Rae J L, Mathias R T, Cooper K, Baldo G
Department of Physiology, Mayo Foundation, Rochester, MN 55905.
Exp Eye Res. 1992 Jul;55(1):135-44. doi: 10.1016/0014-4835(92)90101-w.
In patch clamp studies of apical membrane from frog lens epithelium, the most frequently observed channel is 'stretch-activated', highly selective for cations over anions but showing little selectivity for Na+ vs. K+. In normal physiological saline, the open channel conductance is 25-30 pS and quite linear over +/- 100 mV. In the absence of extracellular divalent ions, the open channel conductance for inward current flow increases to about 50 pS at the normal lens resting voltage of -75 mV, whereas the conductance for outward current flow is unaffected. In the intact lens, removal of extracellular divalents causes the input conductance approximately to double and the intracellular voltage to depolarize from -74 to -58 mV. A variety of divalent ions block this change in whole lens conductance and voltage in the same order in which they block the 'stretch channels'. Single voltage-clamped epithelial cells also increase their conductance when Ca2+ is removed from their bathing medium. There are, therefore, some striking parallels between the open channel properties of the 'stretch-activated' cation channel and the response of the whole lens or single lens cells to removal of extracellular Ca2+. There are also inconsistencies. This channel is apparently not open in the normal resting lens so removal of extracellular Ca2+ must cause it to open if it is indeed responsible for the increase in lens conductance. However, we have not been able to demonstrate convincingly an increase in open probability at the single-channel level when external divalents are removed.
