Alien Registration- Brouillet, Arthur P. (Dresden, Lincoln County)

https://digitalmaine.com/alien_docs/13005/thumbnail.jp

Alien Registration- Brouillet, Arthur P. (Dresden, Lincoln County)

https://digitalmaine.com/alien_docs/13005/thumbnail.jp

Oxysterol and 9-cis-retinoic acid stimulate the group IIA secretory phospholipase A2 gene in rat smooth-muscle cells.

The inflammation that occurs during rheumatoid arthritis or atherosclerosis is characterized by the release of large amounts of sPLA(2) (group IIA secretory phospholipase A(2)). We have shown previously that the sPLA(2) promoter in SMC (smooth-muscle cells) is activated by interleukin-1beta and cAMP-signalling pathways, through the interplay of multiple transcription factors [Antonio, Brouillet, Janvier, Monne, Bereziat, Andreani, and Raymondjean (2002) Biochem. J. 368, 415-424]. In the present study, we have investigated the regulation of sPLA(2) gene expression in rat aortic SMCs by oxysterols. We found that oxysterol ligands that bind to the LXR (liver X receptor), including 25-HC (25-hydroxycholesterol) and 22( R )-HC, cause the accumulation of sPLA(2) mRNA and an increased enzyme activity. Transient transfection experiments demonstrated that the sPLA(2) promoter is synergistically activated by 22( R )-HC in combination with 9- cis -retinoic acid, a ligand for the LXR heterodimeric partner RXR (retinoid X receptor). Promoter activity was also increased in a sterol-responsive fashion when cells were co-transfected with LXRalpha/RXRalpha or LXRbeta/RXRalpha. Mutagenesis studies and gel mobility-shift assays revealed that LXR/RXR heterodimers regulate sPLA(2) transcription directly, by interacting with a degenerated LXRE (LXR response element) at position [-421/-406] of the sPLA(2) promoter. Chromatin immunoprecipitation revealed the in vivo occupancy of LXR on the sPLA(2) promoter. In addition, the orphan nuclear receptor LRH-1 (liver receptor homologue-1) potentiated the sterol-dependent regulation of the sPLA(2) promoter by binding to an identified promoter element (TCAAGGCTG). Finally, we have demonstrated that oxysterols act independent of interleukin-1beta and cAMP pathways to activate the sPLA(2) promoter. In the present study, we have identified a new pathway activating sPLA(2) gene expression in SMCs

Grasping a chestnut burr: Manual laterality in action’s coding strategies

International audienceThis work aimed to assess the role of manual laterality in action coding strategies and, subsequently, in environmental features relevant for each hand's action. Relying on Eder and Hommel's (2013) proposal, we distinguished stimulus-related and end state-related consequences in a Simon paradigm where right-handed participants were divided into two groups, one responding with gloves and one without. Two objects were presented pictorially: one for which sensory consequences of grasping were negatively valenced (a chestnut burr), and one for which they were positively valenced (an apricot). By these means, stimulus and end-state effects could be assessed separately, along with the relevance of each feature of the experimental settings. Results showed that the use of one's dominant or non dominant hand gives rise to different repercussions of stimulus-related and end state-related effects on response: Responses made with the right (dominant) hand were based on an elaborated coding (representing features of stimulus-related and end state-related consequences of action). In contrast, responses made with the left (non dominant) hand seemed to be based on a less elaborated coding (not taking into account end-state consequences of an action)

When the vibrations allow for anticipating the force to be produced: an extend to Pfister et al. (2014)

International audienceAccording to the ideomotor theory, action selection is done by the mental anticipation of its perceptual consequences. If the distal information processed mainly by vision and hearing are considered essential for the representation of the action, the proximal information processed by the sense of touch and proprioception is of less importance. Recent works seem to show the opposite. Nevertheless, it is necessary to complete these results by offering a situation, more ecological, where response and effect can occur on the same effector. So, the goal of our work was to implement a more relevant spatial correspondence because to touch is not the same action that to hear or to see. To do so, participants pressed a specific key after the presentation of a stimulus. The key vibrated depending on the pressure exerted on it. In a compatible condition, high pressure on a key triggered a high vibration, while in an incompatible condition high pressure triggered a low vibration on the same effectors. As expected, the response times were faster in the compatible condition than the incompatible condition. This means that proximal information participates actively in the selection of action

Modeling an enactivist multiple-trace memory. ATHENA: A fractal model of human memory

International audienceGlobal-matching models of memory argue that knowledge emerges from the interaction between presented cues and traces of past experiences. But these models generally rely on the use of independent episodic traces, unable to account for global interactions between learned situations (see Versace et al., 2009). Enactivism (Varela, 1993) could theoretically take advantage of an inter-dependent processing of traces to account for abstraction processing using only sensorimotor covariances (Hutto & Myin, 2012), but no mathematical formalization of an enactivist memory has yet been proposed. In this paper, we propose the ATHENA model as an enactivist mathematical formalization of Act-In theories (Versace et al., 2014) within MINERVA2 (Hintzman, 1986) non-specific traces: ATHENA is a fractal model which keeps track of former processes that led to the emergence of knowledge, and is therefore able to process contextual processes (abstraction manipulation). We present three simulations designed to test ATHENA’s ability to construct, learn, and manipulate emergent abstractions

Transcriptional regulation of the rat type IIA phospholipase A2 gene by cAMP and interleukin-1beta in vascular smooth muscle cells: interplay of the CCAAT/enhancer binding protein (C/EBP), nuclear factor-kappaB and Ets transcription factors.

The abundant secretion of type IIA secreted phospholipase A(2) (sPLA(2)) is a major feature of the inflammatory process of atherosclerosis. sPLA(2) is crucial for the development of inflammation, as it catalyses the production of lipid mediators and induces the proliferation of smooth muscle cells. We have analysed the activation of sPLA(2) transcription by cAMP and interleukin-1beta (IL-1beta), and shown that the 500 bp region upstream of the transcription start site of the rat sPLA(2) gene is implicated in activation by synergistically acting cAMP and IL-1beta. We transiently transfected and stimulated rat smooth muscle cells in primary culture and measured the promoter activities of serial and site-directed deletion mutants of sPLA(2)-luciferase constructs. A distal region, between -488 and -157 bp, bearing a CAAT/enhancer binding protein (C/EBP)-responsive element (-242 to -223) was sufficient for cAMP/protein kinase A-mediated sPLA(2) promoter activation. We find evidence for the first time that activation of the sPLA(2) promoter by IL-1beta requires activation of an Ets-responsive element in the -184 to -180 region of the distal promoter via the Ras pathway and a nuclear factor-kappaB site at positions -141 to -131 of the proximal promoter. We also used electrophoretic mobility shift assays to identify five binding sites for the Sp1 factor; a specific inhibitor of Sp1, mithramycin A, showed that this factor is crucial for the basal activity of the sPLA(2) promoter