BMC Molecular and Cell Biology is welcoming contributions to a new Collection entitled Cilia biology and ciliopathies. This Collection aims to assemble high-quality original research articles and methodological advancements that shed light on the intricate biology of primary and motile/multi cilia and the wide array of diseases collectively known as ciliopathies.
Despite the fundamental importance of cilia in cell functionality and human health, many aspects of their biology are still poorly understood. Moreover, defects in ciliary structure, biogenesis, or function are linked to a diverse group of genetic disorders known as ciliopathies, which can affect multiple organ systems and lead to a wide range of health issues including polycystic kidney disease, retinal degeneration, and congenital heart disease.
This Collection seeks to cover the latest advancements in cilia research, from the molecular mechanisms of cilia formation and function to the pathogenesis of ciliopathies, including but not limited to:
- Molecular and cellular mechanisms of ciliogenesis and ciliary function including polarity and positioning
- Advances in understanding ciliary signaling pathways
- Understanding the physics of cilia including flow generation
- The role of cilia in development and tissue homeostasis
- Molecular pathogenesis of ciliopathies, including both primary and motile ciliopathies
- Novel insights into the genetic and epigenetic regulation of ciliary dynamics
- Innovative methodologies for studying cilia and ciliary proteins
- Emerging models for cilia biology
- Possible non-ciliary functions of "classical" cilia proteins
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