Literature DB >> 6706926

Stimulation of Na+-Ca2+ exchange in cardiac sarcolemmal vesicles by phospholipase D.

K D Philipson, A Y Nishimoto.   

Abstract

Treatment of canine cardiac sarcolemmal vesicles with phospholipase D resulted in a large stimulation (up to 400%) of Na+-Ca2+ exchange activity. The phospholipase D treatment decreased the apparent Km (Ca2+) for the initial rate of Nai+-dependent Ca2+ uptake from 18.2 +/- 2.6 to 6.3 +/- 0.3 microM. The Vmax increased from 18.0 +/- 3.6 to 31.5 +/- 3.6 nmol of Ca2+/mg of protein/s. The effect was specific for Na+-Ca2+ exchange; other sarcolemmal transport enzymes ((Na+, K+)-ATPase; ATP-dependent Ca2+ transport) are inhibited by incubation with phospholipase D. Phospholipase D had little effect on the passive Ca2+ permeability of the sarcolemmal vesicles. After treatment with 0.4 unit/ml of phospholipase D (20 min, 37 degrees C), the sarcolemmal content of phosphatidic acid rose from 0.9 +/- 0.2 to 8.9 +/- 0.4%; simultaneously, Na+-Ca2+ exchange activity increased 327 +/- 87%. It is probable that the elevated phosphatidic acid level is responsible for the enhanced Na+-Ca2+ exchange activity. In a previous study (Philipson, K. D., Frank, J. S., and Nishimoto, A. Y. (1983) J. Biol. Chem. 258, 5905-5910), we hypothesized that negatively charged phospholipids were important in Na+-Ca2+ exchange, and the present results are consistent with this hypothesis. Stimulation of Na+-Ca2+ exchange by phosphatidic acid may be important in explaining the Ca2+ influx which accompanies the phosphatidylinositol turnover response which occurs in a wide variety of tissues.

Entities:  

Mesh:

Substances:

Year:  1984        PMID: 6706926

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  15 in total

Review 1.  Sarcolemmal calcium binding sites in heart: II. Mathematical model for diffusion of calcium released from the sarcoplasmic reticulum into the diadic region.

Authors:  A Peskoff; J A Post; G A Langer
Journal:  J Membr Biol       Date:  1992-07       Impact factor: 1.843

Review 2.  Regulation and functional significance of phospholipase D in myocardium.

Authors:  Y E Eskildsen-Helmond; H A Van Heugten; J M Lamers
Journal:  Mol Cell Biochem       Date:  1996 Apr 12-26       Impact factor: 3.396

3.  Roles of proteins in cation/membrane interactions of isolated rat cardiac sarcolemmal vesicles.

Authors:  K S Leonards
Journal:  Mol Cell Biochem       Date:  1990-06-01       Impact factor: 3.396

4.  Kinetics of myocardial phospholipase D.

Authors:  J Dai; S Y Liu; V Panagia
Journal:  Mol Cell Biochem       Date:  1996 Jul-Aug       Impact factor: 3.396

Review 5.  The receptor-regulated calcium influx in mouse submandibular acinar cells is sodium dependent: a patch-clamp study.

Authors:  D V Gallacher; A P Morris
Journal:  J Physiol       Date:  1987-03       Impact factor: 5.182

6.  Modulation of Na+-Ca2+ exchange in cardiac sarcolemmal vesicles by Ca2+ antagonists.

Authors:  T Hata; N Makino; H Nakanishi; T Yanaga
Journal:  Mol Cell Biochem       Date:  1988-11       Impact factor: 3.396

7.  The mitogenic activities of phosphatidate are acyl-chain-length dependent and calcium independent in C3H/10T1/2 cells.

Authors:  M J Krabak; S W Hui
Journal:  Cell Regul       Date:  1991-01

8.  Mechanism of cardiac Na(+)-Ca2+ exchange current stimulation by MgATP: possible involvement of aminophospholipid translocase.

Authors:  D W Hilgemann; A Collins
Journal:  J Physiol       Date:  1992-08       Impact factor: 5.182

9.  Signal transduction mechanism for the stimulation of the sarcolemmal Na(+)-Ca2+ exchanger by insulin.

Authors:  C Ballard; M Mozaffari; S Schaffer
Journal:  Mol Cell Biochem       Date:  1994-06-15       Impact factor: 3.396

10.  Characterization of choline efflux from the perfused heart at rest and after muscarine receptor activation.

Authors:  R Lindmar; K Löffelholz; J Sandmann
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1986-03       Impact factor: 3.000

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.