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Am J Physiol Cell Physiol 275: C619-C621, 1998;
0363-6143/98 $5.00
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Vol. 275, Issue 2, C619-C621, August 1998

SPECIAL COMMUNICATION
Using gadolinium to identify stretch-activated channels: technical considerations

Ray A. Caldwell1, Henry F. Clemo1,2, and Clive M. Baumgarten1

Departments of 1 Physiology and 2 Medicine, Medical College of Virginia, Virginia Commonwealth University, Richmond, Virginia 23298

Gadolinium (Gd3+) blocks cation-selective stretch-activated ion channels (SACs) and thereby inhibits a variety of physiological and pathophysiological processes. Gd3+ sensitivity has become a simple and widely used method for detecting the involvement of SACs, and, conversely, Gd3+ insensitivity has been used to infer that processes are not dependent on SACs. The limitations of this approach are not adequately appreciated, however. Avid binding of Gd3+ to anions commonly present in physiological salt solutions and culture media, including phosphate- and bicarbonate-buffered solutions and EGTA in intracellular solutions, often is not taken into account. Failure to detect an effect of Gd3+ in such solutions may reflect the vanishingly low concentrations of free Gd3+ rather than the lack of a role for SACs. Moreover, certain SACs are insensitive to Gd3+, and Gd3+ also blocks other ion channels. Gd3+ remains a useful tool for studying SACs, but appropriate care must be taken in experimental design and interpretation to avoid both false negative and false positive conclusions.

mechanosensitive channels; mechanoelectrical feedback; lanthanides; chelation


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