The investigators started with mice that carry the green fluorescent protein (GFP) gene under control of a neuronal promoter, so they could easily see when cells switched on the neuron signal. They isolated embryonic fibroblasts from these mice to test out the iN protocol.

Vierbuchen and colleagues selected 19 candidate genes specific to neural tissues, or involved in neural development or epigenetic reprogramming. They constructed lentiviral vectors for each gene, and then pooled the lot. Next, they used this pool to transform the mouse fibroblasts, reasoning that some subset of the transformed cells would hit upon the right combination to turn neural. A month later, some of the cells had neuronal morphology and GFP fluorescence.

From there, the researchers narrowed down the necessary genes to a set of five: Ascl1, Myt1l, Zic1, Olig2, and Brn2 (also called Pou3f2). Five-factor iN cells expressed neuronal markers including MAP2, GABA, GLUT1, NeuN, and synapsin. Patch-clamp experiments confirmed they were capable of producing action potentials. They were able to form signal-carrying synapses with other neurons as well as with each other.

Finally, Wernig and colleagues further reduced the number of transcription factors necessary to make iN cells by trying all possible three-gene combinations. They settled on a set of Ascl1, Myt1l, and Brn2. These three were able to induce iN formation at up to 19.5 percent efficiency, the authors report. “Generation of iN cells from non-neuronal lineages could have important implications for studies of neural development, neurological disease modeling, and regenerative medicine,” they wrote.—Amber Dance.

Reference:
Vierbuchen T, Ostermeier A, Pang ZP, Kokubu Y, Südhof TC, Wernig M. Direct conversion of fibroblasts to functional neurons by defined factors. Nature. 2010. Abstract