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Jouhanneau, J.-S.

Publications and source records attributed to Jouhanneau, J.-S..

2 recordsLinked to original sources

A specialized cold sensing system in the naked mole-rat

Avoiding cold or seeking warmth are universal animal needs. Homeothermic mammals maintain a constant body temperature despite fluctuating ambient temperatures. One exception is the naked mole-rat which lacks effective thermogenesis. We show that the naked mole-rat has evolved a greatly expanded cold sensing system. Compared to mice, this species has many more cold-sensitive sensory neurons and most express the cold-activated TRPM8 channel. The naked mole-rat TrpM8 gene harbors a unique upstream exon that when translated produces a TRPM8 protein with a 71 amino acid N-terminal extension. When expressed, the N-terminal extension prevents membrane targeting and abolishes TRPM8 function. Splice forms lacking the extension formed functional cold and menthol activated channels in vivo. Additionally, many naked mole-rat sensory neurons use a TRPM8-independent mechanism to detect cold. Thus, we identified molecular changes that confer both sensitivity and flexibility to cold sensing in a species that is critically dependent on following thermal cues.

neuroscience↗

Multiple two-photon targeted whole-cell patch-clamp recordings from monosynaptically connected neurons in vivo

Although we know a great deal about monosynaptic connectivity, transmission and integration in the mammalian nervous system from in vitro studies, very little is known in vivo. This is partly because it is technically difficult to evoke action potentials and simultaneously record small amplitude subthreshold responses in closely (< 150 m) located pairs of neurons. To address this, we have developed in vivo two-photon targeted multiple (2 - 4) whole-cell patch clamp recordings of nearby neurons in superficial layers 1 to 3 of primary somatosensory cortex. Here we describe a step-by-step guide to this approach in the anesthetised mouse, including: the design of the setup, surgery, preparation of pipettes, targeting and acquisition of multiple whole-cell recordings, as well as in vivo and post-hoc histology. The procedure takes ~ 4 hours from start of surgery to end of recording and allows examinations both into the electrophysiological features of unitary excitatory and inhibitory monosynaptic inputs and the synaptic mechanisms of correlated neuronal activity.

neuroscience↗