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Current genetic models for studying congenital heart diseases: Advantages and disadvantages
Ayat Shorbaji1, Peter Natesan Pushparaj2, Sherin Bakhashab1,2
1Biochemistry Department, King Abdulaziz University, Jeddah, Saudi Arabia.
Insights
This review evaluates various animal and stem cell models for studying congenital heart disease (CHD). Understanding these models aids in comprehending CHD pathology and developing effective therapies.
Area of Science:
- Cardiovascular Research
- Developmental Biology
- Genetics
Background:
- Congenital heart disease (CHD) involves structural and functional heart anomalies, with increasing global prevalence due to improved diagnostics.
- Numerous CHD-related genes have been identified, offering insights into molecular mechanisms.
- Understanding CHD requires effective research models.
Purpose of the Study:
- To review and compare the advantages and challenges of diverse in vitro and in vivo models for congenital heart disease research.
- To assess the suitability of various models, including primates, canines, Xenopus, rabbits, chicks, mice, Drosophila, zebrafish, and induced pluripotent stem cells (iPSCs), for studying CHD.
- To guide the selection of appropriate models based on specific research objectives.
Main Methods:
- Comparative analysis of in vitro and in vivo models for congenital heart disease (CHD).
- Evaluation of biological characteristics, disease vulnerability, induction methods, and human comparability of models.
- Inclusion of primates, canines, Xenopus frogs, rabbits, chicks, mice, Drosophila, zebrafish, and induced pluripotent stem cells (iPSCs).
Main Results:
- Each model (primates, canines, Xenopus, rabbits, chicks, mice, Drosophila, zebrafish, iPSCs) presents unique advantages and limitations regarding cost, genetic manipulation, physiological similarity, and technical feasibility.
- Zebrafish offer high gene conservation and cardiac similarity but face antibody cross-reactivity issues.
- iPSCs show potential for gene editing but have structural and stability challenges.
Conclusions:
- Diverse CHD models provide valuable insights into cardiac development, disease simulation, and genetic factor verification.
- Model selection depends on research goals, impacting the understanding of CHD pathology and therapy development.
- Further research utilizing these models is crucial for advancing CHD treatment strategies.
Abstract:
Congenital heart disease (CHD) encompasses a diverse range of structural and functional anomalies that affect the heart and the major blood vessels. Epidemiological studies have documented a global increase in CHD prevalence, which can be attributed to advancements in diagnostic technologies. Extensive research has identified a plethora of CHD-related genes, providing insights into the biochemical pathways and molecular mechanisms underlying this pathological state. In this review, we discuss the advantages and challenges of various In vitro and in vivo CHD models, including primates, canines, Xenopus frogs, rabbits, chicks, mice, Drosophila, zebrafish, and induced pluripotent stem cells (iPSCs). Primates are closely related to humans but are rare and expensive. Canine models are costly but structurally comparable to humans. Xenopus frogs are advantageous because of their generation of many embryos, ease of genetic modification, and cardiac similarity. Rabbits mimic human physiology but are challenging to genetically control. Chicks are inexpensive and simple to handle; however, cardiac events can vary among humans. Mice differ physiologically, while being evolutionarily close and well-resourced. Drosophila has genes similar to those of humans but different heart structures. Zebrafish have several advantages, including high gene conservation in humans and physiological cardiac similarities but limitations in cross-reactivity with mammalian antibodies, gene duplication, and limited embryonic stem cells for reverse genetic methods. iPSCs have the potential for gene editing, but face challenges in terms of 2D structure and genomic stability. CRISPR-Cas9 allows for genetic correction but requires high technical skills and resources. These models have provided valuable knowledge regarding cardiac development, disease simulation, and the verification of genetic factors. This review highlights the distinct features of various models with respect to their biological characteristics, vulnerability to developing specific heart diseases, approaches employed to induce particular conditions, and the comparability of these species to humans. Therefore, the selection of appropriate models is based on research objectives, ultimately leading to an enhanced comprehension of disease pathology and therapy.
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