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Licensed Unlicensed Requires Authentication Published by De Gruyter May 15, 2015

Biochemical evidence for Ca2+-independent functional activation of hPLSCR1 at low pH

  • Vincent Gerard Francis and Sathyanarayana N. Gummadi EMAIL logo

Abstract

Human phospholipid scramblase 1 (hPLSCR1) is a Ca2+-dependent protein known to scramble phospholipids in the plasma membrane resulting in loss of membrane asymmetry. It has been reported that hPLSCR1 exhibits Ca2+- independent activity at low pH. However, the conformational changes induced at low pH leading to functional activation are not known. Our results showed that recombinant hPLSCR1 was functionally activated at low pH, which is similar to the behavior of natively extracted hPLSCR1. Tryptophan fluorescence measurements showed a decrease in Ca2+-binding affinity at low pH, although not at pH 5.5. Far and near UV-CD revealed that low pH induced structural changes, with a significant increase in the β-sheet content of the protein. At the physiological level, decreased hPLSCR1 expression was observed after a period of exposure to low pH. The effect occurred at the promoter level. The expression levels of hPLSCR1 directly correlated with the sensitivity of HEK293 to apoptosis. Based on these results, we conclude that the mechanisms of Ca2+- and pH-induced functional activation of hPLSCR1 are different and that hPLSCR1 expression regulated by low pH could provide insights into the role of hPLSCR1 in cancer progression.

References

1. Gummadi, S.N and Kumar, S.K. The mysetery of phospholipid flp-flop in biogenic membranes. Cell. Mol. Biol. Lett. 10 (2007) 101-121.Search in Google Scholar

2. Sims, P.J. and Wiedmer, T. Unraveling the mysteries of phospholipid scrambling. Thromb. Haemost. 86 (2001) 266-275.Search in Google Scholar

3. Zhou, Q., Zhao, J., Wiedmer, T. and Sims, P.J. Normal hemostasis but defective hematopoietic response to growth factors in mice deficient in phospholipid scramblase 1. Blood 99 (2002) 4030-4038.Search in Google Scholar

4. Chen, M.H., Ben-Efraim, I., Mitrousis, G., Walker-Kopp, N., Sims, P.J. and Cingolani, G. Phospholipid scramblase 1 contains a nonclassical nuclear localization signal with unique binding site in importin alpha. J. Biol. Chem. 280 (2005) 10599-10606.Search in Google Scholar

5. Zhou, Q., Ben-Efraim, I., Bigcas, J-L., Junqueira, D., Wiedmer, T. and Sims, P.J. Phospholipid scramblase 1 binds to the promoter region of the inositol 1,4,5-triphosphate receptor type 1 gene to enhance its expression. J. Biol. Chem. 280 (2005) 35062-35068.Search in Google Scholar

6. Wyles, J.P., Wu, Z., Mirski, S.E.L. and Cole, S.P.C. Nuclear interactions of topoisomerase II alpha and beta with phospholipid scramblase 1. Nucleic Acids Res. 35 (2007) 4076-4085.Search in Google Scholar

7. Sun, J., Zhao, J., Schwartz, M.A., Wang, J.Y., Wiedmer, T. and Sims, P.J. c-Abl tyrosine kinase binds and phosphorylates phospholipid scramblase 1. J. Biol. Chem. 276 (2001) 28984-28990.Search in Google Scholar

8. Dong, B., Zhou, Q., Zhao, Q., Zhou, A., Harty, R.N. and Bose, S. Phospholipid scramblase 1 potentiates the antiviral activity of interferon. J. Virol. 78 (2004) 8983-8993.Search in Google Scholar

9. Li, Y., Rogulski, K., Zhou, Q., Sims, P.J. and Prochownik, E.V. The negative c-Myc target onzin affects proliferation and apoptosis via its obligate interaction with phospholipid scramblase 1. Mol. Cell. Biol. 26 (2006) 3401-3413.Search in Google Scholar

10. Merregaert, J.,Van-Langen, J., Hansen, U., Ponsaerts, P., El-Ghalbzouri, A., Steenackers, E., Van-Ostade, X. and Sercu, S. Phospholipid scramblase 1 is secreted by a lipid raft-dependent pathway and interacts with the extracellular matrix protein 1 in the dermal epidermal junction zone of human skin. J. Biol. Chem. 285 (2010) 37823-37837.Search in Google Scholar

11. Py, B., Basmaciogullari, S., Bouchet, J., Zarka, M., Moura, I.C., Benhamou, M., Monteiro, R.C., Hocini, H., Madrid, R. and Benichou, S. The phospholipid scramblases 1 and 4 are cellular receptors for the secretory leukocyte protease inhibitor and interact with CD4 at the plasma membrane. PLoS ONE 4 (2009) e5006.10.1371/journal.pone.0005006Search in Google Scholar PubMed PubMed Central

12. Gong, Q., Cheng, M., Chen, H., Liu, X., Si, Y., Yang, Y., Yuan, Y., Jin, C., Yang, W., He, F. and Wang, J. Phospholipid scramblase 1 mediates hepatitis C virus entry into host cells. FEBS Lett. 585 (2011) 2647-2652.Search in Google Scholar

13. Stout, J.G., Bassé, F., Luhm, R.A., Weiss, H.J., Wiedmer, T. and Sims, P.J. Scott syndrome erythrocytes contain a membrane protein capable of mediating Ca2+-dependent transbilayer migration of membrane phospholipids. J. Clin. Invest. 99 (1997) 2232-2238.Search in Google Scholar

14. Suzuki, J., Umeda, M., Sims, P.J. and Nagata, S. Calcium-dependent phospholipid scrambling by TMEM16F. Nature 468 (2010) 834-838.Search in Google Scholar

15. Busa, W.B. and Nuccitelli, R. Metabolic regulation via intracellular pH. Am. J. Physiol. 246 (1984) R409-438.10.1152/ajpregu.1984.246.4.R409Search in Google Scholar PubMed

16. OuYang, Y.B., Mellergård, P., Kristián, T., Kristiánova, V. and Siesjö, B.K. Influence of acid-base changes on the intracellular calcium concentration of neurons in primary culture. Exp. Brain Res. 101 (1994) 265-271.Search in Google Scholar

17. Capuano, P. and Capasso, G. The importance of intracellular pH in the regulation of cell function. G. Ital. Nefrol. 20 (2003) 139-150.Search in Google Scholar

18. Grinstein, S., Swallow, C.J. and Rotstein, O.D. Regulation of cytoplasmic pH in phagocytic cell function and dysfunction. Clin. Biochem. 24 (1991) 241-247.Search in Google Scholar

19. Schelling, J.R. and Abu-Jawdeh, B.G. Regulation of cell survival by Na+/H+ exchanger-1. Am. J. Physiol. Renal Physiol. 295 (2008) F625-632.10.1152/ajprenal.90212.2008Search in Google Scholar PubMed PubMed Central

20. Reshkin, S.J., Cardone, R.A. and Harguindey, S. Na+-H+ exchanger, pH regulation and cancer. Recent Pat. Anticancer Drug Discov. 8 (2013) 85-99.10.2174/1574892811308010085Search in Google Scholar

21. Amith, S.R. and Fliegel, L. Regulation of the Na+/H+ exchanger (NHE1) in breast cancer metastasis. Cancer Res. 73 (2013) 1259-1264.Search in Google Scholar

22. Mellman, I., Fuchs, R. and Helenius, A. Acidification of the endocytic and exocytic pathways. Annu. Rev. Biochem. 55 (1986) 663-700.Search in Google Scholar

23. Glunde, K., Guggino, S.E., Solaiyappan, M., Pathak, A.P., Ichikawa, Y. and Bhujwalla, Z.M. Extracellular acidification alters lysosomal trafficking in human breast cancer cells. Neoplasia 5 (2003) 533-545.Search in Google Scholar

24. Tannock, I.F. and Rotin, D. Acid pH in tumors and its potential for therapeutic exploitation. Cancer Res. 49 (1989) 4373-4384.Search in Google Scholar

25. Lardner, A. The effects of extracellular pH on immune function. J. Leukoc. Biol. 69 (2001) 522-530.Search in Google Scholar

26. Ward, T.T. and Steigbigel, R.T. Acidosis of synovial fluid correlates with synovial fluid leukocytosis. Am. J. Med. 64 (1978) 933-936.Search in Google Scholar

27. Estrella, V., Chen, T., Lloyd, M., Wojtkowiak, J., Cornnell, H.H., Ibrahim- Hashim, A., Bailey, K., Balagurunathan, Y., Rothberg, J.M., Sloane, B.F., Johnson, F., Gatenby, R.A. and Gillies, R.J. Acidity generated by the tumor microenvironment drives local invasion. Cancer Res. 73 (2013) 1524-1535.Search in Google Scholar

28. Xu, L., Fukumura, D. and Jain, R.K. Acidic extracellular pH induces vascular endothelial growth factor (VEGF) in human glioblastoma cells via ERK1/2 MAPK signaling pathway: mechanism of low pH-induced VEGF. J. Biol. Chem. 277 (2002) 11368-11374.Search in Google Scholar

29. Chiche, J., Ilc, K., Laferrière, J., Trottier, E., Dayan, F., Mazure, N.M., Brahmini-Horn, M.C. and Pouyssequr, J. Hypoxia-inducible carbonic anhydrase IX and XII promote tumor cell growth by counteracting acidosis through the regulation of the intracellular pH. Cancer Res. 69 (2009) 358-368.Search in Google Scholar

30. Mishra, A., Shiozawa, Y., Pienta, K.J. and Taichman, R.S. Homing of cancer cells to the bone. Cancer Microenviron. 4 (2011) 221-235.Search in Google Scholar

31. Park, S.Y., Bae, D.J., Kim, M.J., Piao, M.L. and Kim, I.S. Extracellular low pH modulates phosphatidylserine-dependent phagocytosis in macrophages by increasing stabilin-1 expression. J. Biol. Chem. 287 (2012) 11261-11271.Search in Google Scholar

32. Meurette, O., Rebillard, A., Huc, L., Le Moigne, G., Merino, D., Micheau, O., Lagadic-Gossman, L. and Dimanche-Boitrel, M-T. TRAIL induces receptorinteracting protein 1-dependent and caspase-dependent necrosis-like cell death under lowextracellular conditions. Cancer Res. 67 (2007) 218-226.Search in Google Scholar

33. Francis, V.G., Majeed, M.A. and Gummadi, S.N. Recovery of functionally active recombinant human phospholipid scramblase 1 from inclusion bodies using N-lauroyl sarcosine. J. Ind. Microbiol. Biotechnol. 39 (2012) 1041-1048.Search in Google Scholar

34. Rajasekharan, A. and Gummadi, S.N. Inhibition of biogenic membrane flippase activity in reconstituted ER proteoliposomes in the presence of low cholesterol levels. Cell. Mol. Biol. Lett. 17 (2012) 136-152.Search in Google Scholar

35. Kim, S., Bae, D-J., Hong, M., Park, S-Y. and Kim, I.S. The conserved histidine in epidermal growth factor-like domains of stabilin-2 modulates pH-dependent recognition of phosphatidylserine in apoptotic cells. Int. J. Biochem. Cell Biol. 42 (2010) 1154-1163.Search in Google Scholar

36. Stout, J. G., Zhou, Q., Wiedmer, T., Sims, P.J. Change in conformation of plasma membrane phospholipid scramblase induced by occupancy of its Ca2+ binding site. Biochemistry 37 (1998) 14860-14866.Search in Google Scholar

37. Li, S., Yang, W., Maniccia, A.W., Barrow, D., Tjong, H., Zhou, H-X. and Yang, J.J. Rational design of a conformation-switchable Ca2+- and Tb3+-binding protein without the use of multiple coupled metal-binding sites. FEBS J. 275 (2008) 5048-5061.Search in Google Scholar

38. Basse, F., Stout, J.G., Sims, P.J. and Wiedmer, T. Isolation of an erythrocyte membrane protein that mediates Ca2+-dependent transbilayer movement of phospholipid. J. Biol. Chem. 271 (1996) 17205-17210.Search in Google Scholar

39. Leventis, P.A. and Grinstein, S. The distribution and function of phosphatidylserine in cellular membranes. Annu. Rev. Biophys. 39 (2010) 407-427.Search in Google Scholar

40. Suzuki, H. and Kanazawa, T. The tryptophan fluorescence change upon conformational transition of the phosphoenzyme intermediate in sarcoplasmic reticulum Ca2+-ATPase is revealed in the absence of K+ and the presence of lasalocid. J. Biol. Chem. 270 (1995) 3089-3093.Search in Google Scholar

41. Donato, R. Calcium-independent, pH-regulated effects of S-100 proteins on assembly-disassembly of brain microtubule protein in vitro. J. Biol. Chem. 263 (1988) 106-110. Search in Google Scholar

42. Lamb, J.A., Allen, P.G., Tuan, B.Y. and Janmey, P.A. Modulation of gelsolin function. Activation at low pH overrides Ca2+ requirement. J. Biol. Chem. 268 (1993) 8999-9004.Search in Google Scholar

43. André, I., Kesvatera, T., Jonsson, B., Akerfeldt, K.S. and Linse, S. The role of electrostatic interactions in calmodulin-peptide complex formation. Biophys. J. 87 (2004) 1929-1938.Search in Google Scholar

44. Haiech, J., Klee, C.B. and Demaille, J.G. Effects of cations on affinity of calmodulin for calcium: ordered binding of calcium ions allows the specific activation of calmodulin-stimulated enzymes. Biochemistry 20 (1981) 3890-3897.Search in Google Scholar

45. Lagarrigue, E., Ternent, D., Maciver, S.K., Fattoum, A., Benyamin, Y. and Roustan, C. The activation of gelsolin by low pH: the calcium latch is sensitive to calcium but not pH. Eur. J. Biochem. 270 (2003) 4105-4112.Search in Google Scholar

46. Baudier, J. and Gerard, D. Ions binding to S100 proteins. II. Conformational studies and calcium-induced conformational changes in S100 alpha alpha protein: the effect of lowpH and calcium incubation on subunit exchange in S100a (alpha beta) protein. J. Biol. Chem. 261 (1986) 8204-8212.Search in Google Scholar

47. Francis, V.G., Mohammed, A.M., Aradhyam, G.K. and Gummadi, S.N. The single C-terminal helix of human phospholipid scramblase 1 is required for membrane insertion and scrambling activity. FEBS J. 280 (2013) 2855-2869.Search in Google Scholar

48. Jones, R.J. and Thompson, C.B. Tumor suppressors and cell metabolism: a recipe for cancer growth. Genes Dev. 23 (2009) 537-548.Search in Google Scholar

49. Wike-Hooley, J.L., Haveman, J. and Reinhold, H.S. The relevance of tumour pH to the treatment of malignant disease. Radiother. Oncol. 2 (1984) 343-366.Search in Google Scholar

50. Park, S.Y., Bae, B-E., Kim, M.J., Piao, M.L. and Kim, I.S. Extracellular low pH modulates phosphatidylserine-dependent phagocytosis in macrophages by increasing stabilin-1 expression. J. Biol. Chem. 287 (2012) 11261-11271.Search in Google Scholar

51. Duggan, S.P., Gallagher, W.M., Fox, E.J.P., Abdel-Latif, M.M., Reynolds, J.V. and Kelleher, D. Low pH induces co-ordinate regulation of gene expression in oesophageal cells. Carcinogenesis 27 (2006) 319-327.Search in Google Scholar

52. Tixier, E., Galmiche, J.P. and Neunlist, M. Acidity induces c-Fos expression in a subpopulation of human colonic submucosal neurons. Neurosci. Lett. 404 (2006) 23-27.Search in Google Scholar

53. Xu, L. and Fidler, I.J. Acidic pH-induced elevation in interleukin 8 expression by human ovarian carcinoma cells. Cancer Res. 60 (2000) 4610-4616.Search in Google Scholar

54. Foletta, V.C., Segal, D.H. and Cohen, D.R. Transcriptional regulation in the immune system: all roads lead to AP-1. J. Leukoc. Biol. 63 (1998) 139-152.10.1002/jlb.63.2.139Search in Google Scholar PubMed

55. Yu, A., McMaster, C.R., Byers, D.M., Ridgway, N.D. and Cook, H.W. Stimulation of phosphatidylserine biosynthesis and facilitation of UV-induced apoptosis in Chinese hamster ovary cells overexpressing phospholipid scramblase 1. J. Biol. Chem. 278 (2003) 9706-9714. Search in Google Scholar

Received: 2014-9-1
Accepted: 2015-1-27
Published Online: 2015-5-15
Published in Print: 2015-6-1

© University of Wrocław, Poland

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