• Media type: E-Article
  • Title: Synergistic Activation of ENaC by Three Membrane-bound Channel-activating Serine Proteases (mCAP1, mCAP2, and mCAP3) and Serum- and Glucocorticoid-regulated Kinase (Sgk1) inXenopusOocytes
  • Contributor: Vuagniaux, Grégoire; Vallet, Véronique; Jaeger, Nicole Fowler; Hummler, Edith; Rossier, Bernard C.
  • imprint: Rockefeller University Press, 2002
  • Published in: The Journal of General Physiology
  • Language: English
  • DOI: 10.1085/jgp.20028598
  • ISSN: 1540-7748; 0022-1295
  • Keywords: Physiology
  • Origination:
  • Footnote:
  • Description: <jats:p>Sodium balance is maintained by the precise regulation of the activity of the epithelial sodium channel (ENaC) in the kidney. We have recently reported an extracellular activation of ENaC-mediated sodium transport (INa) by a GPI-anchored serine protease (mouse channel–activating protein, mCAP1) that was isolated from a cortical collecting duct cell line derived from mouse kidney. In the present study, we have identified two additional membrane-bound serine proteases (mCAP2 and mCAP3) that are expressed in the same cell line. We show that each of these proteases is able to increase INa 6–10-fold in the Xenopus oocyte expression system. INa and the number (N) of channels expressed at the cell surface (measured by binding of a FLAG monoclonal I125-radioiodinated antibody) were measured in the same oocyte. Using this assay, we show that mCAP1 increases INa 10-fold (P &amp;lt; 0.001) but N remained unchanged (P = 0.9), indicating that mCAP1 regulates ENaC activity by increasing its average open probability of the whole cell (wcPo). The serum- and glucocorticoid-regulated kinase (Sgk1) involved in the aldosterone-dependent signaling cascade enhances INa by 2.5-fold (P &amp;lt; 0.001) and N by 1.6-fold (P &amp;lt; 0.001), indicating a dual effect on N and wcPo. Compared with Sgk1 alone, coexpression of Sgk1 with mCAP1 leads to a ninefold increase in INa (P &amp;lt; 0.001) and 1.3-fold in N (P &amp;lt; 0.02). Similar results were observed for mCAP2 and mCAP3. The synergism between CAPs and Sgk1 on INa was always more than additive, indicating a true potentiation. The synergistic effect of the two activation pathways allows a large dynamic range for ENaC-mediated sodium regulation crucial for a tight control of sodium homeostasis.</jats:p>
  • Access State: Open Access