Impacts of climate variations on non-stationarity of streamflow over Canada.

With climate change, understanding and assessing the impact of climate variations on non-stationary changes of streamflow is of importance in the hydrologic and atmospheric sciences. In this study, tempo-spatial and scaling effects in the impacts of 18 climate variations on nonstationary streamflow for 279 watersheds across Canada are explored. Specifically, the change point and trends of streamflow are examined through Pettitt's test and Mann-Kendall test. Spatial patterns of correlations between the climate variations and flow rates over Canada, especially their non-stationarity, are investigated at seasonal and decadal scales. The patterns are also quantified by seven spatial classification algorithms under method uncertainty. A series of findings regarding the impacts are revealed. For instance, nonstationary changes of streamflow exist for approximately 9% of Canadian watersheds and most of them are located in Prairie Provinces and the eastern coast. The Atlantic Multidecadal Oscillation, Niño 12, Niño 3, Niño 4, and Niño 3.4 pose significant impacts on Canadian streamflow, which vary with watersheds and seasons. The impacts are closely associated with human activities, e.g., significant impacts of climate variations on populated-area streamflow over Canada. Different climatic variations have different time-varying effects on streamflow. All watersheds have obvious clustering characteristics and four spatial patterns are identified, which is insensitive with classification algorithm. These findings are conducive to understanding the hydrological impacts of atmospheric circulation and enhancing the reliability of hydrological prediction.

Correction to: CDK5 Regulates PD-L1 Expression and Cell Maturation in Dendritic Cells of CRSwNP.

The article CDK5 Regulates PD-L1 Expression and Cell Maturation in Dendritic Cells of CRSwNP, written by C. C. Liu, H. L. Zhang, L. L. Zhi, P. Jin, L. Zhao, T. Li, X. M. Zhou, D. S. Sun, G. H. Cheng, Q. Xin, L. Shi, and M. Xia was originally published electronically on the publisher's internet.

CDK5 Regulates PD-L1 Expression and Cell Maturation in Dendritic Cells of CRSwNP.

The maturation of dendritic cells is critical for chronic rhinosinusitis with nasal polyps (CRSwNPs), especially eosinophilic chronic rhinosinusitis with nasal polyps (EosCRSwNPs), but the regulation mechanism of dendritic cells (DCs) maturation is still unclear. We identified nasal mucosa of 20 patients with EosCRSwNP, 16 non-EosCRSwNP patients, and inferior turbinate of 14 patients with nasal septum deviation after surgery. The expression of cyclin-dependent kinase 5 (CDK5) and programmed cell death 1 ligand 1 (PD-L1) were detected by immunofluorescent, real-time quantitative PCR, and Western blot in EosCRSwNP. The level of dendritic cell maturation was detected by flow cytometry and immunofluorescence staining after CDK5 expression interference with small interfering RNA (siRNA). The expression of CDK5 and PD-L1 in EosCRSwNP nasal mucosal tissue was significantly higher than that of non-EosCRSwNP and inferior turbinate nasal mucosa tissue, and there was a positive correlation between them. Immunofluorescence staining showed that CDK5 and PD-L1 were co-localized in dendritic cells. Synergistic stimulation of dendritic cells with LPS and TNF-α promotes the maturation of dendritic cells and increases the expression of CDK5 and PD-L1. However, blocking the expression of CDK5 in dendritic cells with siRNAs leads to a blockage of cell maturation. CDK5 can regulate the expression of PD-L1, and its presence is critical for the maturation of dendritic cells. CDK5 may play an important role in the pathogenesis of CRSwNP disease.

Effects of freeze-thawing cycles on desorption behaviors of PAH-contaminated soil in the presence of a biosurfactant: a case study in western Canada.

Many regions in Canada are facing increasing environmental threats posed by oil and gas exploitation and transportation. These contaminated lands are inevitably subjected to seasonal and diurnal freeze-thawing cycles (FTCs). However, knowledge about the effect of FTCs on the behaviours of hydrophobic contaminants during the aging process of soil is limited. This study investigated the desorption characteristics of phenanthrene in aging soils in the presence of the biosurfactant rhamnolipid under diurnal and seasonal FTC treatments. It was found that the presence of rhamnolipid in soil during the aging process was able to increase the desorption efficiency of phenanthrene. In the presence of rhamnolipid above 100 mg L-1, FTCs could inhibit the sequestration of phenanthrene. Soil moisture and rhamnolipid concentration are two major factors affecting this effect. High moisture content and FTC frequency could lead to lower desorption in the early stage of FTCs due to the increased specific surface area. The sequestration of phenanthrene was less effectively hindered under seasonal FTCs than diurnal FTCs. The results from this study have important implications for understanding the role of surfactants in cold-region soil aging, and for the improvement of site remediation strategies of PAH contaminated soil in cold regions.

Single cell transcriptome profiling revealed differences in gene expression during oocyte maturation in Haimen white goats.

Juvenile in vitro embryo transfer is an important animal reproductive technology that can shorten the generation interval of livestock, explore the reproductive potential of dams with excellent genetic traits, accelerate genetic progress and production efficiency of the herd, and provide a wealth of genetic resources for livestock breeding. However, oocytes from kids do not develop as well as those from female goats during in vitro maturation. To identify differences during different stages of oocyte maturation, we used single cell transcriptome sequencing to compare gene expression in mature oocytes from kids and female goats. We identified 1086 differentially expressed genes in mature oocytes from kids and female goats. Of these, we observed upregulated expression in 355 genes and downregulated expression in 435 genes. The differentially expressed genes were involved in a total of 245 different pathways; of which 30 were significant (P ≤ 0.05). We used real-time quantitative polymerase chain reaction to screen and verify the expression of five genes specifically involved in oocyte maturation (MOS, RPS6KA1, CPEB1, ANAPC13, and CDK1). Further study of these genes will be of great importance for improving the reproductive performance of Haimen white goats.

Proteomic analysis identifies differentially expressed proteins participating in forming Type III brush hair in Yangtze River Delta white goat.

The Yangtze River Delta white goat is a goat breed that can produce high quality brush hair (Type III hair) around the world. This study aimed to compare Type III hair and non-Type III hair goat skin tissues using differentially expressed proteins based on 2-dimensional gel electrophoresis technology. The differentially expressed protein spots were analyzed using the PDquest 8.0 software. Ten protein spots were detected as positive for mass spectrometric analysis based on a threshold of 2-fold change. Through matching based on Ultraflex III TOF/TOF and MASCOT database, four differentially expressed proteins were identified. Fibrinogen beta chain isoform 1 and ATP synthase beta subunit were upregulated in Type III hair, while succinyl-CoA:3-ketoacid-coenzyme A transferase 1-mitochondrial-like and actin-cytoplasmic 1 were upregulated in non-Type III hair. The 4 proteins play important roles in different aspects of hair follicle development. These findings could pave a good foundation for explaining the mechanism of forming Type III hair.

Effects of an enriched environment on myelin sheaths in the white matter of rats during normal aging: A stereological study.

We found that an enriched environment (EE) could delay the loss of myelinated fibers in the white matter of rats during normal aging. However, the reasons for the protective effects of EE on the myelinated fibers were unclear. In this present study, via the use of stereological methods, we quantitatively investigated the myelin sheaths and the axons of myelinated fibers in the white matter of rats reared in an EE or a standard environment (SE) during the aging process. The results showed that an EE induced significant increases in the lengths of myelinated fibers, the axon volumes and the myelin sheath volumes of aging rats when compared with SE rats and that the enrichment effects, with the exception of the axon volumes, were sex- and age-independent. The mean diameter of the myelinated fibers, the mean perimeter of the myelin sheaths and the mean thicknesses of the myelin sheaths were not significantly changed. The EE-induced increase in myelinated fibers was mostly observed in those of smaller diameter (<1µm) with thinner myelin sheaths (<0.16µm), which had an optimal axon-fiber ratio (g=0.61). Our results suggest that EE-induced an increase in myelinated fibers in the white matter of aging rats primarily due to marked remyelination and some ongoing myelination.

Intestinal distribution and fecundity of two species of Diplostomum parasites in definitive hosts.

This paper investigated the intestinal distribution and fecundity of 2 species of Diplostomum parasites, D. spathaceum and D. pseudospathaceum, in 2 species of definitive hosts, herring gull (Larus argentatus) and common gull (L. canus), using both empirical field data and experimental infections. At the level of individual hosts, the parasite species occupied different parts within the intestine, but the fecundity of the worms, measured as the number of eggs in the uterus, did not differ between the parasite species except in wild common gulls. Interestingly, egg numbers in individual hosts were positively correlated between the parasite species suggesting that some birds provided better resources for the parasite species. At the host population level, fecundity of the worms did not differ between the host species or between adult birds and chicks. Both parasite species were also aggregated to the same host individuals and it is likely that aggregation is transferred to gulls from fish intermediate hosts. Individual differences in suitability and parasite numbers between hosts provide important grounds and implications for epidemiological model-based parasite prevention strategies.

Within-lake dynamics in the similarity of parasite assemblages of perch (Perca fluviatilis).

Although parasite communities have been studied extensively in recent years, spatial and temporal variation in factors affecting the communities has received less attention. This paper examined the similarity of parasite assemblages of perch (Perca fluviatilis) in 18 locations within a single lake in relation to geographical distance and temporal dynamics in the host and parasite populations. We expected that in the present study-scale where distinct but potentially interacting host subpopulations could occur, similarity of the assemblages could be affected by seasonal dynamics in host movements particularly during the spawning period. Parasite species showed differences in infection levels between the sampling locations and similarity of the assemblages of autogenic parasite species in winter, measured inversely as difference in parasite numbers, was negatively affected by geographical distance between the locations. However, no such relationship was observed in the allogenic species Ichthyocotylurus variegata. Furthermore, no relationship was found either in autogenic parasites when the locations were re-sampled in summer, after the spawning period of perch. We concluded that the effect of geographical distance on the similarity of parasite assemblages is a dynamic process, which is affected by seasonal dynamics in host and parasite populations.

Effect of anti-digoxin antiserum on endoxin and membrane ATPase activity in hypoxia-reoxygenation induced myocardial injury.

AIM: To evaluate the protective effect of anti-digoxin antiserum on hypoxia-reoxygenation induced injured myocardium and its mechanism. METHODS: Anti-digoxin antiserum of different concentrations was used, its effect on endoxin and ATPase activity in cell membrane in hypoxia-reoxygenation myocardium model was observed. RESULTS: The level of endoxin was remarkably higher, ATPase activities in cell membrane were remarkably lower in hypoxic group and hypoxia-reoxygenation injury group than those of normal group; anti-digoxin antiserum could resume ATPase activity in a concentration-dependent manner. CONCLUSION: Rise of endoxin was the molecular biological basis of myocardial damage during myocardial hypoxia-reoxygenation. Anti-digoxin antiserum had lessened myocardial injury and had a protective effect on hypoxia-reoxygenation myocardium by antagonizing effect of endoxin.

Different 3'-end processing produces two independently regulated mRNAs from a single H1 histone gene.

We describe the isolation of a mouse H1 histone gene that encodes two mRNA transcripts. One mRNA ends just beyond the coding region, near a highly conserved palindrome sequence typical of cell cycle-regulated histone genes. The level of this transcript is coupled to DNA replication. The second mRNA ends nearly 1 kilobase downstream near a polyadenylation signal. This mRNA is polyadenylylated, and its accumulation is not coupled to DNA replication. The two mRNAs are regulated independently and in some circumstances in opposite directions under several physiological conditions. The production of a polyadenylylated mRNA from an otherwise cell cycle-regulated histone gene may allow for continued synthesis of the histone protein when DNA synthesis ceases in nondividing cells.

Rapid induction of polyadenylated H1 histone mRNAs in mouse erythroleukemia cells is regulated by c-myc.

Chemically induced differentiation of murine erythroleukemia cells is a multistep process involving a precommitment period in which exposure to inducer leads to cells that are irreversibly committed to terminal differentiation. Certain changes in the expression of cellular proto-oncogenes are an important feature of the precommitment phase. We have identified two H1 histone genes that are rapidly induced during this period. Unlike most histone genes, these two H1 genes encode polyadenylated mRNAs with long 3' untranslated regions. To investigate the relationship between induction of the H1 mRNAs and changes in proto-oncogene expression, we studied two independent series of mouse erythroleukemia cell lines that are inhibited from differentiating because of deregulated expression of transfected copies of c-myc or c-myb. The results showed that induction of the H1 mRNAs was negatively regulated by c-myc. The two H1 histone genes are among the first examples of specific cellular genes that are regulated by c-myc. The timing of their induction suggests that they may play an important role in achieving commitment to terminal differentiation.

Transfection of mouse erythroleukemia cells with myc sequences changes the rate of induced commitment to differentiate.

We have examined the role of the c-myc protooncogene in chemically induced differentiation of mouse erythroleukemia (MEL) cells by transfecting the cells with recombinant plasmids in which c-myc coding sequences were cloned downstream from the mouse metallothionein I promoter in sense and antisense orientations. We previously showed that treatment of MEL cells with inducers of differentiation leads to a rapid (less than 2 hr) decrease in the level of c-myc mRNA. c-myc mRNA is then transiently restored to pretreatment levels approximately 12-18 hr later. These events occur prior to the detection of cells that are irreversibly committed to erythroid differentiation. MEL cell transfectants containing the plasmid with myc in the sense orientation express a chimeric MT-myc mRNA, which also decreases shortly after addition of inducer. However, these clones reexpress myc RNA more rapidly than the parental line and they also differentiate more rapidly. On the other hand, transfectants containing the plasmid with myc in the antisense orientation exhibited a delay in the reexpression of c-myc mRNA and were found to differentiate more slowly than parental cells. Thus, we find a correlation between the time at which myc RNA is reexpressed following inducer treatment and the rate of entry of cells into the terminal differentiation program.