Metalloporphyrin chloride ionophores: Induction of increased anion permeability in lung epithelial cells

被引:15
作者
ElEtri, M
Cuppoletti, J
机构
[1] UNIV CINCINNATI, COLL MED, DEPT CELLULAR & MOLEC PHYSIOL, CINCINNATI, OH 45267 USA
[2] UNIV CINCINNATI, COLL MED, DEPT INTERNAL MED, CINCINNATI, OH 45267 USA
关键词
cystic fibrosis; mouse lung epithelial cells; human lung epithelial cells; ionophores; ion transport; chloride channels; replacement therapy; chloride; short-circuit current; porphin manganese(III) chloride; cystic fibrosis transmembrane regulator; 5,10,15,20-tetraphenyl-21H,23H-porphin manganese(III) chloride;
D O I
10.1152/ajplung.1996.270.3.L386
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Tetraphenyl-21H,23H-porphine manganese(III) chloride [TPPMn(III)] is a positively charged lipophilic anion carrier that is widely used as a Cl- sensor. TPPMn(III) increased anion permeability of cultured mouse lung epithelial (MLE) cells as measured by short-circuit current (I-SC) to a level similar to that induced by forskolin analogues. Anion permeability was also studied in cultured human lung epithelial (A549) cells by measurement of the rates of change of fluorescence of the anion sensitive fluorescent dye, 6-methoxy-N-(3-sulfopropyl)quinolinium (SPQ). In these studies, cells were incubated with SPQ in SO42- medium, washed free of extracellular SPQ, and then perfused with medium containing anions that are known to quench SPQ fluorescence. The effect of TPPMn(III) on anion transport was then determined either microscopically in single cell studies or using cell monolayers mounted in a front face fluorimeter. TPPMn(III) in the range from 1 to 100 mu g/ml induced a dose-dependent increase in Br- transport. The half-maximal quenching effect was estimated to be similar to 5 mu g/ml. TPPMn(III) increased the rates of fluorescence quench of anions by up to fourfold. TPPMn(III) was without effect on [Ca2+](i) level in A549 cells as measured with fura 2-AM. This indicates that TPPMn(III) effects were not mediated through effects on Ca2+-activated Cl- channels, or by compromise of energy metabolism or membrane integrity of the cells. This study suggests that TPPMn(III) and, by extension, other lipophilic Mn(III) or Co(III) derivatives wherein the selectivity or lipophilicity is altered, could increase the anion permeability of biological membranes, and suggests a new approach for treatment of diseases such as cystic fibrosis, where transport of Cl- is defective.
引用
收藏
页码:L386 / L392
页数:7
相关论文
共 25 条
[1]  
ALVAREZLEEFMANS FJ, 1990, CHLORIDE CHANNELS AND CARRIERS IN NERVE, MUSCLE, AND GLIAL CELLS, P3
[2]   ANION SELECTIVITY OF METALLOPORPHYRINS IN MEMBRANES [J].
AMMANN, D ;
HUSER, M ;
KRAUTLER, B ;
RUSTERHOLZ, B ;
SCHULTHESS, P ;
LINDEMANN, B ;
HALDER, E ;
SIMON, W .
HELVETICA CHIMICA ACTA, 1986, 69 (04) :849-854
[3]   GENERATION OF CAMP-ACTIVATED CHLORIDE CURRENTS BY EXPRESSION OF CFTR [J].
ANDERSON, MP ;
RICH, DP ;
GREGORY, RJ ;
SMITH, AE ;
WELSH, MJ .
SCIENCE, 1991, 251 (4994) :679-682
[4]   RELATIONSHIP OF A NON-CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR-MEDIATED CHLORIDE CONDUCTANCE TO ORGAN-LEVEL DISEASE IN CFTR(-/-) MICE [J].
CLARKE, LL ;
GRUBB, BR ;
YANKASKAS, JR ;
COTTON, CU ;
MCKENZIE, A ;
BOUCHER, RC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (02) :479-483
[5]  
CUPPOLETTI J, 1993, Patent No. 5208649
[6]   A CLUSTER OF CYSTIC-FIBROSIS MUTATIONS IN THE 1ST NUCLEOTIDE-BINDING FOLD OF THE CYSTIC-FIBROSIS CONDUCTANCE REGULATOR PROTEIN [J].
CUTTING, GR ;
KASCH, LM ;
ROSENSTEIN, BJ ;
ZIELENSKI, J ;
TSUI, LC ;
ANTONARAKIS, SE ;
KAZAZIAN, HH .
NATURE, 1990, 346 (6282) :366-369
[7]   CHLORIDE CONDUCTANCES OF SALT-SECRETING EPITHELIAL-CELLS [J].
FRIZZELL, RA ;
MORRIS, AP .
CHLORIDE CHANNELS, 1994, 42 :173-214
[8]   SUBSTITUTED METALLOPORPHYRIN DERIVATIVES AS ANION CARRIER FOR PVC MEMBRANE ELECTRODES [J].
GAO, D ;
GU, J ;
YU, RQ ;
ZHENG, GD .
ANALYTICA CHIMICA ACTA, 1995, 302 (2-3) :263-268
[9]  
GRYNKIEWICZ G, 1985, J BIOL CHEM, V260, P3440
[10]  
HARTZELL HC, 1992, MOL PHARMACOL, V41, P880