER and mitochondria, with its FAD mutants strongly favoring Ca²⁺ transfer between the two organelles. This effect is not caused by a direct PS2 action on mitochondrial Ca²⁺-uptake machinery but rather by an increased physical interaction between ER and mitochondria that augments the frequency of Ca²⁺ hot spots generated at the cytoplasmic surface of the outer mitochondrial membrane upon stimulation. This PS2 function adds further complexity to the multifaceted nature of presenilins and to their physiological role within the cell. We also discuss the importance of this additional effect of FAD-linked PS2 mutants for the understanding of FAD pathogenesis.

Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) have the potential to remuscularize infarcted hearts but their arrhythmogenicity remains an obstacle to safe transplantation. Myofibroblasts are the predominant cell-type in the infarcted myocardium but their impact on transplanted hiPSC-CMs remains poorly defined. Here, we investigate the effect of myofibroblasts on hiPSC-CMs electrophysiology and Ca 2+ handling using optical mapping of advanced human cell coculture systems mimicking cell–cell interaction modalities. Human myofibroblasts altered the electrophysiology and Ca 2+ handling of hiPSC-CMs and downregulated mRNAs encoding voltage channels (K V 4.3, K V 11.1 and Kir6.2) and SERCA2a calcium pump. Interleukin-6 was elevated in the presence of myofibroblasts and direct stimulation of hiPSC-CMs with exogenous interleukin-6 recapitulated the paracrine effects of myofibroblasts. Blocking interleukin-6 reduced the effects of myofibroblasts only in the absence of physical contact between cell-types. Myofibroblast-specific connexin43 knockdown reduced functional changes in contact cocultures only when combined with interleukin-6 blockade. This provides the first in-depth investigation into how human myofibroblasts modulate hiPSC-CMs function, identifying interleukin-6 and connexin43 as paracrine- and contact-mediators respectively, and highlighting their potential as targets for reducing arrhythmic risk in cardiac cell therapy.

Increased endoplasmic reticulum (ER) stress is one of the central mechanisms that lead to dysregulated metabolic homeostasis in obesity. It is thus crucial to understand the underpinnings of the mechanisms that lead to the development of ER stress. A high level of ER Ca²⁺ is imperative for maintenance of normal ER function and this high Ca²⁺ concentration of ER is maintained by sarco(endo)plasmic reticulum Ca²⁺-ATPase (SERCA). Here, we show that SERCA2b protein and mRNA levels are dramatically reduced in the liver of obese mice and restoration of SERCA2b in the liver of obese and diabetic mice alleviates ER stress, increases glucose tolerance, and significantly reduces the blood glucose levels. Furthermore, overexpression of SERCA2b in the liver of obese mice significantly reduces the lipogenic gene expression and the triglyceride content in the liver. Our results document the importance of SERCA2b in dysregulated glucose and lipid homeostasis in the liver of obese mice and suggest development of drugs to increase SERCA2b activity for treatment of type 2 diabetes and nonalcoholic steatohepatitis.