Measuring cell-edge protrusion dynamics during spreading using live-cell microscopy

Nikola Lukic, Trishna Saha, Stefanie Lapetina, Michal Gendler, Gilad Lehmann, Anthony J. Koleske, Hava Gil-Henn

Research output: Contribution to journalArticlepeer-review

Abstract

The development and homeostasis of multicellular organisms rely on coordinated regulation of cell migration. Cell migration is an essential event in the construction and regeneration of tissues, and is critical in embryonic development, immunological responses, and wound healing. Dysregulation of cell motility contributes to pathological disorders, such as chronic inflammation and cancer metastasis. Cell migration, tissue invasion, axon, and dendrite outgrowth all initiate with actin polymerization-mediated cell-edge protrusions. Here, we describe a simple, efficient, time-saving method for the imaging and quantitative analysis of cell-edge protrusion dynamics during spreading. This method measures discrete features of cell-edge membrane dynamics, such as protrusions, retractions, and ruffles, and can be used to assess how manipulations of key actin regulators impact cell-edge protrusions in diverse contexts.

Original languageEnglish
Article numbere63157
JournalJournal of Visualized Experiments
Volume2021
Issue number177
DOIs
StatePublished - 1 Nov 2021

Bibliographical note

Publisher Copyright:
© 2021 JoVE Journal of Visualized Experiments.

Funding

This work was supported by grants NIH MH115939, NS112121, NS105640, and R56MH122449-01A1 (to Anthony J. Koleske) and from the Israel Science Foundation (grants number 1462/17 and 2142/21) (to Hava Gil-Henn).

FundersFunder number
National Institutes of HealthR56MH122449-01A1, NS105640, NS112121
National Institute of Mental HealthR01MH115939
Israel Science Foundation2142/21, 1462/17

    Fingerprint

    Dive into the research topics of 'Measuring cell-edge protrusion dynamics during spreading using live-cell microscopy'. Together they form a unique fingerprint.

    Cite this