The 1.3 isoform of Na -Ca2 exchanger expressed in guinea pig tracheal smooth muscle is less sensitive to KB-R7943
Article
-
- Overview
-
- Research
-
- Identity
-
- Additional Document Info
-
- View All
-
Overview
abstract
-
The sodium-calcium exchanger (NCX) plays a major role in the regulation of cytosolic Ca2 in muscle cells. In this work, we performed force experiments to explore the role of NCX during contraction and relaxation of Cch-stimulated guinea pig tracheal smooth muscle strips. This tissue showed low sensitivity to NCX inhibitor KB-R7943 (IC50, 57±2 μM), although a complete relaxation was obtained by NCX inhibition at 100 μM. Interestingly, relaxation after washing the agonist was prolonged in the absence of external Na , whereas washing without Na and in the presence of KB-R7943 resembled control conditions with physiological solution. Altogether, this suggests the reversal of NCX to a Ca2 influx mode by the manipulation on the Na gradient, which can be inhibited by KB-R7943. In order to understand the low sensitivity to KB-R7943, we studied the molecular aspects of the NCX expressed in this tissue and found that the isoform of NCX expressed is 1.3, similar to that described in human tracheal smooth muscle. Sequencing revealed that amino acid 19 in exon B is phenylalanine, whereas in its human counterpart is leucine, and that the first amino acid after exon D is aspartate instead of glutamate in humans. Results herein presented are discussed in term of their possible functional implications in the exchanger activity and thus in airway physiology. © University of Navarra 2010.
-
The sodium-calcium exchanger (NCX) plays a major role in the regulation of cytosolic Ca2%2b in muscle cells. In this work, we performed force experiments to explore the role of NCX during contraction and relaxation of Cch-stimulated guinea pig tracheal smooth muscle strips. This tissue showed low sensitivity to NCX inhibitor KB-R7943 (IC50, 57±2 μM), although a complete relaxation was obtained by NCX inhibition at 100 μM. Interestingly, relaxation after washing the agonist was prolonged in the absence of external Na%2b, whereas washing without Na%2b and in the presence of KB-R7943 resembled control conditions with physiological solution. Altogether, this suggests the reversal of NCX to a Ca2%2b influx mode by the manipulation on the Na%2b gradient, which can be inhibited by KB-R7943. In order to understand the low sensitivity to KB-R7943, we studied the molecular aspects of the NCX expressed in this tissue and found that the isoform of NCX expressed is 1.3, similar to that described in human tracheal smooth muscle. Sequencing revealed that amino acid 19 in exon B is phenylalanine, whereas in its human counterpart is leucine, and that the first amino acid after exon D is aspartate instead of glutamate in humans. Results herein presented are discussed in term of their possible functional implications in the exchanger activity and thus in airway physiology. © University of Navarra 2010.
publication date
published in
Research
keywords
-
Airway smooth muscle; Guinea pig; Isoform; KB-R7943; NCX 2 [2 [4 (4 nitrobenzyloxy)phenyl]ethyl]isothiourea methanesulfonate; aspartic acid; glutamic acid; leucine; nifedipine; phenylalanine; sodium calcium exchange protein; amino acid sequence; animal tissue; article; calcium transport; controlled study; exon; guinea pig; molecular biology; muscle contraction; muscle relaxation; nonhuman; nucleotide sequence; reverse transcription polymerase chain reaction; smooth muscle; trachea; Amino Acid Sequence; Animals; Base Sequence; Calcium; Guinea Pigs; Male; Molecular Sequence Data; Muscle Contraction; Muscle Relaxation; Myocytes, Smooth Muscle; Protein Isoforms; Sodium-Calcium Exchanger; Thiourea; Trachea; Cavia
Identity
Digital Object Identifier (DOI)
PubMed ID
Additional Document Info
start page
end page
volume
issue