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Lipid membranes are an important component of the biological cell. The profound understanding of their structure and functionality, as well as, the influence of various biologically relevant admixtures on their main characteristics is of great importance for research and development in medicine and pharmacology. The effect of sugars on the behaviour of the membrane cell enjoys an ever-increasing interest as they are biologically significant substances. We have studied the influence of the disaccharide sucrose on the physicochemical properties of SOPC (1-stearoyl-2-oleoyl-sn- glycero-3-phosphocholine) lipid system aiming to gain better understanding of the mechanisms of the interaction between both substances. For that purpose, we have used differential scanning calorimetry and Fourier-transform infrared spectroscopy. Our results show that adding sugar up to 300 mM concentration substantially alters the thermodynamic and structural properties of SOPC. The DSC thermograms at heating reveal a general lowering of the SOPC transition temperature T m from gel to liquid crystalline phase (main phase transition, ordered-disordered phase transition) in the presence of sugar. The corresponding peaks are smeared and harder to trace. In agreement with this, a gradual decrease of the enthalpy values up to 300 mM was measured. The IR spectroscopy study provided spectral evidence for two states of hydration of the phosphate groups in the sugar-SOPC model systems suggesting a mechanism of interaction where only part of the phospholipid headgroups are hydrogen bonded to the sugar molecules. The obtained results are in good agreement with various earlier data including results about the bending elasticity moduli, as well as, some theoretical simulations on the sugar-lipid interactions. The current results also reinforce the potential of sucrose to be used as a cell protector against drought at, both, high and low temperatures., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Cdc42, a member of the Rho family of GTP binding proteins, functions in the formation of polarized actin structures, in elongation of cell shape, and in cell signaling. Although genetic mutations previously have not been available in multicellular organisms, studies have attempted to discern Cdc42 functions in organisms, including Drosophila, using dominant active or interfering alleles. Here, for the first time, we examine the functions of Cdc42 in developing tissues using loss-of-function mutations in the Drosophila Cdc42 gene. We find that Cdc42(-) epithelial cells fail to elongate into a columnar cell shape and cannot maintain a monolayered epithelial structure. In contrast to previous studies, we find no requirement for Cdc42 in cell division or in activation of the Jun N-terminal kinase pathway. In addition, Cdc42 function is not required for cytoplasmic actin filament assembly in the nurse cells during oogenesis, although it may facilitate this process. Furthermore, our results indicate that Cdc42 plays a role in intercellular interactions between the germ line and the somatic follicle cells. These results confirm the role of Cdc42 in actin filament assembly and provide new insights into its functions in epithelial morphogenesis and regulating intercellular signaling events., (Copyright 2000 Academic Press.)