TY - JOUR
T1 - Ba2+ current oscillations modulated by cyclic AMP and phorbol esters in ras-transformed fibroblasts
AU - Higashida, Haruhiro
AU - Hoshi, Naoto
AU - Noda, Mami
AU - Shahidullah, Mohammad
AU - Hashii, Minako
AU - Nozawa, Yoshinori
N1 - Funding Information:
Acknowledpments, We thank Mary Ann Mooradian for reading the manuscript. This work was supported by grants from the JapaneseM inistry of Education, Science & Culture.
PY - 1992/2/14
Y1 - 1992/2/14
N2 - An oscillatory influx of divalent cations was measured as Ba2+ inward currents (Ba2+ current oscillations) by voltage-clamp recording in v-Ki-ras-transformed NIH 3T3 (DT) fibroblasts after activation with bradykinin or serum. Application of forskolin or dibutyryl cyclic AMP onto DT cells initiated Ba2+ current oscillations. Increasing intracellular cyclic AMP reduced the amplitude but increased the frequency of the Ba2+ current oscillations. Activation of protein kinase C by phorbol esters terminated Ba2+ current oscillations. No inhibition of Ba2+ current oscillations by phorbol esters was observed in down-regulated cells that had been pretreated with phorbol esters for 24 hrs. The results suggest that Ba2+ current oscillations are regulated by intracellular second messengers.
AB - An oscillatory influx of divalent cations was measured as Ba2+ inward currents (Ba2+ current oscillations) by voltage-clamp recording in v-Ki-ras-transformed NIH 3T3 (DT) fibroblasts after activation with bradykinin or serum. Application of forskolin or dibutyryl cyclic AMP onto DT cells initiated Ba2+ current oscillations. Increasing intracellular cyclic AMP reduced the amplitude but increased the frequency of the Ba2+ current oscillations. Activation of protein kinase C by phorbol esters terminated Ba2+ current oscillations. No inhibition of Ba2+ current oscillations by phorbol esters was observed in down-regulated cells that had been pretreated with phorbol esters for 24 hrs. The results suggest that Ba2+ current oscillations are regulated by intracellular second messengers.
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U2 - 10.1016/0006-291X(92)91864-M
DO - 10.1016/0006-291X(92)91864-M
M3 - Article
C2 - 1311569
AN - SCOPUS:0026611397
SN - 0006-291X
VL - 182
SP - 1240
EP - 1245
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 3
ER -