Biogeohemical significance of Intracellular calcification by Cyanobacteria

Author(s):  
Neha Mehta ◽  
Feriel-Skouri Panet ◽  
Karim Benzerara

<p>Cyanobacteria are an abundant and diverse group of photosynthetic bacteria that have shaped Earth’s environment for billions of years and play a vital role in the cycling of numerous elements such as carbon, calcium, and phosphorus. In particular, their impact on the global carbon cycle is of significant interest in the context of carbon capture and climate change, as they sequester atmospheric CO<sub>2</sub> into organic carbon and biogenic calcium carbonates (CaCO<sub>3</sub>) through a process called calcification.  The process of calcification has long been considered as extracellular and non-biologically controlled. However, recently, several cyanobacterial species have been reported to form intracellular amorphous calcium carbonate (ACC) inclusions. These cyanobacteria were found in diverse environments and accumulate high concentrations of AEE (Ca, Ba and Sr) from solutions undersaturated with respect to AEE-carbonate phases. Moreover, one of these cyanobacteria species, <em>G. lithophora</em> was shown to selectively accumulate stable and radioactive alkaline earth elements (AEE) within the intracellular amorphous carbonates and/or polyp inclusions (Mehta et al., 2019). Recently, it was confirmed that cyanobacteria forming intracellular ACC contained a much higher content of alkaline earth elements (AEE) than all other cyanobacteria (DeWever et al., 2019). The high concentration of Ba and Sr within these intracellular inclusions was surprising because Ba and Sr have usually been considered as having no physiological role at all. The high concentration of Ca within these intracellular inclusions was directly in contrast with the traditional paradigm of cells maintaining a state of homeostasis with respect to Ca. Furthermore, Sr/Ca and Ba/Ca ratios in these ACC inclusions were very different from those expected from abiotic precipitation in the solution surrounding the cells (Cam et al. 2015). To understand the biological driver behind these observations, first, I will present a review of the above mentioned “vital effects” in the context of intracellular calcification in cyanobacteria. Second, using batch incubation experiments, I will show that high Ca concentrations are vital not only for the growth of <em>G. lithophora</em>, but also for the uptake of Ba by <em>G. lithophora</em>. Lastly, I will examine Ca homeostasis in ACC forming cyanobacterial strains by using an antagonist/inhibitor of a known channel/transporter involved in Ca transport.  Overall, these insights will shed some light on the role of cyanobacteria forming intracellular ACC on carbonate (bio)mineralization, in both modern and ancient Earth’s environment. </p><p>Reference:</p><p>N Mehta, K Benzerara, B Kocar, V Chapon, Sequestration of radionuclidesRadium-226 and Strontium-90 by cyanobacteria forming intracellular calcium carbonates, ES&T 2019</p><p>De Wever, A.; Benzerara, K. et al. Evidence of High Ca Uptake by Cyanobacteria Forming Intracellular CaCO 3 and Impact on Their Growth. Geobiology 2019</p><p>Cam, N., Georgelin, T., Jaber, M., Lambert, J.-F., and Benzerara, K, In vitro synthesis of amorphous Mg-, Ca-, Sr- and Ba-carbonates: what do we learn about intracellular calcification by cyanobacteria? Geochim. Cosmochim. Acta 2015</p><p> </p>

1984 ◽  
Vol 100 (2) ◽  
pp. 219-226 ◽  
Author(s):  
S. A. Nicholson ◽  
T. E. Adrian ◽  
B. Gillham ◽  
M. T. Jones ◽  
S. R. Bloom

ABSTRACT The effect of six hypothalamic peptides on the basal release of ACTH and that induced by arginine vasopressin (AVP) or by ovine corticotrophin releasing factor (oCRF) from fragments of the rat anterior pituitary gland incubated in vitro was investigated. Dose–response curves to AVP and to oCRF were obtained, and the response to a low dose of oCRF was potentiated by a low dose of AVP. Basal release of ACTH was not affected by any of the peptides in concentrations in the range 10−12 to 10−6 mol/l, and only substance P (SP) and somatostatin (SRIF) inhibited significantly the response to oCRF in a dose-related manner. The responses to a range of doses of oCRF or AVP were reduced by 10−8 and 10 − 6 mol SP or SRIF/1, and to a greater extent by the higher dose. Except in the case of 10−6 mol SRIF/1 on the response to AVP, the response was not further diminished by preincubation of the tissue with the peptide before the stimulating agent was added. The inhibition of the responses to AVP or oCRF by 10−9 mol SP/1 was not potentiated by its combination with either 5 × 10−10 or 10−8 mol SRIF/1; the inhibitory effects were merely additive. The results suggest that although SRIF and SP are able to modulate the release of ACTH from the anterior pituitary gland, they do so only at a high concentration. In the case of SRIF these concentrations are several orders of magnitude higher than those reported to be present in the hypophysial portal blood and therefore a physiological role for this peptide in the control of ACTH secretion is unlikely. J. Endocr. (1984) 100, 219–226


2012 ◽  
Vol 22 (4) ◽  
pp. 249-258 ◽  
Author(s):  
Cláudia N. Santos ◽  
Marta M. Alves ◽  
Isabel T. Bento ◽  
Ricardo B. Ferreira

AbstractDuring the maturation of dicotyledonous seeds, organic carbon, nitrogen and sulphur are stored in protein storage vacuoles (PSVs) as storage globulins. Several studies point to the coexistence of storage proteins with proteases responsible for their degradation inside PSVs. Different mechanisms have been proposed to explain why there is no proteolysis during this period. Protein aggregation to form large supramolecular structures resistant to proteolytic attack could be the reason. However, during germination, and particularly following its completion, the globulin aggregates must undergo disintegration to allow protease attack for protein reserve mobilization. Based on the well-described concentration-dependent ability of Ca2+ and Mg2+ to promote in vitro aggregation and disaggregation of globulins, we explored a possible role for these alkaline earth cations in globulin packaging and mobilization. Ca2+ and Mg2+ measurements in purified PSVs [6.37 μmol and 43.9 μmol g− 1 dry weight (DW) of cotyledons, respectively] showed the presence of these two alkaline earth cations within this compartment. To our knowledge, this is the first time that Ca2+ and Mg2+ have been quantified in purified PSVs from Lupinus albus seeds. Considering the importance of these two alkaline earth cations inside PSVs, which represent 14.6% and 60.7% of the total seed Mg2+and Ca2+, respectively, globulin aggregation and disaggregation profiles were assayed using experimental conditions closer to those that are physiologically present (proportion of Ca2+ and Mg2+, and acidic pH). Based on: (1) the high in vivo abundance of Ca2+ and Mg2+ inside PSVs; and (2) globulin aggregation and disaggregation profiles, together with structural and physiological evidence already reported in the literature, an important physiological role for Ca2+ and Mg2+ in globulin packaging and mobilization inside PSVs is suggested.


2020 ◽  
Vol 26 (1) ◽  
pp. 2137-2142
Author(s):  
A. M. Meskatul ◽  
K. Shimasaki ◽  
S. U. Habiba

Different types of bio-polysaccharide play a vital role in the growth of PLBs cultured in vitro. In this study, to we investigated the potential impacts of two bio-polymers,: hyaluronic acid (HA9) and sodium alginate (ALG) on the organogenesis of protocorm-like bodies (PLBs) in Phalaenopsis under white LED lights. PLBs of Phalaenopsis ‘Fmk02010’ were explanted on modified MS medium with different concentrations of HA and (ALG). The highest average number of PLBs per explant (24.6) was recorded for ALG alone at a concentration of 0.01mg/L, and the fresh weight was also highest at the same concentration. The combination of 0.01mg/L ALG and 0.01mg/L HA also resulted in a large number of PLBs (23.8) and high fresh weight. As opposed to, the highest number of shoots /explant (3.6) was observed at the treatment of the combination of 1mg/L ALG and 10mg/L HA. This study shows that the application of ALG and HA alone, and in combination, at low concentrations, increased the average number of PLBs and the amount of fresh weight, but shoot formation was higher at a high concentration compared with control.


1988 ◽  
Vol 34 (10) ◽  
pp. 2044-2047 ◽  
Author(s):  
P Gallice ◽  
J P Monti ◽  
M Baz ◽  
A Murisasco ◽  
A Crevat

Abstract An in vitro inhibitor of Na+/K+-transporting ATPase (EC 3.6.1.37) was isolated from uremic plasma and normal urine by liquid chromatography. A 23Na nuclear magnetic resonance study involving living erythrocytes showed that this inhibitor causes impairment of the Na+-K+ pump of intact erythrocytes. This finding may explain the high intra-erythrocytic sodium concentration in those uremic patients exhibiting a high concentration of this inhibitor. The presence of this same inhibitor in normal urine suggests that it may play a physiological role.


Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 264
Author(s):  
Francesca Cestari ◽  
Francesca Agostinacchio ◽  
Anna Galotta ◽  
Giovanni Chemello ◽  
Antonella Motta ◽  
...  

Biogenic calcium carbonates naturally contain ions that can be beneficial for bone regeneration and therefore are attractive resources for the production of bioactive calcium phosphates. In the present work, cuttlefish bones, mussel shells, chicken eggshells and bioinspired amorphous calcium carbonate were used to synthesize hydroxyapatite nano-powders which were consolidated into cylindrical pellets by uniaxial pressing and sintering 800–1100 °C. Mineralogical, structural and chemical composition were studied by SEM, XRD, inductively coupled plasma/optical emission spectroscopy (ICP/OES). The results show that the phase composition of the sintered materials depends on the Ca/P molar ratio and on the specific CaCO3 source, very likely associated with the presence of some doping elements like Mg2+ in eggshell and Sr2+ in cuttlebone. Different CaCO3 sources also resulted in variable densification and sintering temperature. Preliminary in vitro tests were carried out (by the LDH assay) and they did not reveal any cytotoxic effects, while good cell adhesion and proliferation was observed at day 1, 3 and 5 after seeding through confocal microscopy. Among the different tested materials, those derived from eggshells and sintered at 900 °C promoted the best cell adhesion pattern, while those from cuttlebone and amorphous calcium carbonate showed round-shaped cells and poorer cell-to-cell interconnection.


2021 ◽  
Author(s):  
Caroline Vance ◽  
Shaakir Salam ◽  
Sara Tacconelli ◽  
Bradley Smith ◽  
Jacqueline Mitchell ◽  
...  

Abstract Aberrantly expressed fused in sarcoma (FUS) is a hallmark of FUS-related amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Wildtype FUS localises to synapses and interacts with mitochondrial proteins while mutations have been shown to cause to pathological changes affecting mitochondria, synapses and the neuromuscular junction (NMJ). This indicates a crucial physiological role for FUS in regulating synaptic and mitochondrial function that is currently poorly understood. In this paper we provide evidence that mislocalised cytoplasmic FUS causes mitochondrial and synaptic changes and that FUS plays a vital role in maintaining neuronal health in vitro and in vivo. Overexpressing mutant FUS altered synaptic numbers and neuronal complexity in both primary neurons and zebrafish models. The degree to which FUS was mislocalised led to differences in the synaptic changes which was mirrored by changes in mitochondrial numbers and transport. Furthermore, we showed that FUS interacts with the mitochondrial tethering protein Syntaphilin (SNPH), and that mutations in FUS affect this relationship. Finally, we demonstrated mutant FUS led to changes in global protein translation. This interaction between FUS and SNPH could explain the synaptic and mitochondrial defects observed leading to global protein translation defects. Importantly, our results support the ‘gain-of-function’ hypothesis for disease pathogenesis in FUS-related ALS.


CrystEngComm ◽  
2011 ◽  
Vol 13 (12) ◽  
pp. 3975 ◽  
Author(s):  
Chantel C. Tester ◽  
Ryan E. Brock ◽  
Ching-Hsuan Wu ◽  
Minna R. Krejci ◽  
Steven Weigand ◽  
...  

2018 ◽  
Author(s):  
Marco Spinazzi ◽  
Enrico Radaelli ◽  
Katrien Horré ◽  
Amaia M. Arranz ◽  
Natalia Gounko ◽  
...  

ABSTRACTThe mitochondrial intramembrane rhomboid protease Parl has been implicated in diverse functions in vitro, but its physiological role in vivo remains unclear. Here we show that Parl ablation in mouse causes a striking necrotizing encephalomyelopathy similar to Leigh syndrome, a mitochondrial disease characterized by disrupted energy production. Mice with conditional Parl deficiency in the nervous system, but not in muscle, develop a similar phenotype as germline Parl knockouts demonstrating the vital role of Parl in neurological homeostasis. Genetic modification of two major Parl substrates, Pink1 and Pgam5, do not modify this severe neurological phenotype. Parl-/- brain mitochondria are affected by defects in Complex III activity and in coenzyme Q biosynthesis. Parl is necessary for the stable expression of Ttc19, required for Complex III activity, and of Coq4, essential in coenzyme Q biosynthesis. Thus, Parl plays a previously overseen constitutive role in the maintenance of the respiratory chain in the nervous system, and its deficiency causes progressive mitochondrial dysfunction and Leigh-like syndrome.


2021 ◽  
Author(s):  
Caroline Vance ◽  
Shaakir Salam ◽  
Sara Tacconelli ◽  
Bradley N Smith ◽  
Jacqueline C Mitchell ◽  
...  

Abstract BackgroundAberrantly expressed fused in sarcoma (FUS) is a hallmark of FUS-related amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Wildtype FUS localises to synapses and interacts with mitochondrial proteins while mutations have been shown to cause to pathological changes affecting mitochondria, synapses and the neuromuscular junction (NMJ) This indicates a crucial physiological role for FUS in regulating synaptic and mitochondrial function that is currently poorly understood.MethodsNeurite complexity and synaptic density were studied in rat primary neurons expressing eGFP-FUSWT, eGFP-FUSR514G or eGFP-FUSΔNLS. To investigate synaptic and neuronal changes in vivo, a motor neuron specific zebrafish over-expression model with mosaic expression of MNX1:Gal4 and UAS: eGFP-FUSWT, UAS: eGFP-FUSR514G or UAS: eGFP-FUSΔNLS was assessed for alterations to axonal growth, branching and NMJ density. Using live imaging, mitochondrial trafficking in in vitro neuronal models expressing mutant FUS was conducted. Complementary proximity ligation assays assessed endogenous protein interactions, while overexpression of mutant FUS evaluated if mutations led to alterations in this interaction. Lastly, Puromycin assays investigated how mutant FUS caused differences in global protein translation. ResultsWe found that mutant FUS alters synaptic numbers and neuronal complexity in both primary neurons and zebrafish models. The degree to which FUS is mislocalised leads to differences in the synaptic changes which is mirrored by changes in mitochondrial numbers and transport. Furthermore, we showed that FUS interacts and localises with Syntaphilin (SNPH), and that mutations in FUS affect this relationship, which may lead to the synaptic and mitochondrial phenotypes observed. Finally, we demonstrated that in primary neurons mutant FUS-driven changes in global protein translation correlate with synaptic and mitochondrial defects shown for each respective mutation. ConclusionsWe provide evidence that mislocalised cytoplasmic FUS causes mitochondrial and synaptic changes and that FUS plays a vital role in maintaining neuronal health in vitro and in vivo. Moreover, we demonstrate a novel interaction between FUS and SNPH, which could explain the synaptic and mitochondrial defects observed leading to global protein translation defects. Importantly, our results support the ‘gain-of-function’ hypothesis for disease pathogenesis in FUS-related ALS.


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