NEUROPEPTIDE STIMULATION OF CALCIUM FLUX IN HUMAN LUNG-CANCER CELLS - DELINEATION OF ALTERNATIVE PATHWAYS

被引:71
作者
BUNN, PA
DIENHART, DG
CHAN, D
PUCK, TT
TAGAWA, M
JEWETT, PB
BRAUNSCHWEIGER, E
机构
[1] UNIV COLORADO,HLTH SCI CTR,DIV MED ONCOL,DENVER,CO 80262
[2] UNIV COLORADO,HLTH SCI CTR,DEPT CHEM,DENVER,CO 80262
[3] ELEANOR ROOSEVELT INST CANC RES,DENVER,CO 80206
关键词
calcium ion dynamics; cellular differentiation; cyclic AMP; growth agonists;
D O I
10.1073/pnas.87.6.2162
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Calcium ion flux following the administration of a series of neuropeptides, N6,O2'-dibutyryladenosine 3',5'-cyclic monophosphate, and serum was monitored by flow cytometry in selected lung and breast cancer cell lines and Chinese hamster ovary cell line CHO-K1. Calcium ion flux was monitored in individual cells by flow cytometry using the indicator indo-1 AM. Five groups of neuropeptides produced calcium flux changes in lung cancer cell lines and CHO-K1 cells but not in breast cancer cells. The peak increase in free calcium was reached within 10 sec of peptide administration and declined to resting levels in 70-120 sec. When two or more members of the same group were administered simultaneously, calcium flux changes were identical to that produced by each single peptide. When two or more members of different groups were administered simultaneously, an increased calcium release occurred. When identical peptides or peptides from the same group were administered sequentially after the return of calcium concentrations to resting values, no calcium flux resulted from the second peptide. When peptides from different active groups were administered sequentially, a new calcium flux occurred after each peptide. These data are interpreted to mean that members of each active group of peptides trigger a different calcium flux pathway. Thus, many such pathways and different metabolic states exist within the cell. Elucidation of calcium flux pathways in normal and cancer cells may lead to greater understanding of the nature of the malignant defect.
引用
收藏
页码:2162 / 2166
页数:5
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