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Cell migration by swimming: Drosophila adipocytes as a new in vivo model of adhesion-independent motility

Research output: Contribution to journalArticle

Original languageEnglish
Number of pages7
JournalSeminars in Cell and Developmental Biology
Early online date4 Dec 2019
DOIs
DateAccepted/In press - 15 Nov 2019
DateE-pub ahead of print (current) - 4 Dec 2019

Abstract

Several cell lineages migrate through the developing and adult tissues of our bodies utilising a variety of modes of motility to suit the different substrates and environments they encounter en route to their destinations. Here we describe a novel adhesion-independent mode of single cell locomotion utilised by Drosophila fat body cells – the equivalent of vertebrate adipocytes. Like their human counterpart, these large cells were previously presumed to be immotile. However, in the Drosophila pupa fat body cells appear to be motile and migrate in a directed way towards wounds by peristaltic swimming through the hemolymph. The propulsive force is generated from a wave of cortical actomyosin that travels rearwards along the length of the cell. We discuss how this swimming mode of motility overcomes the physical constraints of microscopic objects moving in fluids, how fat body cells switch on other “motility machinery” to plug the wound on arrival, and whether other cell lineages in Drosophila and other organisms may, under certain circumstances, also adopt swimming as an effective mode of migration.

    Research areas

  • Single cell migration, Adhesion-independent cell migration, Swimming, Fat body cell, Drosophila

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  • Full-text PDF (author’s accepted manuscript)

    Rights statement: This is the author accepted manuscript (AAM). The final published version (version of record) is available online via Elsevier at https://doi.org/10.1016/j.semcdb.2019.11.009 . Please refer to any applicable terms of use of the publisher.

    Accepted author manuscript, 330 KB, PDF document

    Embargo ends: 4/12/20

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    Licence: CC BY-NC-ND

  • Supplementary information PDF

    Rights statement: This is the author accepted manuscript (AAM). The final published version (version of record) is available online via Elsevier at https://doi.org/10.1016/j.semcdb.2019.11.009 . Please refer to any applicable terms of use of the publisher.

    Accepted author manuscript, 6.16 MB, PDF document

    Embargo ends: 4/12/20

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    Licence: CC BY-NC-ND

  • Supplementary information PDF

    Rights statement: This is the author accepted manuscript (AAM). The final published version (version of record) is available online via Elsevier at https://doi.org/10.1016/j.semcdb.2019.11.009 . Please refer to any applicable terms of use of the publisher.

    Accepted author manuscript, 3.03 MB, PDF document

    Embargo ends: 4/12/20

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    Licence: CC BY-NC-ND

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