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Disruption of calreticulin-mediated cellular adhesion signaling in the cadmium-induced omphalocele in the chick model

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Abstract

Purpose

Administration of cadmium (Cd) causes omphalocele in the chick embryo. The earliest histological changes in the chick Cd model are the breakdown of adherens junctions (AJs). Calreticulin (CRT) plays a key role in Ca2+ signaling and cell adhesion. Ca2+ signaling in the Cd chick model is known to be altered. The calcium-dependent adhesion molecule, E-cadherin, and its associate, β-catenin, are key components of AJs regulated by CRT. CRT knockouts display omphalocele. We hypothesized that CRT, E-cadherin and β-catenin are downregulated during early embryogenesis in the Cd chick model.

Methods

After 60 h (H) incubation, chicks were harvested 1H, 4H, and 8H post treatment with saline or Cd and divided into controls and Cd. RT-PCR was performed to evaluate mRNA levels of CRT, E-cadherin and β-catenin in the Cd chick model.

Results

The mRNA levels of CRT were significantly decreased in the Cd group at 1H compared to controls (p < 0.05). The mRNA levels of E-cadherin and β-catenin were significantly decreased at 4H in the Cd group compared to controls (p < 0.05). There were no significant differences at 8H.

Conclusion

Downregulation of CRT, E-cadherin and β-catenin genes may cause omphalocele in the Cd chick model by disrupting CRT-mediated Ca2+ signaling and AJs.

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Authors and Affiliations

  1. The Children’s Research Centre, Our Lady’s Children’s Hospital, Dublin 12, Ireland

    Takashi Doi & Prem Puri

  2. School of Medicine and Medical Science, Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin, Ireland

    Takashi Doi, Prem Puri, John Bannigan & Jennifer Thompson

Authors
  1. Takashi Doi
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  2. Prem Puri
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  3. John Bannigan
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  4. Jennifer Thompson
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Correspondence to Prem Puri.

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Doi, T., Puri, P., Bannigan, J. et al. Disruption of calreticulin-mediated cellular adhesion signaling in the cadmium-induced omphalocele in the chick model. Pediatr Surg Int 26, 91–95 (2010). https://doi.org/10.1007/s00383-009-2505-9

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