AI Article Synopsis

  • Developmental patterning is crucial for processes like tissue formation and organ size during embryo development, and understanding how it works is a significant goal in developmental biology.
  • Ion-channel-regulated bioelectric signals are important in these patterning mechanisms and have been shown to influence embryonic development, regeneration, and cancer across various organisms.
  • Zebrafish serve as a valuable model for studying bioelectricity because of their unique advantages, such as external development and easy genetic manipulation, allowing researchers to explore the role of ion channels and membrane voltage in developmental processes.

Article Abstract

Developmental patterning is essential for regulating cellular events such as axial patterning, segmentation, tissue formation, and organ size determination during embryogenesis. Understanding the patterning mechanisms remains a central challenge and fundamental interest in developmental biology. Ion-channel-regulated bioelectric signals have emerged as a player of the patterning mechanism, which may interact with morphogens. Evidence from multiple model organisms reveals the roles of bioelectricity in embryonic development, regeneration, and cancers. The Zebrafish model is the second most used vertebrate model, next to the mouse model. The zebrafish model has great potential for elucidating the functions of bioelectricity due to many advantages such as external development, transparent early embryogenesis, and tractable genetics. Here, we review genetic evidence from zebrafish mutants with fin-size and pigment changes related to ion channels and bioelectricity. In addition, we review the cell membrane voltage reporting and chemogenetic tools that have already been used or have great potential to be implemented in zebrafish models. Finally, new perspectives and opportunities for bioelectricity research with zebrafish are discussed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10137051PMC
http://dx.doi.org/10.3390/cells12081148DOI Listing

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