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SUMMARY Afferent responses to the fish's own electric organ discharge were explored in the electrosensory lobe of the mormyrid fish Gnathonemus petersii. In order to understand the neural encoding of natural sensory images,responses were examined while objects of different conductivities were placed at different positions along the skin of the fish, i.e. at different points within, and also outside, peripheral receptive fields. The presence of an object in the fish's self-generated electric field produces local modulation of transcutaneous current density. Measurement of the local electric organ discharge shows that object images formed at the electroreceptive sensory surface have an opposing center-surround, `Mexican hat' profile. This is a pre-receptor phenomenon intrinsic to the physical nature of the sensory stimulus that takes place prior to neural lateral inhibition and is independent of such central inhibition. Stimulus intensity is encoded in the latency and number of action potentials in the response of primary afferent fibers. It is also reflected in changes in the amplitude and area of extracellular field potentials recorded in the deep granular layer of the electrosensory lobe. Since the object image consists of a redistribution of current density over the receptive surface,its presence is coded by change in the activity of receptors over an area much larger than the skin surface facing the object. We conclude that each receptor encodes information coming from the whole scene in a manner that may seem ambiguous when seen from a single point and that, in order to extract specific object features, the brain must process the electric image represented over the whole sensory surface.

International audience; TFIID, composed of the TATA box binding protein (TBP) and 13 TBP-associated factors (TAFs), plays a role in nucleating the assembly of the RNA polymerase II preinitiation complexes on protein coding genes. TAF10 (formerly TAF(II)30) is shared between TFIID and other transcription regulatory complexes (i.e. SAGA, TFTC, STAGA and PCAF/GCN5). TAF10 is an essential transcription factor during very early stages of mouse embryo development. To study the in vivo function of TAF10 in cellular differentiation and proliferation at later stages, the role of TAF10 was analysed in keratinocytes during skin development and adult epidermal homeostasis. We demonstrate that ablation of TAF10 in keratinocytes of the forming epidermis affects the expression of some, but not all genes, impairs keratinocyte terminal differentiation and alters skin permeability barrier functions. In contrast, loss of TAF10 in keratinocytes of adult epidermis did not (i) modify the expression of tested genes, (ii) affect epidermal homeostasis and (iii) impair acute response to UV irradiation or skin regeneration after wounding. Thus, this study demonstrates for the first time a differential in vivo requirement for a mammalian TAF for the regulation of gene expression depending on the cellular environment and developmental stage of the cell.

International audience; Lateral shifts in overt attention have been previously shown to modulate reaction times to lateral electrocutaneous stimuli, as well as perception or unpleasantness thresholds. A response bias can play a role in the elicitation of these lateral differences. Therefore, the present experiment aimed at investigating whether eye orientation induces a decision bias in favour of the ipsilateral hemispace. Participants were asked whether or not they suspected subliminal electrocutaneous shocks, whereas no subliminal stimulation was actually delivered. A secondary visual task led participants to direct their eyes ipsi- or contralateral to the stimulated area. Differences between experimental conditions in the amount of subliminal shocks participants acknowledge to receive (number of positive responses) are thought to reflect decision biases. Low and high trait anxiety participants were involved. Results showed an interaction between the eye orientation and the tested hand. The number of positive responses was smaller in right-hand tests with contralateral eye orienting. This effect fits those described previously with real electrocutaneous stimuli. This interaction is related to hemispheric differences in spatial attention. In contrast to thresholds studies, this study failed to replicate that a lateral difference arises in the low but not in the high trait anxiety individuals, suggesting that this interaction was mostly due to the neurosensory processing of the electrocutaneous stimuli.

Modulation of non-monosynaptic excitation from ankle dorsiflexors to quadriceps (Q) motoneurones during human treadmill walking was investigated in 25 healthy human subjects. Stimulation of the common peroneal nerve (CPN) evoked a biphasic facilitation in the rectified and averaged (n = 50) Q electromyographic (EMG) activity between 0 and 100 ms after heel strike. Prior to heel strike, the stimulation had no effect on the Q EMG. The latency of both peaks in the response was too long to be explained by a monosynaptic pathway to Q motoneurones. During voluntary tonic co-contraction of Q and tibialis anterior (TA) while standing, only the first of the two peaks was evoked by the CPN stimulation despite a background EMG activity level in the Q and TA muscles corresponding to that observed 30-60 ms after heel strike during walking. Stimulation of cutaneous nerves did not evoke a similar biphasic facilitation in the Q motoneurones, which suggests that muscular afferents mediate the response. The second peak had a higher threshold than the earlier peak. During cooling of the CPN, the latency of the second peak was more prolonged than the latency of the earlier peak. This suggests that afferents of different diameters contributed to the two peaks. It is proposed that afferents from TA assist the contraction of Q during walking via spinal interneurones to stabilize the knee joint and maintain upright posture during walking.

International audience; Reaction time to expected lateral cutaneous stimulation was measured in Man when the eyes were directed (1) towards the stimulated area, (2) towards another point within the same hemispace and (3) towards the other hemispace. As performance was better in the first case, this suggests that compatible eye postural activity reinforces the effect of spatial attention.

The Hoffmann (H) reflex and its facilitation produced by electrical stimulation of the sural area were examined before a ballistic extension of the right foot. Modulations of the cutaneous facilitation of the H reflex (CFH) were used to assess the control exerted over the transmission of low threshold cutaneous afferents. The time-course of H and CFH changes were investigated at the end of the foreperiod and during the premotor period, i.e. between the response signal and the onset of the electromyogram (EMG) of the soleus muscle. Four stimulation conditions were set up depending on whether the H reflex was elicited on the contracting or non-contracting limb, and whether cutaneous stimulation was ipsilateral or contralateral to the reflex. During the 100 ms preceding the response signal, the inhibition of the H reflex was more marked in the contracting limb than in the noncontracting limb. At the end of the foreperiod, the CFHs had a symmetric time course: the CFHs evoked by conditioning stimulation of the contracting limb were facilitated just before the response signal, while those produced by conditioning stimulation to the non-contracting limb were depressed. It is suggested that these variations are related to postural adjustments taking place before the movement is performed. As previously reported, the H reflex of the contracting limb exhibited a marked increase in amplitude over the 50 ms preceding the EMG. Reflex facilitations showed specific variations according to the ankle stimulated and the soleus muscle tested. The CFHs produced by stimulation of the non-contracting limb regained, at the end of the premotor period, a value close to their reference level recorded in trials without movement. The CFHs, produced by conditioning stimulation of the contracting limb were modulated differently according to whether the tested soleus muscle was contracting or not: when the CFH was tested on the contracting muscle, it was found to be depressed throughout the premotor period; this contrasted significantly with the isolated depression recorded on the non-contracting muscle. Therefore, only the cutaneous afferents from the mobilized limb, modulating the H reflex of the same limb, were subject to a specific inhibition during the premotor period. Throughout the preparatory and premotor periods, negative correlations were observed between H and CFH amplitude, except just before the EMG onset in the condition where the H reflex was delivered to the contracting muscle and the cutaneous stimulation to the ankle of the non-contracting limb: in this case, CFH amplitude increase paralleled that of the reflex amplitude. The negative correlations between these two variables are discussed in terms of a central control regulating the balance between proprioceptive and cutaneous input.