The transient transfection of transgenes into oligodendrocytes offers
an important tool for studying the function of proteins during myelin
formation. Currently established procedures, however, have generally r
esulted in low survival rates and low levels of uptake of the transgen
e into primary oligodendrocyte progenitors. We describe an electropora
tion method which yields transient transfection of oligodendrocyte pro
genitors of up to 10-15% of the surviving cells, and provides approxim
ately 10(4) surviving, transfected cells per electroporation reaction.
In recent applications transgene expression persisted as the transfec
ted progenitors progressed through subsequent stages of the oligodendr
ocyte lineage. This technique is expected to facilitate the study of t
he function of key proteins and lipids during the development of prima
ry cultured oligodendrocytes.