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Yoshida, Kosugi
Differences in the electrophysiological response to I- and the inhibitory anions SCN- and ClO-4, studied in FRTL-5 cells.Yoshida A, Sasaki N, Mori A, Taniguchi S, Ueta Y, Hattori K, Tanaka Y, Igawa O, Tsuboi M, Sugawa H, Sato R, Hisatome I, Shigemasa C, Grollman EF, Kosugi S. Biochim Biophys Acta. 1998 Nov 11;1414(1-2):231-7. [abstract only]
"The electrophysiological properties of the Na+/I- symporter (NIS) were examined in a cloned rat thyroid cell line (FRTL-5) using the whole-cell patch-clamp technique. When the holding potential was between -40 mV and -80 mV, 1 mM NaI and NaSCN induced an immediate inward current which was greater with SCN- than with I-. The reversal potential for I- and SCN- induced membrane currents was +50 mV. This is close to the value of +55 mV calculated by the Nernst equation for Na+. These results are consistent with I- and SCN- translocation via the NIS that is energized by the electrochemical gradient of Na+ and coupled to the transport of two or more Na+. There was no change in the membrane current recording with ClO-4 indicating that ClO-4 was either not transported into the cell, or the translocation was electroneutral. ClO-4 addition, however, did reverse the inward currents induced by I- or SCN-. These effects of I-, SCN- and ClO-4 on membrane currents reflect endogenous NIS activity since the responses duplicated those seen in CHO cells transfected with NIS. There were additional currents elicited by SCN- in FRTL-5 cells under certain conditions. For example at holding potentials of 0 and +30 mV, 1 mM SCN- produced an increasingly greater outward current. This outward current was transient. In addition, when SCN- was washed off the cells a transient inward current was detected. Unlike SCN-, 1-10 mM I- had no observable effect on the membrane current at holding potentials of 0 and +30 mV. The results indicate FRTL-5 cells may have a specific SCN- translocation system in addition to the SCN- translocation by the I- porter. Differences demonstrated in current response may explain some of the complicated influx and efflux properties of I-, SCN- and ClO-4 in thyroid cells."
Different electrophysiological character of I-, ClO4-, and SCN- in the transport by Na+/I- symporter.Yoshida A, Sasaki N, Mori A, Taniguchi S, Mitani Y, Ueta Y, Hattori K, Sato R, Hisatome I, Mori T, Shigemasa C, Kosugi S. Biochem Biophys Res Commun. 1997 Feb 24;231(3):731-4. [abstract only]
"The electrophysiological
characteristics of the Na+/I- symporter were examined using the
Chinese hamster ovary (CHO) cell line, which was transfected with the
rat Na+/I- symporter gene and stably expressed the Na+/I- symporter.
In this cell line, iodide uptake was dependent on Na+, and kinetic
studies revealed that the K(m) for iodide was 35 microM, similar to
that of FRTL-5 cells. The maximal velocity at the cell protein level
was 6- to 10-fold higher than in FRTL-5 cells. ClO-4 and SCN-
dose-dependently inhibited iodide uptake in a competitive manner.
Electrophysiological characteristics were examined using the
whole-cell patch-clamp technique. The holding current at-40 mV rapidly
shifted inwardly when the cells were perfused with 1 mEq I- or SCN-.
The inward current induced by 1 mEq I- did not increase when bathing
solution was replaced with a Tyrode solution with 10 mEq I-,
indicating that 1 mEq I- was a saturating amount. The inward current
induced by 1 mEq I- increased 1.5-fold by changing the bathing
solution to a Tyrode solution containing 1 mEq I- and 1 mEq SCN-. The
inward current induced by 0.5 mEq SCN- decreased when the bathing
solution was changed to a Tyrode solution containing 0.5 mEq SCN- and
10 mEq I-. These findings indicated that the I- ion and the SCN- ion
were carried by the NA+/ I- symporter with at least two Na+ ions. The
current induced by the transport of SCN- was larger than that induced
by the transport of I-, possibly because the number of Na+ ions that
was carried with one SCN- ion was larger than the number of Na+ ions
carried with one I- ion. Surprisingly, the perfusion of ClO-4 did not
induce an inward current, indicating that ClO-4 bound to the Na+/I-
symporter, but was not carried by it, or that one ClO-4 ion was
carried with one Na+ ion."
Establishment and characterization of a Chinese hamster ovary cell line, CHO-4J, stably expressing a number of Na+/I- symporters.Kosugi S, Sasaki N, Hai N, Sugawa H, Aoki N, Shigemasa C, Mori T, Yoshida A. Biochem Biophys Res Commun. 1996 Oct 3;227(1):94-101. [abstract only]
"The cDNA of the Na+/I- symporter playing a key role in thyroid iodide transport was cloned very recently. To characterize its function, we transfected the Na+/I- symporter gene into Chinese hamster ovary (CHO) cells and established a cell line stably expressing a number of rat Na+/I- symporters, named CHO-4J. Iodide uptake was dependent on [Na+] and reached a plateau within 30 min. Kinetic studies revealed that the K(m) for iodide was 35 microM, similar to that of FRTL-5 thyroid cells. The maximal velocity (Vmax) at cell protein level was 6-10-fold higher than in FRTL-5 cells and that at single cell level was approximately 1000-fold higher. CIO4- and SCN- dose-dependently inhibited iodide uptake in a competitive manner. The Ki was 1.5 and 16 microM, respectively. Iodide efflux from CHO-4J cells was apparently slower (t1/2 = 15 min) than FRTL-5 cells (t/2 = 2 min). Electrophysiological characteristics were examined using the whole cell patch clamp technique. Rapid inward current was observed when CHO-4J cells were perfused with 50-1000 microM Nal, suggesting a transport stoichiometry of at least 2 Na+ per I-. The current-voltage relation revealed that this current was membrane potential-dependent. The reversal potential was very close to that of Na+ in agreement with dependency on the Na+ electrochemical gradient. CHO-4J cells with a slow iodide efflux, expressing a number of Na+/I-symporters whose characteristics are identical to those of FRTL-5 cells will function as a new tool for sensitive of iodide uptake."
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