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The molecular and cellular identity of peripheral osmoreceptors
Authors:Lechner Stefan G  Markworth Sören  Poole Kate  Smith Ewan St John  Lapatsina Liudmilla  Frahm Silke  May Marcus  Pischke Sven  Suzuki Makoto  Ibañez-Tallon Inés  Luft Friedrich C  Jordan Jens  Lewin Gary R
Affiliation:1. Department of Neuroscience, Max-Delbrück Center for Molecular Medicine, Robert-Rössle-Straße 10, D-13092 Berlin-Buch, Germany;2. Institute for Clinical Pharmacology, Medical School Hannover, Carl-Neuberg-Straße 1, D-30625 Hannover, Germany;3. Department of Gastroenterology, Hepatology and Endocrinology, Medical School Hannover, Carl-Neuberg-Straße 1, D-30625 Hannover, Germany;4. Department of Pharmacology, Jichi Medical School, 3311-1 Yakushiji, Minamikawachi, Tochigi 329-0498, Japan;5. Experimental and Clinical Research Center (ECRC), Charité Campus Buch, Lindenberger Weg 80, D-13125 Berlin, Germany;6. Charité - Universitätsmedizin Berlin, Charitéplatz 1, 030 45050 Berlin, Germany
Abstract:In mammals, the osmolality of the extracellular fluid (ECF) is highly stable despite radical changes in salt/water intake and excretion. Afferent systems are required to detect hypo- or hyperosmotic shifts in the ECF to trigger homeostatic control of osmolality. In humans, a pressor reflex is triggered by simply drinking water which may be mediated by peripheral osmoreceptors. Here, we identified afferent neurons in the thoracic dorsal root ganglia (DRG) of mice that innervate hepatic blood vessels and detect physiological hypo-osmotic shifts in blood osmolality. Hepatic sensory neurons are equipped with an inward current that faithfully transduces graded changes in osmolality within the physiological range (~15 mOsm). In mice lacking the osmotically activated ion channel, TRPV4, hepatic sensory neurons no longer exhibit osmosensitive inward currents and activation of peripheral osmoreceptors in vivo is abolished. We have thus identified a new population of sensory neurons that transduce ongoing changes in hepatic osmolality.
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