Connexin26 mediates CO2-dependent regulation of breathing via glial cells of the medulla oblongata
Joseph van de Wiel, Louise Meigh, Amol Bhandare, Jonathan Cook, Sarbjit Nijjar, Robert Huckstepp, Nicholas Dale
Abstract
Abstract Breathing is highly sensitive to the PCO 2 of arterial blood. Although CO 2 is detected via the proxy of pH, CO 2 acting directly via Cx26 may also contribute to the regulation of breathing. Here we exploit our knowledge of the structural motif of CO 2 -binding to Cx26 to devise a dominant negative subunit (Cx26 DN ) that removes the CO 2 -sensitivity from endogenously expressed wild type Cx26. Expression of Cx26 DN in glial cells of a circumscribed region of the mouse medulla - the caudal parapyramidal area – reduced the adaptive change in tidal volume and minute ventilation by approximately 30% at 6% inspired CO 2 . As central chemosensors mediate about 70% of the total response to hypercapnia, CO 2 -sensing via Cx26 in the caudal parapyramidal area contributed about 45% of the centrally-mediated ventilatory response to CO 2 . Our data unequivocally link the direct sensing of CO 2 to the chemosensory control of breathing and demonstrates that CO 2 -binding to Cx26 is a key transduction step in this fundamental process.