Abstract
We have investigated the role of an aprotinin-sensitive protease in regulating Ca(2+)-ATPase activity and Ca2+ uptake (ATP-dependent and Na(+)-dependent) in microsomes of bovine pulmonary vascular smooth muscle during treatment with the O2(-.)-generating system hypoxanthine plus xanthine oxidase. Treatment of the smooth muscle microsomes with the O2(-.)-generating system produced a protease in a gelatin-containing zymogram with an apparent molecular mass of 16 kDa. This 16 kDa proteolytic protein was found to be inhibited by superoxide dismutase (SOD) and aprotinin but not by PMSF. Using polyclonal antiserum to aprotinin, we found that it is an ambient antiprotease of the smooth muscle microsomes. Treatment of the microsomes with the O2(-.)-generating system stimulated protease activity tested with a synthetic substrate N-benzoyl-DL-arginine p-nitroanilide and also enhanced Ca(2+)-ATPase activity. It also stimulated ATP-dependent Ca2+ uptake. In contrast, Na(+)-dependent Ca2+ uptake was found to be inhibited by the O2(-.)-generating system. Pretreatment of the microsomes with SOD and aprotinin preserved the increase in protease activity, Ca(2+)-ATPase activity and ATP-dependent Ca2+ uptake. In addition, O2(-.)-caused inhibition of the Na(+)-dependent Ca2+ uptake which was reversed by SOD and aprotinin. Pretreatment with PMSF did not cause any discernible alteration in the protease activity, Ca(2+)-ATPase activity. ATP-dependent Ca2+ uptake and Na(+)-dependent Ca2+ uptake in the microsomes caused by the O2(-.)-generating system. These results suggest that an aprotinin-sensitive protease plays a pivotal role in regulating Ca(2+)-ATPase and Ca(2+)-uptake activities in microsomes of pulmonary vascular smooth muscle under oxidant O2(-.)-triggered conditions.
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- Au K. S. Activation of erythrocyte membrane Ca2+-ATPase by calpain. Biochim Biophys Acta. 1987 Dec 11;905(2):273–278. doi: 10.1016/0005-2736(87)90455-x. [DOI] [PubMed] [Google Scholar]
- Baumhüter S., Richter C. The hydroperoxide-induced release of mitochondrial calcium occurs via a distinct pathway and leaves mitochondria intact. FEBS Lett. 1982 Nov 8;148(2):271–275. doi: 10.1016/0014-5793(82)80823-5. [DOI] [PubMed] [Google Scholar]
- Bennett A. M., Williams G. M. Alteration of rat liver endoplasmic reticulum Ca(2+)-ATPase thiol integrity by ciprofibrate, a peroxisome proliferator. Biochem Pharmacol. 1993 May 25;45(10):2093–2098. doi: 10.1016/0006-2952(93)90021-n. [DOI] [PubMed] [Google Scholar]
- Bennett A. M., Williams G. M. Alteration of rat liver endoplasmic reticulum Ca(2+)-ATPase thiol integrity by ciprofibrate, a peroxisome proliferator. Biochem Pharmacol. 1993 May 25;45(10):2093–2098. doi: 10.1016/0006-2952(93)90021-n. [DOI] [PubMed] [Google Scholar]
- Berridge M. J. Inositol trisphosphate and calcium signalling. Nature. 1993 Jan 28;361(6410):315–325. doi: 10.1038/361315a0. [DOI] [PubMed] [Google Scholar]
- Bharadwaj D., Roy M. S., Bose D., Hati R. N. A new blood-coagulating protease in mitochondrial membranes of rat submaxillary glands. Purification and characterization of protease and its blood-coagulating activity. J Biol Chem. 1994 Jun 10;269(23):16229–16235. [PubMed] [Google Scholar]
- Billings P. C., Habres J. M., Liao D. C., Tuttle S. W. Human fibroblasts contain a proteolytic activity which is inhibited by the Bowman-Birk protease inhibitor. Cancer Res. 1991 Oct 15;51(20):5539–5543. [PubMed] [Google Scholar]
- Bond J. S., Butler P. E. Intracellular proteases. Annu Rev Biochem. 1987;56:333–364. doi: 10.1146/annurev.bi.56.070187.002001. [DOI] [PubMed] [Google Scholar]
- Carafoli E. Biogenesis: plasma membrane calcium ATPase: 15 years of work on the purified enzyme. FASEB J. 1994 Oct;8(13):993–1002. [PubMed] [Google Scholar]
- Chakraborti S., Chakraborti T. Down-regulation of protein kinase C attenuates the oxidant hydrogen peroxide-mediated activation of phospholipase A2 in pulmonary vascular smooth muscle cells. Cell Signal. 1995 Jan;7(1):75–83. doi: 10.1016/0898-6568(94)00061-f. [DOI] [PubMed] [Google Scholar]
- Chakraborti S., Gurtner G. H., Michael J. R. Oxidant-mediated activation of phospholipase A2 in pulmonary endothelium. Am J Physiol. 1989 Dec;257(6 Pt 1):L430–L437. doi: 10.1152/ajplung.1989.257.6.L430. [DOI] [PubMed] [Google Scholar]
- Chakraborti S., Michael J. R., Gurtner G. H., Ghosh S. S., Dutta G., Merker A. Role of a membrane-associated serine esterase in the oxidant activation of phospholipase A2 by t-butyl hydroperoxide. Biochem J. 1993 Jun 1;292(Pt 2):585–589. doi: 10.1042/bj2920585. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chakraborti S., Michael J. R., Sanyal T. Defining the role of protein kinase c in calcium-ionophore-(A23187)-mediated activation of phospholipase A2 in pulmonary endothelium. Eur J Biochem. 1992 Jun 15;206(3):965–972. doi: 10.1111/j.1432-1033.1992.tb17007.x. [DOI] [PubMed] [Google Scholar]
- Clark M. L., Lanz H. C., Senior J. R. Enzymatic distinction of rat intestinal cell brush border and endoplasmic reticular membranes. Biochim Biophys Acta. 1969 Jun 3;183(1):233–235. doi: 10.1016/0005-2736(69)90147-3. [DOI] [PubMed] [Google Scholar]
- Davis B. A., Edes I., Gupta R. C., Young E. F., Kim H. W., Steenaart N. A., Szymanska G., Kranias E. G. The role of phospholamban in the regulation of calcium transport by cardiac sarcoplasmic reticulum. Mol Cell Biochem. 1990 Dec 20;99(2):83–88. doi: 10.1007/BF00230337. [DOI] [PubMed] [Google Scholar]
- Dixon I. M., Kaneko M., Hata T., Panagia V., Dhalla N. S. Alterations in cardiac membrane Ca2+ transport during oxidative stress. Mol Cell Biochem. 1990 Dec 20;99(2):125–133. doi: 10.1007/BF00230342. [DOI] [PubMed] [Google Scholar]
- Eggermont J. A., Vrolix M., Raeymaekers L., Wuytack F., Casteels R. Ca2+-transport ATPases of vascular smooth muscle. Circ Res. 1988 Feb;62(2):266–278. doi: 10.1161/01.res.62.2.266. [DOI] [PubMed] [Google Scholar]
- Farrukh I. S., Michael J. R., Summer W. R., Adkinson N. F., Jr, Gurtner G. H. Thromboxane-induced pulmonary vasoconstriction: involvement of calcium. J Appl Physiol (1985) 1985 Jan;58(1):34–44. doi: 10.1152/jappl.1985.58.1.34. [DOI] [PubMed] [Google Scholar]
- Freeman B. A., Crapo J. D. Biology of disease: free radicals and tissue injury. Lab Invest. 1982 Nov;47(5):412–426. [PubMed] [Google Scholar]
- Ghosh J., Ray M., Sarkar S., Bhaduri A. A high affinity Ca2(+)-ATPase on the surface membrane of Leishmania donovani promastigote. J Biol Chem. 1990 Jul 5;265(19):11345–11351. [PubMed] [Google Scholar]
- Ghosh T. K., Mullaney J. M., Tarazi F. I., Gill D. L. GTP-activated communication between distinct inositol 1,4,5-trisphosphate-sensitive and -insensitive calcium pools. Nature. 1989 Jul 20;340(6230):236–239. doi: 10.1038/340236a0. [DOI] [PubMed] [Google Scholar]
- Grover A. K. Ca-pumps in smooth muscle: one in plasma membrane and another in endoplasmic reticulum. Cell Calcium. 1985 Jun;6(3):227–236. doi: 10.1016/0143-4160(85)90008-9. [DOI] [PubMed] [Google Scholar]
- Holzer H., Heinrich P. C. Control of proteolysis. Annu Rev Biochem. 1980;49:63–91. doi: 10.1146/annurev.bi.49.070180.000431. [DOI] [PubMed] [Google Scholar]
- Kadoma M., Froehlich J., Reeves J., Sutko J. Kinetics of sodium ion induced calcium ion release in calcium ion loaded cardiac sarcolemmal vesicles: determination of initial velocities by stopped-flow spectrophotometry. Biochemistry. 1982 Apr 13;21(8):1914–1918. doi: 10.1021/bi00537a033. [DOI] [PubMed] [Google Scholar]
- Ketis N. V., Hoover R. L., Karnovsky M. J. Isolation of bovine aortic endothelial cell plasma membranes: identification of membrane-associated cytoskeletal proteins. J Cell Physiol. 1986 Aug;128(2):162–170. doi: 10.1002/jcp.1041280205. [DOI] [PubMed] [Google Scholar]
- Koh E., Morimoto S., Fukuo K., Shiraishi T., Hironaka T., Onishi T., Kumahara Y. Effects of nitrates and calcium channel blockers on Ca2+-ATPase in the microsomal fraction of porcine coronary artery smooth muscle cells. Cell Calcium. 1987 Oct;8(5):397–410. doi: 10.1016/0143-4160(87)90014-5. [DOI] [PubMed] [Google Scholar]
- Kosk-Kosicka D., Inesi G. Cooperative calcium binding and calmodulin regulation in the calcium-dependent adenosine triphosphatase purified from the erythrocyte membrane. FEBS Lett. 1985 Sep 9;189(1):67–71. doi: 10.1016/0014-5793(85)80843-7. [DOI] [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- Lottenberg R., Christensen U., Jackson C. M., Coleman P. L. Assay of coagulation proteases using peptide chromogenic and fluorogenic substrates. Methods Enzymol. 1981;80(Pt 100):341–361. doi: 10.1016/s0076-6879(81)80030-4. [DOI] [PubMed] [Google Scholar]
- Mancini G., Carbonara A. O., Heremans J. F. Immunochemical quantitation of antigens by single radial immunodiffusion. Immunochemistry. 1965 Sep;2(3):235–254. doi: 10.1016/0019-2791(65)90004-2. [DOI] [PubMed] [Google Scholar]
- Mellgren R. L., Mericle M. T., Lane R. D. Proteolysis of the calcium-dependent protease inhibitor by myocardial calcium-dependent protease. Arch Biochem Biophys. 1986 Apr;246(1):233–239. doi: 10.1016/0003-9861(86)90468-6. [DOI] [PubMed] [Google Scholar]
- Murray P. A., Lodato R. F., Michael J. R. Neural antagonists modulate pulmonary vascular pressure-flow plots in conscious dogs. J Appl Physiol (1985) 1986 Jun;60(6):1900–1907. doi: 10.1152/jappl.1986.60.6.1900. [DOI] [PubMed] [Google Scholar]
- Murray P. A., Lodato R. F., Michael J. R. Neural antagonists modulate pulmonary vascular pressure-flow plots in conscious dogs. J Appl Physiol (1985) 1986 Jun;60(6):1900–1907. doi: 10.1152/jappl.1986.60.6.1900. [DOI] [PubMed] [Google Scholar]
- Neyses L., Reinlib L., Carafoli E. Phosphorylation of the Ca2+-pumping ATPase of heart sarcolemma and erythrocyte plasma membrane by the cAMP-dependent protein kinase. J Biol Chem. 1985 Aug 25;260(18):10283–10287. [PubMed] [Google Scholar]
- Pershadsingh H. A., McDonald J. M. A high affinity calcium-stimulated magnesium-dependent adenosine triphosphatase in rat adipocyte plasma membranes. J Biol Chem. 1980 May 10;255(9):4087–4093. [PubMed] [Google Scholar]
- Qu Y., Torchia J., Sen A. K. Protein kinase C mediated activation and phosphorylation of Ca(2+)-pump in cardiac sarcolemma. Can J Physiol Pharmacol. 1992 Sep;70(9):1230–1235. doi: 10.1139/y92-171. [DOI] [PubMed] [Google Scholar]
- Qu Y., Torchia J., Sen A. K. Protein kinase C mediated activation and phosphorylation of Ca(2+)-pump in cardiac sarcolemma. Can J Physiol Pharmacol. 1992 Sep;70(9):1230–1235. doi: 10.1139/y92-171. [DOI] [PubMed] [Google Scholar]
- Raeymaekers L., Wuytack F., Casteels R. Subcellular fractionation of pig stomach smooth muscle. A study of the distribution of the (Ca2+ + Mg2+)-ATPase activity in plasmalemma and endoplasmic reticulum. Biochim Biophys Acta. 1985 May 28;815(3):441–454. doi: 10.1016/0005-2736(85)90372-4. [DOI] [PubMed] [Google Scholar]
- Robinson B. F., Collier J. G., Karim S. M., Somers K. Effect of prostaglandins A 1 , A 2 , B 1 , E 2 and F 2 on forearm arterial bed and superficial hand veins in man. Clin Sci. 1973 Apr;44(4):367–376. doi: 10.1042/cs0440367. [DOI] [PubMed] [Google Scholar]
- Scherer N. M., Deamer D. W. Oxidative stress impairs the function of sarcoplasmic reticulum by oxidation of sulfhydryl groups in the Ca2+-ATPase. Arch Biochem Biophys. 1986 May 1;246(2):589–601. doi: 10.1016/0003-9861(86)90314-0. [DOI] [PubMed] [Google Scholar]
- Seeger W., Wolf H., Graubert E., Moser U., Neuhof H., Roka L. Influence of aprotinin and gabexate mesilate on arachidonic acid release by the Ca-ionophore A 23187 in the lung. Adv Exp Med Biol. 1983;156:553–567. [PubMed] [Google Scholar]
- Tate R. M., Vanbenthuysen K. M., Shasby D. M., McMurtry I. F., Repine J. E. Oxygen-radical-mediated permeability edema and vasoconstriction in isolated perfused rabbit lungs. Am Rev Respir Dis. 1982 Nov;126(5):802–806. doi: 10.1164/arrd.1982.126.5.802. [DOI] [PubMed] [Google Scholar]
- Zurini M., Krebs J., Penniston J. T., Carafoli E. Controlled proteolysis of the purified Ca2+-ATPase of the erythrocyte membrane. A correlation between the structure and the function of the enzyme. J Biol Chem. 1984 Jan 10;259(1):618–627. [PubMed] [Google Scholar]
