TY - JOUR
T1 - Patch-clamp study on ion channels in the tonoplast of nitellopsis obtusa
AU - Katsuhara, Maki
AU - Mimura, Tetsuro
AU - Tazawa, Masashi
N1 - Funding Information:
We are grateful to Dr. M. Kikuyama of Univ. the Air, for his kind advice and many suggestions about the microinjection technique. This work was supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Science and Culture, and by a Grant for Bio-media Program (BMP91III-1-2-C) from the Ministry of Agriculture, Forestry and Fisheries of Japan.
PY - 1991/3
Y1 - 1991/3
N2 - Cytoplasmic drops covered with the tonoplast were prepared from internodal cells of Nitellopsis grown in fresh water. Applying the patch-clamp technique and the microinjection technique to such drops, we characterized the ion channels in the tonoplast. Both in cell-free patches and in the cytoplasmic-drop-attached patches, the tonoplast K+ channel was identified. The permeability ratio between Na+ and K+ was calculated to be 0.2. This channel would provide a molecular basis for the Na+/K+ exchange at the tonoplast. In cell-free patches, the K+channel was not activated by Ca2+. However, in the case of attached patches, microinjection of Ca2+ into a drop activated the K+ channel with a lag of a few seconds, suggesting that some cytoplasmic factor(s) may mediate the activation of the K+ channel by Ca2+. The conductance of this channel was not changed by cytoplasmic Ca2+, but the probability of opening increased markedly. In addition to the K+ channel, a second type of channel was also identified in cell-free patches. This channel may be the Cl- channel.
AB - Cytoplasmic drops covered with the tonoplast were prepared from internodal cells of Nitellopsis grown in fresh water. Applying the patch-clamp technique and the microinjection technique to such drops, we characterized the ion channels in the tonoplast. Both in cell-free patches and in the cytoplasmic-drop-attached patches, the tonoplast K+ channel was identified. The permeability ratio between Na+ and K+ was calculated to be 0.2. This channel would provide a molecular basis for the Na+/K+ exchange at the tonoplast. In cell-free patches, the K+channel was not activated by Ca2+. However, in the case of attached patches, microinjection of Ca2+ into a drop activated the K+ channel with a lag of a few seconds, suggesting that some cytoplasmic factor(s) may mediate the activation of the K+ channel by Ca2+. The conductance of this channel was not changed by cytoplasmic Ca2+, but the probability of opening increased markedly. In addition to the K+ channel, a second type of channel was also identified in cell-free patches. This channel may be the Cl- channel.
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U2 - 10.1093/oxfordjournals.pcp.a078062
DO - 10.1093/oxfordjournals.pcp.a078062
M3 - Article
AN - SCOPUS:0345713570
VL - 32
SP - 179
EP - 184
JO - Plant and Cell Physiology
JF - Plant and Cell Physiology
SN - 0032-0781
IS - 2
ER -