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Apoptosis is required for the proper formation of the ventriculo-arterial connections

M Watanabe1, A Jafri, S A Fisher

  • 1Pediatrics, Case Western Reserve School of Medicine, Cleveland, Ohio 44106, USA.

Developmental Biology
|January 11, 2002
PubMed

Insights

Cardiomyocyte apoptosis is essential for embryonic heart development, driving outflow tract shortening and rotation. Inhibiting apoptosis disrupts cardiac morphogenesis, leading to congenital heart defects.

Area of Science:

  • Developmental Biology
  • Cardiovascular Research
  • Cell Death Mechanisms

Background:

  • Apoptosis (programmed cell death) plays a role in tissue remodeling but its specific function in cardiac morphogenesis is unclear.
  • Cardiomyocyte apoptosis is observed during the embryonic development of the chicken heart's outflow tract (OFT).

Purpose of the Study:

  • To investigate if cardiomyocyte apoptosis is the driving force behind OFT shortening and rotation.
  • To determine if OFT cardiomyocyte apoptosis is necessary for establishing the mature ventriculo-arterial connections.

Main Methods:

  • Chick embryos were treated with caspase inhibitors (zVAD-fmk, DEVD-cho) during critical developmental stages (HH 15-20).
  • Morphological assessments were performed at HH stage 35.
  • Recombinant adenovirus was used to track OFT cardiomyocyte fate and to overexpress the X-linked inhibitor of apoptosis protein (XIAP).

Main Results:

  • Inhibition of apoptosis led to a failure of OFT shortening and rotation, resulting in abnormal great vessel connections and transposition of the aorta.
  • These defects mimicked human congenital double outlet right ventricle.
  • Targeted inhibition of OFT cardiomyocyte apoptosis using XIAP expression produced similar results, while affecting other cardiac structures less.

Conclusions:

  • Elimination of OFT cardiomyocytes via apoptosis is crucial for proper ventriculo-arterial connection formation.
  • Apoptosis is implicated as a potential mechanism underlying congenital conal heart defects caused by teratogens or genetic factors.

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