Skip to main content
Log in

Volume-Sensitive Chloride Channels are Involved in Maintenance of Basal Cell Volume in Human Acute Lymphoblastic Leukemia Cells

  • Published:
The Journal of Membrane Biology Aims and scope Submit manuscript

Abstract

Chloride channels are expressed ubiquitously in different cells. However, the activation and roles of volume-activated chloride channels under normal isotonic conditions are not clarified, especially in lymphatic cells. In this study, the activation of basal and volume-activated chloride currents and their roles in maintenance of basal cell volume under isotonic conditions were investigated in human acute lymphoblastic leukemia Molt4 cells. The patch-clamp technique and time-lapse image analysis were employed to record whole-cell currents and cell volume changes. Under isotonic conditions, a basal chloride current was recorded. The current was weakly outward-rectified and volume-sensitive and was not inactivated obviously in the observation period. A 47% hypertonic bath solution and the chloride channel blockers NPPB and tamoxifen suppressed the current. Exposure of cells to 47% hypotonic bath solution activated further the basal current. The hypotonicity-activated current possessed properties similar to those of the basal current and was inhibited by NPPB, tamoxifen, ATP and hypertonic bath solution. Furthermore, extracellular hypotonic challenges swelled the cells and induced a regulatory volume decrease (RVD). Extracellular applications of NPPB, tamoxifen and ATP swelled the cells under isotonic conditions and inhibited the RVD induced by hypotonic cell swelling. The results suggest that some volume-activated chloride channels are activated under isotonic conditions, resulting in the appearance of the basal chloride current, which plays an important role in the maintenance of basal cell volume in lymphoblastic leukemia cells. Chloride channels can be activated further to induce a regulatory volume recovery when cells are swollen.

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.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  • Bell PD, Komlosi P, Zhang ZR (2009) ATP as a mediator of macula densa cell signalling. Purinergic Signal 5:461–471

    Article  PubMed  CAS  Google Scholar 

  • Chang QZ, Hu DH, Chen M et al (2006) Neuroprotection of chloride channel blockers against NMDA-induced apoptosis of cultured rat hippocampal neurons. Nan Fang Yi Ke Da Xue Xue Bao 26:158–161

    PubMed  CAS  Google Scholar 

  • Chen L, Wang L, Zhu L et al (2002) Cell cycle-dependent expression of volume-activated chloride currents in nasopharyngeal carcinoma cells. Am J Physiol Cell Physiol 283:C1313–C1323

    PubMed  CAS  Google Scholar 

  • Chen LX, Zhu LY, Jacob TJ et al (2007) Roles of volume-activated Cl currents and regulatory volume decrease in the cell cycle and proliferation in nasopharyngeal carcinoma cells. Cell Prolif 40:253–267

    Article  PubMed  CAS  Google Scholar 

  • d’Anglemont de Tassigny A, Berdeaux A, Souktani R et al (2008) The volume-sensitive chloride channel inhibitors prevent both contractile dysfunction and apoptosis induced by doxorubicin through PI3kinase, Akt and Erk 1/2. Eur J Heart Fail 10:39–46

    Article  PubMed  Google Scholar 

  • Duan D, Winter C, Cowley S et al (1997) Molecular identification of a volume-regulated chloride channel. Nature 390:417–421

    Article  PubMed  CAS  Google Scholar 

  • Dutta AK, Sabirov RZ, Uramoto H et al (2004) Role of ATP-conductive anion channel in ATP release from neonatal rat cardiomyocytes in ischaemic or hypoxic conditions. J Physiol 559:799–812

    PubMed  CAS  Google Scholar 

  • Guan YY, Wang GL, Zhou JG (2006) The ClC-3 Cl channel in cell volume regulation, proliferation and apoptosis in vascular smooth muscle cells. Trends Pharmacol Sci 27:290–296

    Article  PubMed  CAS  Google Scholar 

  • He QF, Wang LW, Mao JW et al (2004) Activation of chloride current and decrease of cell volume by ATP in nasopharyngeal carcinoma cells. Sheng Li Xue Bao 56:691–696

    PubMed  CAS  Google Scholar 

  • Jentsch TJ, Valentin S, Frank W et al (2002) Molecular structure and physiological function of chloride channels. Physiol Rev 82:503–568

    PubMed  CAS  Google Scholar 

  • Lang F, Busch GL, Ritter M et al (1998) Functional significance of cell volume regulatory mechanisms. Physiol Rev 78:247–306

    PubMed  CAS  Google Scholar 

  • Lang F, Foller M, Lang K et al (2007) Cell volume regulatory ion channels in cell proliferation and cell death. Methods Enzymol 428:209–225

    Article  PubMed  Google Scholar 

  • Lazarowski ER, Boucher RC, Harden TK (2000) Constitutive release of ATP and evidence for major contribution of ecto-nucleotide pyrophosphatase and nucleoside diphosphokinase to extracellular nucleotide concentrations. J Biol Chem 275:31061–31068

    Article  PubMed  CAS  Google Scholar 

  • Liu HT, Toychiev AH, Takahashi N et al (2008) Maxi-anion channel as a candidate pathway for osmosensitive ATP release from mouse astrocytes in primary culture. Cell Res 18:558–565

    Article  PubMed  CAS  Google Scholar 

  • Mao J, Wang L, Fan A et al (2007) Blockage of volume-activated chloride channels inhibits migration of nasopharyngeal carcinoma cells. Cell Physiol Biochem 19:249–258

    Article  PubMed  CAS  Google Scholar 

  • Mao J, Chen L, Xu B et al (2009) Volume-activated chloride channels contribute to cell-cycle-dependent regulation of HeLa cell migration. Biochem Pharmacol 77:159–168

    Article  PubMed  CAS  Google Scholar 

  • Praetorius HA, Leipziger J (2009) ATP release from non-excitable cells. Purinergic Signal 5:433–446

    Article  PubMed  CAS  Google Scholar 

  • Pusch M, Neher E (1988) Rates of diffusional exchange between small cells and a measuring patch pipette. Pflugers Arch 411:204–211

    Article  PubMed  CAS  Google Scholar 

  • Sabirov RZ, Okada Y (2005) ATP release via anion channels. Purinergic Signal 1:311–328

    Article  PubMed  CAS  Google Scholar 

  • Shen MR, Droogmans G, Eggermont J et al (2000) Differential expression of volume-regulated anion channels during cell cycle progression of human cervical cancer cells. J Physiol 529:385–394

    Article  PubMed  CAS  Google Scholar 

  • Shirley DG, Vekaria RM, Sevigny J (2009) Ectonucleotidases in the kidney. Purinergic Signal 5:501–511

    Article  PubMed  CAS  Google Scholar 

  • Wang GL, Wang XR, Lin MJ et al (2002a) Deficiency in ClC-3 chloride channels prevents rat aortic smooth muscle cell proliferation. Circ Res 91:E28–E32

    Article  PubMed  CAS  Google Scholar 

  • Wang L, Chen L, Zhu L et al (2002b) Regulatory volume decrease is actively modulated during the cell cycle. J Cell Physiol 193:110–119

    Article  PubMed  CAS  Google Scholar 

  • Wondergem R, Gong W, Monen SH et al (2001) Blocking swelling-activated chloride current inhibits mouse liver cell proliferation. J Physiol 532:661–672

    Article  PubMed  CAS  Google Scholar 

  • Xiong D, Heyman NS, Airey J et al (2010) Cardiac-specific, inducible ClC-3 gene deletion eliminates native volume-sensitive chloride channels and produces myocardial hypertrophy in adult mice. J Mol Cell Cardiol 48:211–219

    Article  PubMed  CAS  Google Scholar 

  • Zhou JG, Ren JL, Qiu QY et al (2005) Regulation of intracellular Cl concentration through volume-regulated ClC-3 chloride channels in A10 vascular smooth muscle cells. J Biol Chem 280:7301–7308

    Article  PubMed  CAS  Google Scholar 

  • Zuo W, Zhu L, Bai Z et al (2009) Chloride channels involve in hydrogen peroxide-induced apoptosis of PC12 cells. Biochem Biophys Res Commun 387:666–670

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

This work was supported by the National Natural Science Foundation of China (30771106, 30870567, 30871267, 90913020 and U0932004).

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Liwei Wang or Lixin Chen.

Additional information

Guozhen Cao and Wanhong Zuo contributed equally to the work.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Cao, G., Zuo, W., Fan, A. et al. Volume-Sensitive Chloride Channels are Involved in Maintenance of Basal Cell Volume in Human Acute Lymphoblastic Leukemia Cells. J Membrane Biol 240, 111–119 (2011). https://doi.org/10.1007/s00232-011-9349-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00232-011-9349-7

Keywords

Navigation