Dopamine system genes associated with parenting in the context of daily hassles

The current study examined the molecular genetic foundations of sensitive parenting in humans and is the first to test the interaction between genes and environment in modulating parental sensitive responses to children. In a community sample of 176 Caucasian, middle class mothers with their 23-month-old toddlers at risk for externalizing behavior problems, the association between daily hassles and sensitive parenting was investigated. We tested whether two dopamine-related genes, dopamine D4 receptor ( DRD4 ) and catechol-O-methyltransferase ( COMT ) gene polymorphisms, modulate parents' vulnerability to the negative influence of daily hassles on sensitive parenting behavior to their offspring. Sensitive parenting was observed in structured settings, and parents reported on their daily hassles through a standard questionnaire. In parents with the combination of genes leading to the least efficient dopaminergic system functioning ( COMT val/val or val/met, DRD4 -7Repeat), more daily hassles were associated with less sensitive parenting, and lower levels of daily hassles were associated with more sensitive parenting d  = 1.12. The other combinations of COMT and DRD4 polymorphisms did not show significant associations between daily hassles and maternal sensitivity, suggesting differential susceptibility to hassles depending on parents' dopaminergic system genes. It is concluded that the study of (multiple) gene–environment interactions (in the current case: gene by gene by environment interaction, G × G × E) may explain why some parents are more and others less impacted by daily stresses in responding sensitively to their offspring's signals.     

Life history strategies and psychopathology: the faster the life strategies,the more symptoms of psychopathology

There is little extant empirical literature examining the associations between life history strategies and symptoms of psychopathology. The current study (N = 138) investigated the associations between life history strategies, symptoms of psychopathology, aggression, incidence of self-harm behaviour, and attachment (perceived parental support) in sample drawn from the general population and community mental health service providers. The results from the study indicate those with a faster life strategy report greater levels of aggression and symptoms of psychopathology. Further, perceptions of poorer parental support were associated with a faster life history strategy. Implications for life history theory, conceptualising psychopathology, and future research directions are discussed.     

登革热Ⅱ型病毒受体的初步研究

本实验用甲基纤维素复盖层的c_6/36单层细胞微量蚀斑法的间接免疫荧光法,初步观察了登革热Ⅱ型病毒与靶细胞的联接反应情况。同时还制备了四种细胞的可溶性膜制剂,并研究了它们对登革热Ⅱ型病毒的抑制活性。结果提示,对登革热Ⅱ型病毒敏感的细胞表面存在登革热Ⅱ型病毒受体,在触发病毒感染阶段起重要作用。     

Differential specificity of substrate-attached lectins stimulating spreading of GH3-cells under serum-free,hormone-supplemented culture conditions

Summary Most mammalian cells are capable of growth in culture only when they are supplied with an appropriate substrate to which they can adhere and spread. To prepare suitable substrates different lectins were attached onto polystyrene tissue-culture dishes after coating with polylysine. GH₃-cells (a pituitary-tumor-cell line) were seeded into the culture dishes containing serumfree, hormone-supplemented medium. When succinylated Concanavalin A (s-ConA), which binds specifically to mannose residues, is attached to the surface an extraordinary spreading of GH₃-cells is induced within 15 to 20 min after seeding. Other lectins with a different sugar-binding specificity are less effective in inducing cell spreading. However, the cell spreading depends not only on the substrate-attached lectins but also on the hormones used in the proliferation-culture of GH₃-cells. Both types of molecules found in the microenvironment of a cell, the matrix-fixed sugar-binding proteins and the diffusive hormones, are responsible for the regulation of the behaviour of the mammalian cell. It is suggested that the interaction of the cell-surface carbohydrates with the plasma-membrane-bound lectins of contiguous cells plays a central role in such processes, especially in in-vivo.     

A novel approach to measuring heat flux in swimming animals

We present a design for long-term or removable attachment of heat flux sensors (HFSs) to stationary or swimming animals in water that enables collection of heat flux data on both captive and free-ranging pinnipeds. HFSs were modified to allow for independent, continuous, and long-term or removable attachment to study animals. The design was tested for effects of HFSs and the attachment mechanism on resultant heat flux. Effects were insulative and consistent across water temperatures and flow speeds, resulting in a correction factor of 3.42. This correction factor was applied to all measurements of heat flux from animal experiments to account for the thermal resistance of HFSs and insulative effects of the attachment mechanism. Heat flux and skin temperature data were collected from two captive Steller sea lions (Eumetopias jubatus) as they swam in a large habitat tank over time periods ranging from approximately 4 to 9 min. Of the 72 HFSs deployed using the attachment mechanism, data were successfully retrieved from 70. The HFS attachment mechanism was also used on two wild free-ranging Weddell seals (Leptonychotes weddellii) off Ross Island, Antarctica, for up to 7 days. Heat flux data were retrieved from all eight sensors deployed. These results, along with those from Steller sea lions, suggest that HFSs can be deployed with success on captive and wild animals using the designed attachment mechanism.     

Identification of New Interactions between Endolysosomal Tethering Factors

Proper functioning of the precisely controlled endolysosomal system is essential for maintaining the homeostasis of the entire cell. Tethering factors play pivotal roles in mediating the fusion of different transport vesicles, such as endosomes or autophagosomes with each other or with lysosomes. In this work, we uncover several new interactions between the endolysosomal tethering factors Rabenosyn-5 (Rbsn) and the HOPS and CORVET complexes. We find that Rbsn binds to the HOPS/CORVET complexes mainly via their shared subunit Vps18 and we mapped this interaction to the 773–854 region of Vps18. Based on genetic rescue experiments, the binding between Rbsn and Vps18 is required for endosomal transport and is dispensable for autophagy. Moreover, Vps18 seems to be important for β1 integrin recycling by binding to Rbsn and its known partner Vps45.     

Attachment, ingestion and intracellular killing of Helicobacter pylori by human peripheral blood mononuclear leukocytes and mouse peritoneal inflammatory macrophages

Abstract The different steps of phagocytosis, attachment, ingestion and intracellular killing of cells of Helicobacter pylori strain 17874 (expressing sialic acid-specific haemagglutinin) and cells of H. pylori strain 17875 (expressing non-sialic acid-specific haemagglutinin) have been studied. More cells of sialopositive H. pylori strain 17874 have been found attached to human peripheral blood mononuclear leukocytes (PBM) and mouse peritoneal inflammatory macrophages (PIM) than cells of sialonegative H. pylori strain 17875. Binding of cells of H. pylori strain 17874 has been significantly inhibited by treatment of phagocytes with neuraminidase. Inhibition of adhesion of these bacteria preincubated with foetuin to normal phagocytic cells has also been found. Well adhering cells of H. pylori strain 17874 were more resistant to killing mechanisms of human PBM and mouse PIM than cells of strain 17875. Good, probably sialic acid-specific haemagglutinin dependent, adhesion of H. pylori bacteria to phagocytes can be considered as an important virulence factor which facilitates the pathogen to avoid the defence mechanisms.     

Specific binding of lactoferrin to Aeromonas hydrophila

The subunit S1 of pertussis toxin (PT) was purified as the recombinant product BacS1 from the culture supernatant of a Bacillus subtilis strain containing a secretion vector with a DNA fragment coding for the mature subunit S1 inserted downstream of the signal sequence of the alpha-amylase gene. The method of purification was successive ion exchange and adsorption chromatography. BacS1 occurred in two forms (28 and 20 kDa) of which the truncated 20-kDa peptide was the main one in the supernatant. The truncated BacS1 was purified and shown to have the same NH2-terminus as the full-size (28 kDa) BacS1. It was also enzymatically active indicating correct conformation. The truncated BacS1 was also shown to elicit neutralizing and protective antibodies when injected into mice or rabbits.