Connexin Hemichannel Composition Determines the FGF-1–induced Membrane Permeability and Free [Ca2+]iResponses

Abstract

Cell surface hemichannels (HCs) composed of different connexin (Cx) types are present in diverse cells and their possible role on FGF-1–induced cellular responses remains unknown. Here, we show that FGF-1 transiently (4–14 h, maximal at 7 h) increases the membrane permeability through HCs in HeLa cells expressing Cx43 or Cx45 under physiological extracellular Ca2+/Mg2+concentrations. The effect does not occur in HeLa cells expressing HCs constituted of Cx26 or Cx43 with its C-terminus truncated at aa 257, or in parental nontransfected HeLa cells. The increase in membrane permeability is associated with a rise in HC levels at the cell surface and a proportional increase in HC unitary events. The response requires an early intracellular free Ca2+concentration increase, activation of a p38 MAP kinase-dependent pathway, and a regulatory site of Cx subunit C-terminus. The FGF-1–induced rise in membrane permeability is also associated with a late increase in intracellular free Ca2+concentration, suggesting that responsive HCs allow Ca2+influx. The cell density of Cx26 and Cx43 HeLa transfectants cultured in serum-free medium was differentially affected by FGF-1. Thus, the FGF-1–induced cell permeabilization and derived consequences depend on the Cx composition of HCs.