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Updated: Apr 17, 2026

Imaging Cell Shape Change in Living Drosophila Embryos
Published on: March 30, 2011
Dynamin regulates metaphase furrow formation and plasma membrane compartmentalization in the syncytial Drosophila
Richa Rikhy1, Manos Mavrakis2, Jennifer Lippincott-Schwartz3
1Cell Biology and Metabolism Program, NICHD, NIH, Building 18T, 101, 18 Library Drive, Bethesda, MD, USA. Present address: Indian Institute of Science Education and Research, Homi Bhabha Road, Pashan, Pune, 411008, India. lippincj@mail.nih.gov richa@iiserpune.ac.in.
Abstract:
The successive nuclear division cycles in the syncytial Drosophila embryo are accompanied by ingression and regression of plasma membrane furrows, which surround individual nuclei at the embryo periphery, playing a central role in embryo compartmentalization prior to cellularization. Here, we demonstrate that cell cycle changes in dynamin localization and activity at the plasma membrane (PM) regulate metaphase furrow formation and PM organization in the syncytial embryo. Dynamin was localized on short PM furrows during interphase, mediating endocytosis of PM components. Dynamin redistributed off ingressed PM furrows in metaphase, correlating with stabilized PM components and the associated actin regulatory machinery on long furrows. Acute inhibition of dynamin in the temperature sensitive shibire mutant embryo resulted in morphogenetic consequences in the syncytial division cycle. These included inhibition of metaphase furrow ingression, randomization of proteins normally polarized to intercap PM and disruption of the diffusion barrier separating PM domains above nuclei. Based on these findings, we propose that cell cycle changes in dynamin orchestrate recruitment of actin regulatory machinery for PM furrow dynamics during the early mitotic cycles in the Drosophila embryo.
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