Trichloroethylene disrupts cardiac gene expression and calcium homeostasis in rat myocytes

Patricia T. Caldwell, Patricia A. Thorne, Paula D. Johnson, Scott A Boitano, Raymond B Runyan, Ornella Selmin

Research output: Contribution to journalArticle

19 Citations (Scopus)

Abstract

We have been investigating the molecular mechanisms by which trichloroethylene (TCE) might induce cardiac malformations in the embryonic heart. Previous results indicated that TCE disrupted expression of genes encoding proteins involved in regulation of intracellular Ca2+, [Ca2+]i, in cardiac cells, including ryanodine receptor isoform 2 (Ryr2), and sarcoendoplasmatic reticulum Ca2+ ATPase, Serca2a. These observations are important in light of the notion that altered cardiac contractility can produce morphological defects. The hypothesis tested in this study is that the TCE-induced changes in gene expression of Ca2+-associated proteins resulted in altered Ca2+ flux regulation. We used real-time PCR and digital imaging microscopy to characterize effects of various doses of TCE on gene expression and Ca2+ response to vasopressin (VP) in rat cardiac H9c2 myocytes. We observed a reduction in Serca2a and Ryr2 expression at 12 and 48 h after exposure to TCE. In addition, we found significant differences in Ca2+ response to VP in cells treated with TCE doses as low as 10 parts per billion. Taken all together, our data strongly indicate that exposure to TCE disrupts the ability of myocytes to regulate cellular Ca2+ fluxes. Perturbation of calcium signaling alters cardiac cell physiology and signal transduction and may hint to morphogenetic consequences in the context of heart development. These results point to a novel area of TCE biology and, if confirmed in vivo, may help to explain the apparent cardio-specific toxicity of TCE exposure in the rodent embryo.

Original languageEnglish (US)
Pages (from-to)135-143
Number of pages9
JournalToxicological Sciences
Volume104
Issue number1
DOIs
StatePublished - Jun 2008

Fingerprint

Trichloroethylene
Gene expression
Muscle Cells
Rats
Homeostasis
Calcium
Gene Expression
Ryanodine Receptor Calcium Release Channel
Vasopressins
Protein Isoforms
Fluxes
Cell Physiological Phenomena
Signal transduction
Reticulum
Gene encoding
Calcium Signaling
Calcium-Transporting ATPases
Physiology
Cardiac Myocytes
Toxicity

Keywords

  • Calcium flux
  • Cardiac development
  • Environmental toxicants
  • Trichloroethylene

ASJC Scopus subject areas

  • Toxicology

Cite this

Trichloroethylene disrupts cardiac gene expression and calcium homeostasis in rat myocytes. / Caldwell, Patricia T.; Thorne, Patricia A.; Johnson, Paula D.; Boitano, Scott A; Runyan, Raymond B; Selmin, Ornella.

In: Toxicological Sciences, Vol. 104, No. 1, 06.2008, p. 135-143.

Research output: Contribution to journalArticle

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