Skip to main content
Log in

Apoptosis in serum-deprived vascular smooth muscle cells: Evidence for cell volume-independent mechanism

  • Published:
Apoptosis Aims and scope Submit manuscript

Abstract

Shrinkage is the earliest hallmark of cells undergoing apoptosis. This study examines the role of this phenomenon in the onset of vascular smooth muscle cell (VSMC) apoptosis triggered by growth factor withdrawal. In hyperosmotic media, VSMC showed the same amplitude of shrinkage but were more resistant to apoptosis than endothelial, epithelial and immune system cells. As with growth factor withdrawal, apoptosis in hyperosmotically-shrunken VSMC was sharply potentiated by transfection with E1A-adenoviral protein and was suppressed by activation of cAMP signaling as well as by the pan-caspase inhibitor z-VAD.fmk. Both cell shrinkage and apoptosis in VSMC-E1A treated with hyperosmotic medium were potentiated under sustained Na+, K+ pump inhibition with ouabain that was in contrast to inhibition of apoptosis documented in ouabain-treated, serum-deprived cells. After 1-hr incubation in serum-deprived medium, VSMC-E1A volume declined by ∼15%. Transfer from hypotonic to control medium decreased VSMC-E1A volume by ∼25% without any induction of apoptosis. Neither swelling in hyposmotic medium nor dissipation of the transmembrane gradient of K+ and major organic osmolytes protected serum-deprived VSMC-E1A from apoptosis. Thus, our results show that similarly to immune system, endothelial and epithelial cells, extensive VSMC shrinkage in hyperosmotic medium leads to the development of apoptosis. In contrast to hyperosmotic medium, the modest cell volume decrease occurring in serum-deprived VSMC does not contribute to triggering of the apoptotic machinery.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Kerr JFR, Wyllie AH, Currie AR. Apoptosis: A basic biological phenomenon with wide-ranging implications in tissue kinetics. Br J Cancer 1972; 26: 239–257.

    Google Scholar 

  2. Bortner CD, Cidlowski JA. A necessary role for cell shrinkage in apoptosis. Biochem Pharmacol 1998; 56: 1549–1559.

    Google Scholar 

  3. Okada Y, Maeno E, Shimizu T, Dezaki K, Wang J, Morishima S. Receptor-mediated control of regulatory volume decrease (RVD) and apoptotic volume decrease (AVD). J Physiol 2001; 532: 3–16.

    Google Scholar 

  4. Maeno E, Ishizaki Y, Kanaseki T, Hazama A, Okada Y. Normotonic cell shrinkage because of disordered volume regulation is an early prerequisite to apoptosis. Proc Natl Acad Sci USA 2000; 97: 9487–9492.

    Google Scholar 

  5. Bortner CD, Cidlowski JA. Absence of volume regulatory mechanisms contributes to the rapid activation of apoptosis in thymocytes. Am J Physiol 1996; 271: C950–C961.

    Google Scholar 

  6. Orlov SN, Thorin-Trescases N, Kotelevtsev SV, Tremblay J, Hamet P. Inversion of the intracellular Na+/K+ ratio blocks apoptosis in vascular smooth muscle at a site upstream of caspase-3. J Biol Chem 1999; 274: 16545–16552.

    Google Scholar 

  7. Malek AM, Goss GG, Jiang L, Izumo S, Alper SL. Mannitol at clinical concentration activates multiple signaling pathways and induces apoptosis in endothelial cells. Stroke 1998; 29: 2631–2640.

    Google Scholar 

  8. Michea L, Ferguson DR, Peters EM, Andrews PM, Kirby MR, Burg MB. Cell cycle delay and apoptosis are induced by high salt and urea in renal medullary cells. Am J Physiol 2000; 278: F209–F218.

    Google Scholar 

  9. Orlov SN, Tremblay J, Hamet P. Cell volume in vascular smooth muscle is regulated by bumetanide-sensitive ion transport. Am J Physiol 1996; 270: C1388–C1397.

    Google Scholar 

  10. Bennett MR, Evan GI, Schwartz SM. Apoptosis of rat vascular smooth muscle cells is regulated by p53-dependent and-independent pathways. Circ Res 1995; 77: 266–273.

    Google Scholar 

  11. Bennett MR, Evan GI, Newby AC. Deregulated expression of the c-myc oncogene abolishes inhibition of proliferation of rat vascular smooth muscle cells by serum reduction, interferongamma, heparin, and cyclic nucleotide analogues and induces apoptosis. Circ Res 1994; 74: 525–536.

    Google Scholar 

  12. Thorin E, Hamilton CA, Dominiczak MH, Reid JL. Chronic exposure of cultured bovine endothelial cells to oxidized LDL abolishes prostacyclin release. Arterioscler Thromb 1994; 14: 453–459.

    Google Scholar 

  13. Gekle M, Wunsch S, Oberleithner H, Silbernagl S. Characterization of two MDCK-cell subtypes as a model system to study principal cell and intercalated cell properties. Pflugers Archiv 1994; 428: 157–162.

    Google Scholar 

  14. Bourcier N, Grygorczyk R, Gekle M, Berthiaume Y, Orlov SN. Purinergic-induced ion current in monolayers of C7-MDCK cells: Role of basolateral and apical ion transporters. J Membr Biol 2002; 186: 131–143.

    Google Scholar 

  15. Orlov SN, Dam TV, Tremblay J, Hamet P. Apoptosis in cultured vascular smooth muscle cells. Role of cell volume decrease. Biochem Biophys Res Commun 1996; 221: 708–715.

    Google Scholar 

  16. Hamet P, Richard L, Dam TV et al. Apoptosis in target organs of hypertension. Hypertension 1995; 26: 642–648.

    Google Scholar 

  17. Orlov SN, Thorin-Trescases N, Dulin NO, et al. Activation of cAMP signaling transiently inhibits apoptosis in vascular smooth muscle cells in a site upstream of caspase 3. Cell Death Differ 1999; 6: 691–672.

    Google Scholar 

  18. Therien AG, Blostien R. Mechanisms of sodium pump regulation. Am J Physiol 2000; 279: C541–C566.

    Google Scholar 

  19. Drewnowska K, BaumgartenCV. Regulation of cellular volume in rabbit ventricular myocytes: Bumetanide, chlorothiazide, and ouabain. Am J Physiol 1991; 260: C122–C131.

    Google Scholar 

  20. Willis JS, Ellory JC. Ouabain-sensitivity: Diversities and disparities. Current Topics in Membranes and Transport 1983; 19: 227–280.

    Google Scholar 

  21. Juhasova M, Blaustein MP. Na+ pump low and high ouabain affinity ? subunit isoforms are differently distributed in cells. Proc Natl Acad Sci USA 1997; 94: 1800–1805.

    Google Scholar 

  22. Orlov SN, Taurin S, Hamet P. The ?1-Na/K pump does not mediate the involvement of ouabain in the development of hypertension in rats. Blood Pressure 2002; 11: 56–62.

    Google Scholar 

  23. Hoffmann EK, Simonsen LO. Membrane mechanisms in volume and pH regulation in vertebrate cells. Physiol Rev 1989; 69: 315–382.

    Google Scholar 

  24. Mongin AA, Orlov SN. Mechanisms of cell volume regulation and possible nature of the cell volume sensor. Pathophysiology 2001; 8(2): 77–88.

    Google Scholar 

  25. Gulbins E, Welsch J, Lepple-Wienhues A, Heinle H, Lang F. Inhibition of Fas-induced apoptotic cell death by osmotic cell shrinkage. Biochem Biophys Res Commun 1997; 236: 517–521.

    Google Scholar 

  26. Kim W, Moon S-O, Sung MJ, et al. Protective effect of adrenomedullin in mannitol-induced apoptosis. Apoptosis 2002; 7: 527–536.

    Google Scholar 

  27. Ohyama H, Yamada T, Watanabe I. Cell volume reduction associated with interphase death in rat thymocytes. Radiat Res 1981; 85: 333–339.

    Google Scholar 

  28. Bortner CD, Hughes FM, Cidlowski JA. A primary role for K+ and Na+ efflux in activation of apoptosis. J Biol Chem 1997; 272: 32436–32442.

    Google Scholar 

  29. Bortner CD, Cidlowski JA. Caspase independent/dependent regulation of K+, cell shrinkage, and mitochondrial membrane potential during lymphocyte apoptosis. J Biol Chem 1999; 274: 21953–21962.

    Google Scholar 

  30. Nobel CSI, Aronson JK, van den Dobbelsteen DJ, Slater AFG. Inhibition of Na+/K+-ATPase may be one mechanism contributing to potassium efflux and cell shrinkage in CD995-induced apoptosis. Apoptosis 200; 5: 153-163.

  31. Wesselborg S, Kabelitz D. Activation-driven death of human T cell clones: Time course kinetics of the induction of cell shrinkage, DNA fragmentatoin, and cell death. Cell Immunol 1993; 148: 234–241.

    Google Scholar 

  32. Beauvais F, Michel L, Dubertret L. Human eosinophils in culture undergo a striking and rapid shrinkage during apoptosis. J Leuc Biol 1995; 57: 851–855.

    Google Scholar 

  33. Benson RSP, Heer S, Dive C, Watson AJM. Characterization of cell volume loss in CEM-C7A cells during dexamethasone-induced apoptosis. Am J Physiol 1996; 270: C1190–C1203.

    Google Scholar 

  34. Xiao AY, Wei L, Xia S, Rothman S, Yu SP. Ionic mechanism of ouabain-induced concurrent apoptosis and necrosis in individual cultured cortical neurones. J Neurosci 2002; 22: 1350–1362.

    Google Scholar 

  35. Lang F, Busch G, Ritter M, et al. Functional significance of cell volume regulatory mechanisms. Physiol Rev 1998; 78: 247–306.

    Google Scholar 

  36. Wu QD, Wang JH, Fennesy F, Redmond HP, Bouchier-Hayes D. Taurine prevents high-glucose-induced human vascular endothelial cell apoptosis. Am J Physiol 1999; 277: C1229–C1238.

    Google Scholar 

  37. Bilney AJ, Murray AW. Pro-and anti-apoptotic effects of K+ in HeLa cells. FEBS Letters 1998; 424: 221–224.

    Google Scholar 

  38. Taurin S, Seyrantepe V, Orlov SN, et al. Proteome analysis and functional expression identify mortalin as an anti-apoptotic gene induced by elevation of [Na+]i/[K+]i ratio in cultured vascular smooth muscle cells. Circ Res 2002; 91: 915–922.

    Google Scholar 

  39. Orlov SN, Taurin S, Thorin-Trescases N, Dulin NO, Tremblay J, Hamet P. Inversion of the intracellular Na+/K+ ratio blocks apoptosis in vascular smooth muscle cells by induction of RNA synthesis. Hypertension 2000; 35: 1062–1068.

    Google Scholar 

  40. Hughes FM, Bortner CD, Purdy GD, Cidlowski JA. Intracellular K+ suppresses the activation of apoptosis in lymphocytes. J Biol Chem 1997; 272: 30567–30576.

    Google Scholar 

  41. Hughes FM, Cidlowski JA. Potassium is a critical regulator of apoptotic enzymes in vitro and in vivo. Adv Enzyme Regul 1999; 39: 151–171.

    Google Scholar 

  42. Dallaporta B, Marchetti P, de Pablo MA, et al. Plasma membrane potential in thymocyte apoptosis. J Immunol 1999; 162: 6534–6542.

    Google Scholar 

  43. Wang L, Xu D, Dai W, Lu L. An ultraviolet-activated K+ channel mediates apoptosis of myeloblastic leukemia cells. J Biol Chem 1999; 274: 3678–3685.

    Google Scholar 

  44. Szabo I, Lepple-Wienhues A, Kaba KN, Zoratti M, Gulbins E, Lang F. Tyrosine kinase-dependent activation of a chloride channel in CD95-induced apoptosis in T-lymphocytes. Proc Natl Acad Sci USA 1998; 95: 6169–6174.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to S. N. Orlov.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Orlov, S.N., Pchejetski, D., Taurin, S. et al. Apoptosis in serum-deprived vascular smooth muscle cells: Evidence for cell volume-independent mechanism. Apoptosis 9, 55–66 (2004). https://doi.org/10.1023/B:APPT.0000012122.47197.03

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/B:APPT.0000012122.47197.03

Navigation