Using lateral substitution to control conformational preference and phase behaviour of benzanilide-based liquid crystal dimers

Open access via the Wiley Agreement Funder: National Science Centre. Grant Number: 2021/43/B/ST5/00240 Acknowledgments D.P. gratefully acknowledges financial support from the National Science Centre (Poland) under the grant no. 2021/43/B/ST5/00240.Peer reviewedPublisher PD

Ferroelectric nematogens containing a methylthio group.

The synthesis and characterisation of eight nematogens containing a terminal methylthio group is reported. The compounds are based on RM734 and differ in the number and position of fluorine substituents, and in the position of the lateral methoxy substituent. Seven of these compounds exhibit a monotropic ferroelectric nematic phase, NF, including examples of NF-isotropic phase transitions. Two of the compounds show the anti-ferroelectric NX phase. Their transitional behaviour is discussed in terms of molecular shape and changes in electronic properties. Their phase behaviour is similar to that of the corresponding compounds containing a terminal methoxy group, but the methoxy terminated materials consistently show the higher transition temperatures. This is accounted for by the larger reduction in molecular shape anisotropy associated with the methylthio group, and the associated change in the electronic properties. The NX phase seen for the methylthio substituted compounds are thought to reflect the suppression of the NF phase by the methylthio group rather than any specific stabilising effect. Specific interactions between methylthio groups thought to stabilise nematic behaviour do not appear to stabilise the NF phase

The Influence of the Imine Bond Direction on the Phase Behaviour of Symmetric and Non-symmetric Liquid Crystal Dimers

Acknowledgements D. P. gratefully thanks the National Science Centre (Poland) under the grant no. 2021/43/B/ST5/00240.Peer reviewedPublisher PD

To be or not to be polar: the ferroelectric and antiferroelectric nematic phases.

We report two new series of compounds that show the ferroelectric nematic, NF, phase in which the terminal chain length is varied. The longer the terminal chain, the weaker the dipole–dipole interactions of the molecules are along the director and thus the lower the temperature at which the axially polar NF phase is formed. For homologues of intermediate chain lengths, between the non-polar and ferroelectric nematic phases, a wide temperature range nematic phase emerges with antiferroelectric character. The size of the antiparallel ferroelectric domains critically increases upon transition to the NF phase. In dielectric studies, both collective ("ferroelectric") and non-collective fluctuations are present, and the "ferroelectric" mode softens weakly at the N–NX phase transition because the polar order in this phase is weak. The transition to the NF phase is characterized by a much stronger lowering of the mode relaxation frequency and an increase in its strength, and a typical critical behavior is observed

Phytosulfokine stimulates cell divisions in sugar beet (Beta vulgaris L.) mesophyll protoplast cultures

The aim of this work was to improve plating efficiency of sugar beet mesophyll protoplast cultures. Preliminary experiments showed that cultures of good quality, viable protoplasts were obtained in rich media based on the Kao and Michayluk formulation and with the calcium alginate as an embedding matrix. Nevertheless, in these cultures cell divisions were either not observed or very seldom confirming earlier reported recalcitrance of sugar beet protoplasts. The recalcitrant status of these cultures was reversed upon application of exogenous phytosulfokine (PSK)—a peptidyl plant growth factor. The highest effectiveness of PSK was observed at 100 nM concentration. Plating efficiencies obtained in the presence of PSK reached approximately 20% of the total cultured cells. The stimulatory effect of phytosulfokine was observed for all tested breeding stocks of sugar beet. Our data indicate that PSK is a powerful agent able to overcome recalcitrance of plant protoplast cultures

JAK2-mutant hematopoietic cells display metabolic alterations that can be targeted to treat myeloproliferative neoplasms

Increased energy requirement and metabolic reprogramming are hallmarks of cancer cells. We show that metabolic alterations in hematopoietic cells are fundamental to the pathogenesis of mutant JAK2-driven myeloproliferative neoplasms (MPNs). We found that expression of mutant JAK2 augmented and subverted metabolic activity of MPN cells, resulting in systemic metabolic changes in vivo, including hypoglycemia, adipose tissue atrophy, and early mortality. Hypoglycemia in MPN mouse models correlated with hyperactive erythropoiesis and was due to a combination of elevated glycolysis and increased oxidative phosphorylation. Modulating nutrient supply through high-fat diet improved survival, whereas high-glucose diet augmented the MPN phenotype. Transcriptomic and metabolomic analyses identified numerous metabolic nodes in JAK2-mutant hematopoietic stem and progenitor cells that were altered in comparison with wild-type controls. We studied the consequences of elevated levels of Pfkfb3, a key regulatory enzyme of glycolysis, and found that pharmacological inhibition of Pfkfb3 with the small molecule 3PO reversed hypoglycemia and reduced hematopoietic manifestations of MPNs. These effects were additive with the JAK1/2 inhibitor ruxolitinib in vivo and in vitro. Inhibition of glycolysis by 3PO altered the redox homeostasis, leading to accumulation of reactive oxygen species and augmented apoptosis rate. Our findings reveal the contribution of metabolic alterations to the pathogenesis of MPNs and suggest that metabolic dependencies of mutant cells represent vulnerabilities that can be targeted for treating MPNs

The effects of alkylthio chains on the properties of symmetric liquid crystal dimers

Open Access via the RSC Agreement Funding Information: D. P. acknowledges funding from the National Science Centre (Poland) under the grant no. 2021/43/B/ST5/00240.Peer reviewedPublisher PD