Literature DB >> 1388010

Tributyltin increases cytosolic free Ca2+ concentration in thymocytes by mobilizing intracellular Ca2+, activating a Ca2+ entry pathway, and inhibiting Ca2+ efflux.

S C Chow1, G E Kass, M J McCabe, S Orrenius.   

Abstract

The immunotoxic environmental pollutant tri-n-butyltin (TBT) kills thymocytes by apoptosis through a mechanism that requires an increase in intracellular Ca2+ concentration. The addition of TBT (EC50 = 2 microM) to fura-2-loaded rat thymocytes resulted in a rapid and sustained increase in the cytosolic free Ca2+ concentration ([Ca2+]i) to greater than 1 microM. In nominally Ca(2+)-free medium, TBT slightly but consistently increased thymocyte [Ca2+]i by about 0.11 microM. The subsequent restoration of CaCl2 to the medium resulted in a sustained overshoot in [Ca2+]i; similarly, the addition of MnCl2 produced a rapid decrease in the intracellular fura-2 fluorescence in thymocytes exposed to TBT. The rates of Ca2+ and Mn2+ entry stimulated by TBT were essentially identical to the rates stimulated by 2,5-di-(tert.-butyl)-1,4-benzohydroquinone (tBuBHQ), which has previously been shown to empty the agonist-sensitive endoplasmic reticular Ca2+ store and to stimulate subsequent Ca2+ influx by a capacitative mechanism. The addition of excess [ethylenebis(oxyethylenenitrilo)]tetraacetic acid to thymocytes produced a rapid return to basal [Ca2+]i after tBuBHQ treatment but a similar rapid return to basal [Ca2+]i was not observed after TBT treatment. In addition, TBT produced a marked inhibition of both Ca2+ efflux from the cells and the plasma membrane Ca(2+)-ATPase activity. Also, TBT treatment resulted in a rapid decrease in thymocyte ATP level. Taken together, our results show that TBT increases [Ca2+]i in thymocytes by the combination of intracellular Ca2+ mobilization, stimulation of Ca2+ entry, and inhibition of the Ca2+ efflux process. Furthermore, the ability of TBT to apparently mobilize the tBuBHQ-sensitive intracellular Ca2+ store followed by Ca2+ and Mn2+ entry suggests that the TBT-induced [Ca2+]i increase involves a capacitative type of Ca2+ entry.

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Year:  1992        PMID: 1388010     DOI: 10.1016/0003-9861(92)90105-6

Source DB:  PubMed          Journal:  Arch Biochem Biophys        ISSN: 0003-9861            Impact factor:   4.013


  7 in total

1.  A slow sustained increase in cytosolic Ca2+ levels mediates stalk gene induction by differentiation inducing factor in Dictyostelium.

Authors:  P Schaap; T Nebl; P R Fisher
Journal:  EMBO J       Date:  1996-10-01       Impact factor: 11.598

2.  Differential effects of organotin compounds on voltage-gated potassium currents in lymphocytes and neuroblastoma cells.

Authors:  M Oortgiesen; E Visser; H P Vijverberg; W Seinen
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1996-01       Impact factor: 3.000

3.  Tributyltin interacts with mitochondria and induces cytochrome c release.

Authors:  A Nishikimi; Y Kira; E Kasahara; E F Sato; T Kanno; K Utsumi; M Inoue
Journal:  Biochem J       Date:  2001-06-01       Impact factor: 3.857

4.  Effects of heavy metals on mitogen-activated protein kinase pathways.

Authors:  Masato Matsuoka; Hideki Igisu
Journal:  Environ Health Prev Med       Date:  2002-01       Impact factor: 3.674

5.  Increases in cytosolic calcium ion levels in human natural killer cells in response to butyltin exposure.

Authors:  Rhonda Lane; Sabah O Ghazi; Margaret M Whalen
Journal:  Arch Environ Contam Toxicol       Date:  2009-04-14       Impact factor: 2.804

6.  Caspase-10 is the key initiator caspase involved in tributyltin-mediated apoptosis in human immune cells.

Authors:  Harald F Krug
Journal:  J Toxicol       Date:  2012-01-12

Review 7.  Calcium signaling and cytotoxicity.

Authors:  G E Kass; S Orrenius
Journal:  Environ Health Perspect       Date:  1999-02       Impact factor: 9.031

  7 in total

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