TY - JOUR
T1 - Correlation between cationic lipid-based transfection and cell division
AU - Kirchenbuechler, Inka
AU - Kirchenbuechler, David
AU - Elbaum, Michael
N1 - Publisher Copyright: © 2016.
PY - 2016/7/1
Y1 - 2016/7/1
N2 - We evaluate the temporal relation between protein expression by cationic lipid-mediated transfection and cell division using time lapse fluorescence microscopy. Detailed image analysis provides new insights on the single cell level while simultaneously achieving appropriate statistics. Earlier evidence by less direct methods such as flow cytometry indicates a primary route for transfection involving nuclear envelope breakdown, but also suggests the existence of a pathway independent of mitosis. We confirm and quantify both mechanisms. We found the timing for successful transfection to be unexpectedly flexible, contrary to assertions of a narrow time window. Specifically, cells dividing more than 24 h after exposure to the transfection medium express the probed protein at a comparable level to cells in a mitotic state during or shortly after transfection. This finding can have a profound impact on the guidance and development of non-viral gene delivery materials.
AB - We evaluate the temporal relation between protein expression by cationic lipid-mediated transfection and cell division using time lapse fluorescence microscopy. Detailed image analysis provides new insights on the single cell level while simultaneously achieving appropriate statistics. Earlier evidence by less direct methods such as flow cytometry indicates a primary route for transfection involving nuclear envelope breakdown, but also suggests the existence of a pathway independent of mitosis. We confirm and quantify both mechanisms. We found the timing for successful transfection to be unexpectedly flexible, contrary to assertions of a narrow time window. Specifically, cells dividing more than 24 h after exposure to the transfection medium express the probed protein at a comparable level to cells in a mitotic state during or shortly after transfection. This finding can have a profound impact on the guidance and development of non-viral gene delivery materials.
UR - http://www.scopus.com/inward/record.url?scp=84973473472&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.yexcr.2014.11.019
DO - https://doi.org/10.1016/j.yexcr.2014.11.019
M3 - مقالة
SN - 0014-4827
VL - 345
SP - 1
EP - 5
JO - Experimental Cell Research
JF - Experimental Cell Research
IS - 1
ER -