Cellular and molecular mechanisms of single and collective cell migrations in Drosophila: themes and variations.

Annu Rev Genet

Molecular, Cellular and Developmental Biology, University of California, Santa Barbara, California; 93106-9625; email: ,

Published: July 2015

AI Article Synopsis

  • Cell migration is crucial for development and maintaining health, with its dysfunction linked to diseases like cancer and autoimmune issues.
  • Research has shown that while cell migration involves cell polarization and cytoskeletal changes, recent studies highlight the complexity of this process, including the migration of cells in groups rather than individually.
  • Advances in Drosophila genetics, live imaging, and biophysical methods have provided new insights into cell motility, raising new questions about mechanisms like the role of E-Cadherin in migration.

Article Abstract

The process of cell migration is essential throughout life, driving embryonic morphogenesis and ensuring homeostasis in adults. Defects in cell migration are a major cause of human disease, with excessive migration causing autoimmune diseases and cancer metastasis, whereas reduced capacity for migration leads to birth defects and immunodeficiencies. Myriad studies in vitro have established a consensus view that cell migrations require cell polarization, Rho GTPase-mediated cytoskeletal rearrangements, and myosin-mediated contractility. However, in vivo studies later revealed a more complex picture, including the discovery that cells migrate not only as single units but also as clusters, strands, and sheets. In particular, the role of E-Cadherin in cell motility appears to be more complex than previously appreciated. Here, we discuss recent advances achieved by combining the plethora of genetic tools available to the Drosophila geneticist with live imaging and biophysical techniques. Finally, we discuss the emerging themes such studies have revealed and ponder the puzzles that remain to be solved.

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Source
http://dx.doi.org/10.1146/annurev-genet-120213-092218DOI Listing

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