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PMID: 1506433 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Syringe loading introduces macromolecules into living mammalian cell cytosol.

Journal of cell science ·Vol. 102 ( Pt 3) ·1992-07-00 ·Pages 533-41

Clarke MS, McNeil PL

Abstract

We describe a simple, efficient, gentle and inexpensive technique for the introduction of normally impermeant macromolecules into the cytosol of living mammalian cells growing in suspension or attached to the culturing substratum. Loading is achieved by the production of transient, survivable plasma membrane disruptions as cells are passed back and forth through a standard syringe needle or similar narrow orifice. The loading volume required, which contains cells and the macromolecule to be loaded, can be as little as 5 microliters, thus minimizing the use of valuable reagents. In addition, we report that the surfactant molecule, Pluronic F-68, is capable of altering the physical properties of the plasma membrane in such a way as to increase loading efficiency and the long-term survivability of cells loaded by this and other mechanically based cell-loading techniques.

MeSH Terms
3T3 Cells Animals Cattle Cells, Cultured Cytological Techniques Macromolecular Substances Mice Microinjections/methods Poloxalene Syringes
Chemicals
Macromolecular Substances Poloxalene
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Clarke M S
Department of Anatomy and Cellular Biology, Harvard Medical School, Boston, MA 02115.
McNeil P L
Article Info
Journal
Journal of cell science
Abbr.
J Cell Sci
ISSN
0021-9533
Published
1992-07-00
Pages
533-41
Language
English
Region
England
NLM ID
0052457
Subset
IM
Grants
NCI NIH HHS · CA42275 · United States
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