ABSTRACT. A correlation between gland stiffness and electrical cell coupling in the salivary gland of Chironomus plumosus was studied by electrophysiological and mechanical measurements. Local anaesthetics, such as alcohols, procaine and chlorpromazine increased gland stiffness. On the other hand, agents influencing cell membrane components, such as glycoletherdiaminetetraacetic acid (EGTA), lipase , trypsin, butylic acid and tetraethylammonium (TEA) decreased gland stiffness. These agents all produced intercellular uncoupling at high concentrations. Alkaline and low medium temperature led to increased gland stiffness and junctional uncoupling. Acid and high medium temperature induced decreased gland stiffness and junctional uncoupling. It was found that gland stiffness had an optimum range (11-27 dyne/cm) for maintenance of cell coupling.Cell communication plays an important role in the regulation of growth and division (7, 18). Loewenstein has postulated (16, 17) that Ca2+ takes part in this cell communication process. However, the role of Ca2+ and ATP in maintaining the structural rigidity of the cell membrane is also well known (1, 4, 5, 22). Intracellular ATP affects cell communication (26). We observed that impalement of gland cells on microelectrodes was either easier or harder depending on the kinds of uncoupling agents applied to the cells. Thus, we suspected that the mechanical properties of the surface of the gland may have been altered after treatment with these agents.We here present a correlation between the mechanical properties of the gland and electrical cell coupling. This was studied by mechanical and electrophysiological methods using the following drugs : local anaesthetics ; TEA and fatty acid as agents influencing the membrane permeability and/or the active transport of Na+, K+ and Ca2+; EGTA, lipase and trypsin as agents influencing the structural components of the cell membrane. The effects of pH and temperature were also examined.A preliminary report has appeared elsewhere (29).
METHODSPreparation. Salivary gland cells of the third and fourth instar larvae of Chironomus plumo-161