Delivery of membrane-impermeant fluorescent probes into living neural cell populations by lipotransfer

Kirsten Barber, Renee R. Mala, Mary P. Lambert, Rouzi Qiu, Robert C. MacDonald, William L. Klein*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

33 Scopus citations

Abstract

Use of fluorescent probes to monitor f-actin in living cells typically relies on difficult microinjection procedures. The current work has developed cationic lipotransfer of membrane-impermeant probes as an alternative to microinjection. BODIPY® FL-phallacidin, a fluorescent f-actin probe, was packaged into 40-50 nm cationic liposomes. Packaging, verified by gel filtration, enabled delivery of the probe into living nerve cells and provided an image of f-actin that was identical to that seen in fixed, permeabilized cells. Phallacidin alone did not enter living cells, nor was its uptake stimulated by the presence of empty liposomes. All predicted f-actin structures were fluorescent in living cells, indicating a high efficacy of delivery. Cationic lipotransfer of fluorescent probes was rapid, not disruptive to cells, and delivered a probe en masse to a large sample population. Lipotransfer appears to be a promising alternative to microinjection for introducing membrane-impermeant probes and reagents into living cells.

Original languageEnglish (US)
Pages (from-to)17-20
Number of pages4
JournalNeuroscience Letters
Volume207
Issue number1
DOIs
StatePublished - Mar 22 1996

Funding

This work was supportedb y grants to W.L.K. from NIH, The Alzheimer's Association,a nd The Boothroyd Foundationa, nd by NIH grant R01 NS 30795t o R.C.M.

Keywords

  • Actin
  • Cytoskeleton
  • Intracellular probes
  • Live cell imaging
  • Microinjection
  • Neuron

ASJC Scopus subject areas

  • General Neuroscience

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