Elastic Properties of Confined Fluids in Nanopores: An Acoustic-Propagation Model.

Following the compressibility route in statistical mechanics, the local isothermal modulus is derived for nanoconfined fluids. Based on this inhomogeneous modulus, an acoustic-propagation model (APM) is first proposed for averaged isothermal modulus in the pore. By utilizing the density profiles obtained from classical density functional theory, the inhomogeneous modulus of supercritical methane in the graphite slit pore is calculated. It is found that the profile of the modulus in the pore is out of phase with that of density. Further, employing the proposed APM method, the averaged isothermal modulus is calculated, and the effects of pressure, pore size, and temperature on the averaged modulus are investigated. It is found that (i) averaged modulus obtained from APM method still satisfies the Tait-Murnaghan (TM) equation, (ii) the averaged modulus is proportional to the reciprocal pore width for wider pores, while it oscillates with the reciprocal pore width for narrower pores, and (iii) the reciprocal modulus is proportional to temperature, while the linearization coefficient is insensitive to the pore size. These findings bear important implications for understanding the elasticity in fluid-saturated nanoporous media and may shed light on the capture or storage of special gases in the fields of geochemistry and geophysics.

LncRNA TUG1 Regulates Proliferation of Cardiac Fibroblast via the miR-29b-3p/TGF-ß1 Axis.

Background: Atrial fibrillation (AF) is a very common clinical arrhythmia, accompanied by the overproliferation of cardiac fibroblasts (CFs). This study aimed to investigate the role of the long non-coding RNA(lncRNA) taurine upregulated gene 1 (TUG1) in the proliferation of CFs and further investigated its underlying mechanism. Methods: One hundred four paroxysmal AF patients and 94 healthy controls were recruited. Human cardiac fibroblasts (HCFs) were applied to establish an AF cell model through treatment with angiotensin II (AngII). qRT-PCR was used for the measurement of gene levels. The cell proliferation was detected by cell counting kit-8 (CCK-8). Luciferase reporter assay was performed for target gene analysis. Results: Elevated levels of TUG1 and low expression of miR-29b-3p were detected in the serum of AF patients compared with the healthy controls. Pearson's correlation analysis exhibited an inverse relationship between TUG1 and miR-29b-3p expression in AF patients (r = -7.106, p < 0.001). Knockdown of TUG1 inhibited AngII-induced CF proliferation. Taurine upregulated gene 1 (TUG1) functions as a competing endogenous RNA (ceRNA) for miR-29b-3p, and downregulation of miR-29b-3p reversed the role of TUG1 in CF proliferation. TGF-ß1 is a direct target gene of miR-29b-3p. Conclusions: Long non-coding RNA taurine upregulated gene 1 is a key regulator in the occurrence of AF. Slicing TUG1 inhibits CF proliferation by regulating the miR-29b-3p/TGF-ß1 axis.

Long non-coding RNA SENCR alleviates hypoxia/reoxygenation-induced cardiomyocyte apoptosis and inflammatory response by sponging miR-1.

BACKGROUND: Myocardial cell apoptosis is one of the main reasons for the occurrence of acute myocardial infarction (AMI). The role of smooth muscle and endothelial cell enriched migration/differentiation-associated lncRNA (SENCR) in the cardiomyocyte apoptosis induced by hypoxia/reoxygenation (H/R) injury and its potential mechanism were investigated in this study to provide a novel biomarker for the development of AMI. METHODS: The expression levels of SENCR in the serum of AMI patients and non-AMI patients with chest pain (control) were detected by qRT-PCR. The function of SENCR in the cardiomyocyte apoptosis and inflammatory response induced by H/R injury was evaluated by MTT, cell apoptosis, and ELISA assay, respectively. The mechanism underlying the function of SENCR was investigated with the luciferase reporter assay. RESULTS: SENCR was significantly downregulated in AMI compared with the control volunteers, which showed negative correlations with the cardiac troponin I (cTnI) and creatine kinase-MB (CK-MB) level of patients. The H/R injury-induced cell apoptosis and inflammatory response in cardiomyocytes, which were attenuated by the overexpression of SENCR. The expression of miR-1 was suppressed by the overexpression of SENCR, while the overexpression of miR-1 could alleviate the cell apoptosis, enhance cell viability, and attenuate inflammatory response in cardiomyocyte. SENCR reversed H/R-induced myocardial cell injury by regulating the expression of miR-1. CONCLUSIONS: SENCR was correlated with the clinicopathological features of patients and was revealed to alleviate the cardiomyocyte apoptosis and inflammatory response induced by H/R injury via sponging miR-1.

[Analysis of phenotype and CYP4V2 gene variants in two pedigrees affected with Bietti crystalline corneoretinal dystrophy].

OBJECTIVE: The CYP4V2 gene of two pedigrees affected with Bietti crystalline corneoretinal dystrophy was analyzed to indentify the cause of the disease and provide a basis for clinical diagnosis. METHODS: The probands were subjected to next generation sequencing (NGS). Suspected variants were verified by Sanger sequencing. Pathogenicity of the variants were searched through relevant databases and PubMed by following the ACMG guidelines. RESULTS: A homozygous variant in the CYP4V2 gene c. (802-8) _810delTCATACAGGTCATCGCTinsGC was detected in proband from pedigree 1, parents did not detect; CYP4V2 genes c. (802-8)_810delTCATACAGGTCATCGCTinsGC and c. 958 C>T (p.Arg320X) compound heterozygous variants existed in the proband of pedigree 2,both parents were variant carriers. The results of Sanger sequencing showed that the variant of CYP4V2 gene in the two families was consistent with the NGS sequencing. The c. (802-8)_810delTCATACAGGTCATCGCTinsGC of CYP4V2 gene was splicing variant, and both splicing variant and nonsense variant could produce truncated nonfunctional protein products. Based on standards and guidelines by American College of Medical Genetics and Genomics, the CYP4V2 genes c. (802-8)_810del TCATACAGGTCATCGCTinsGC and c. 958 C>T (p.Arg320X) were predicted to be pathogenic variants (PVS1+PS1+PM2+PM3). CONCLUSION: The homozygous variant c. (802-8) _810delTCATACAGGTCATCGCTinsGC and the complex heterozygous variants c. (802-8) _810delTCATACAGGTCATCGCTinsGC and c.958C>T (p.Arg320X) in CYP4V2 gene are the cause of the disease in the probands of two pedigrees , respectively.

[Clinical characteristics and variant analysis of five pedigrees with hereditary spastic paraplegia].

OBJECTIVE: To explore the clinical and genetic characteristics of five pedigrees affected with hereditary spastic paraplegia(HSP). METHODS: Clinical data of the five pedigrees was collected, and high-throughput sequencing was carried out to detect potential variants. Sanger sequencing were used to verify the results. RESULTS: The probands of pedigree 1 and 2 were found to harbor heterozygous SPAST gene variants, namely c.1196C>T and c.1523T>A. The proband of pedigree 3 harbored compound heterozygous variants of FA2H gene (c.61G>C and c.688G>A). Proband from pedigree 4 harbored compound heterozygous variants of SPG11 gene (c.6812+4_6812+7delAGTA and c.915delT). The proband of pedigree 5 harbored compound heterozygous variants of SPG7 gene (c.1703_1704delAG and c.1937-1G>C). Based on the American College of Medical Genetics and Genomics(ACMG) guidelines, all variants were predicted to be likely pathogenic. Among these, SPAST gene c.1523T>A, FA2H gene c.61.G>C, SPG11 gene splicing region c.6812+4_6812+7delAGTA, c.915delT, SPG7 gene c.1703_1704delAG and splicing region c.1937-1G>C variants were unreported previously. CONCLUSION: The probands of pedigrees 1 and 2 were diagnosed with autosomal dominant hereditary spastic paraplegia type 4, for which pedigree 2 showed incompletely penetrance. Pedigrees 3, 4, and 5 were diagnosed with autosomal recessive hereditary spastic paraplegia type 35, 11 and 7, respectively. Above result provided a reference for clinical diagnosis and genetic counseling for the affected pedigrees.

Pressure Profile for an Associating Lennard-Jones Fluid Confined in a Spherical Cavity.

We present the pressure tensor of an associating Lennard-Jones (LJ) fluid confined in a spherical cavity of hard wall, where a high-order density correlation has been taken into account. To give the two-body association potential for calculating the pressure tensor, an angle-average of site-site attraction over all orientations of two particles is performed. Furthermore, the classical density functional theory is employed to obtain the density profile of the confined fluid, by which the normal and tangential pressure profiles are illustrated under various conditions to show the dependence of the pressure tensor on the association strength, number of associating sites, radius of cavity, and bulk density. As an application, the corresponding surface tension is calculated. It is shown that under a strong association interaction (both association strength and the number of associating sites are large), the pressure profiles are depleted from the wall of the cavity instead of the oscillatory behavior under a weak association interaction. Such a tendency is mainly determined by the competition between association interaction and excluded volume interaction. Therefore, the aggregation state and related properties of an associating LJ fluid within a confinement of nanoscale can be efficiently regulated by the association interaction.

Spontaneous separation of large-spin Fermi gas in the harmonic trap: a density functional study.

The component separation of the trapped large-spin Fermi gas is studied within density functional theory. The ground state and ferromagnetic transition in the gas, with and without the spin mixing collision, are calculated. In the absence of spin mixing, two patterns of separation are observed as the interaction between atoms increases, whereas only one of them corresponds to a ferromagnetic transition. The phase diagram suggests that the pattern which the system chooses depends on the interaction strength in the collision channels. With the presence of spin mixing, the distribution of phase region changes because of the interplay between different collision channels. Specifically, the spin exchange benefits the FM transition, while it suppresses the component separation of CS-II pattern.

Size selectivity in the confined ternary colloidal mixtures: the depletion in the competition.

Based on classical density functional theory, we study the size selectivity for ternary colloidal mixtures in the presence of a Gauss barrier. The competition between the external potential and the depletion potential is also investigated. The effects of bulk fraction of each species, the size asymmetry, and the strength and width of the Gauss barrier on the selectivity of the big species are calculated and analyzed in detail. The results in different conditions of bulk fraction suggest that the larger the bulk fraction for the small species, the stronger selectivity of big particles. On the contrary, increase of bulk fraction for the big species leads to a reduction in selectivity. In addition, results under different conditions of size asymmetry suggest that the medium particles can also be selected by the Gauss barrier when they are sufficiently large in comparison to the small particles. We also demonstrate the effect of barrier geometry on the selectivity of the big species and the competition between the depletion and the external potential.

[Influence of recombined human growth hormone on sIgA and EGF in rats with obstructive jaundice].

AIM: To study the effect of the recombined human growth hormone(rhGH) on secretory immunoglobulin A (sIgA), epidermal growth factor (EGF) in rats with obstructive jaundice. METHODS: Sixty Wistar rats were randomly divided into four groups, sham-operated (group A), common biliary duct-ligated (group B), biliary duct-ligated plus rhGH-treat for one week (group C), biliary duct-ligated plus rhGH-treat for two weeks (group D), each group had 15 rats. Except group A, the rats of other groups were operated with biliary duct-ligated. Until two weeks after operation, the rats of group A and B were killed. After operation, the rats of group C were treated with rhGH hypodermic injection (0.75 U x kg(-1) x d(-1)) for one week, and then killed. The rats of D group were treated with rhGH hypodermic injection (0.75 U x kg(-1) x d(-1)) for two weeks, and then killed. All procedures were performed aseptically. Total bilirubin (TB), alkaline phosphatase (ALP), prealbumin(PA), insulin-like growth factor (IGF-1), sIgA, EGF were measured. RESULTS: Compared with group A, in group B, C, D, serum level of PA, IGF-1 and sIgA, EGF level of gastric and intestinal juice were lower, but TB, ALP were higher, there were significant difference. Compared with group B, the rats with treatment of rhGH in group C and D had higher sIgA and EGF and lower intestinal bacterial translocation. CONCLUSION: In objective jaundice rats, rhGH can protect their hepatic function, intestinal physical-barrier function and immune-barrier function, and reduce intestinal bacterial translocation.